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<article article-type="research-article" dtd-version="1.3" xmlns:mml="http://www.w3.org/1998/Math/MathML" xmlns:xlink="http://www.w3.org/1999/xlink" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xml:lang="ru"><front><journal-meta><journal-id journal-id-type="publisher-id">vsp</journal-id><journal-title-group><journal-title xml:lang="ru">Вопросы современной педиатрии</journal-title><trans-title-group xml:lang="en"><trans-title>Current Pediatrics</trans-title></trans-title-group></journal-title-group><issn pub-type="ppub">1682-5527</issn><issn pub-type="epub">1682-5535</issn><publisher><publisher-name>Издательство «ПедиатрЪ»</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="doi">10.15690/vsp.v21i5.2449</article-id><article-id custom-type="elpub" pub-id-type="custom">vsp-3031</article-id><article-categories><subj-group subj-group-type="heading"><subject>Research Article</subject></subj-group><subj-group subj-group-type="section-heading" xml:lang="ru"><subject>ОБЗОРЫ ЛИТЕРАТУРЫ</subject></subj-group><subj-group subj-group-type="section-heading" xml:lang="en"><subject>LITERATURE REVIEW</subject></subj-group></article-categories><title-group><article-title>Инновации в терапевтической коррекции микробиома кожи при атопическом дерматите в детском возрасте</article-title><trans-title-group xml:lang="en"><trans-title>Innovations in Therapeutic Improvement of the Cutaneous Microbiome in Children with Atopic Dermatitis</trans-title></trans-title-group></title-group><contrib-group><contrib contrib-type="author" corresp="yes"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0003-2252-8570</contrib-id><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Мурашкин</surname><given-names>Н. Н.</given-names></name><name name-style="western" xml:lang="en"><surname>Murashkin</surname><given-names>Nikolay N.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Мурашкин Николай Николаевич - доктор медицинских наук, заведующий отделением дерматологии с группой лазерной хирургии, заведующий лабораторией патологии кожи у детей отдела научных исследований в педиатрии НМИЦ здоровья детей, профессор кафедры дерматовенерологии и косметологии ЦГМА, профессор кафедры педиатрии и детской ревматологии ФГАОУ ВО Первый МГМУ им. И.М. Сеченова (Сеченовский Университет).</p><p>119296, Москва, Ломоносовский пр-т, д. 2, стр. 1,  тел.: +7 (495) 967-14-20</p></bio><bio xml:lang="en"><p>Moscow</p></bio><email xlink:type="simple">m_nn2001@mail.ru</email><xref ref-type="aff" rid="aff-1"/></contrib><contrib contrib-type="author" corresp="yes"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0002-4107-4642</contrib-id><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Епишев</surname><given-names>Р. В.</given-names></name><name name-style="western" xml:lang="en"><surname>Epishev</surname><given-names>Roman V.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Москва</p></bio><bio xml:lang="en"><p>Moscow</p></bio><xref ref-type="aff" rid="aff-2"/></contrib><contrib contrib-type="author" corresp="yes"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0002-0081-0981</contrib-id><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Иванов</surname><given-names>Р. А.</given-names></name><name name-style="western" xml:lang="en"><surname>Ivanov</surname><given-names>Roman A.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Москва</p></bio><bio xml:lang="en"><p>Moscow</p></bio><xref ref-type="aff" rid="aff-2"/></contrib><contrib contrib-type="author" corresp="yes"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0002-6034-8231</contrib-id><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Материкин</surname><given-names>А. И.</given-names></name><name name-style="western" xml:lang="en"><surname>Materikin</surname><given-names>Alexander I.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Москва</p></bio><bio xml:lang="en"><p>Moscow</p></bio><xref ref-type="aff" rid="aff-2"/></contrib><contrib contrib-type="author" corresp="yes"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0002-0858-8780</contrib-id><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Опрятин</surname><given-names>Л. А.</given-names></name><name name-style="western" xml:lang="en"><surname>Opryatin</surname><given-names>Leonid A.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Москва</p></bio><bio xml:lang="en"><p>Moscow</p></bio><xref ref-type="aff" rid="aff-2"/></contrib><contrib contrib-type="author" corresp="yes"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0001-6884-5171</contrib-id><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Савелова</surname><given-names>А. А.</given-names></name><name name-style="western" xml:lang="en"><surname>Savelova</surname><given-names>Alena A.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Москва</p></bio><bio xml:lang="en"><p>Moscow</p></bio><xref ref-type="aff" rid="aff-2"/></contrib><contrib contrib-type="author" corresp="yes"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0002-2922-3924</contrib-id><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Нежведилова</surname><given-names>Р. Ю.</given-names></name><name name-style="western" xml:lang="en"><surname>Nezhvedilova</surname><given-names>Roza Y.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Москва</p></bio><bio xml:lang="en"><p>Moscow</p></bio><xref ref-type="aff" rid="aff-2"/></contrib><contrib contrib-type="author" corresp="yes"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0002-8232-8936</contrib-id><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Амбарчян</surname><given-names>Э. Т.</given-names></name><name name-style="western" xml:lang="en"><surname>Ambarchian</surname><given-names>Roza T.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Москва</p></bio><bio xml:lang="en"><p>Moscow</p></bio><xref ref-type="aff" rid="aff-3"/></contrib><contrib contrib-type="author" corresp="yes"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0001-9777-0156</contrib-id><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Федоров</surname><given-names>Д. В.</given-names></name><name name-style="western" xml:lang="en"><surname>Fedorov</surname><given-names>Dmitri V.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Москва</p></bio><bio xml:lang="en"><p>Moscow</p></bio><xref ref-type="aff" rid="aff-2"/></contrib><contrib contrib-type="author" corresp="yes"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0003-4297-4631</contrib-id><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Русакова</surname><given-names>Л. Л.</given-names></name><name name-style="western" xml:lang="en"><surname>Rusakova</surname><given-names>Lyudmila L.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Москва</p></bio><bio xml:lang="en"><p>Moscow</p></bio><xref ref-type="aff" rid="aff-2"/></contrib></contrib-group><aff-alternatives id="aff-1"><aff xml:lang="ru">НМИЦ здоровья детей; Первый МГМУ им. И.М. Сеченова (Сеченовский Университет); ЦГМА Управления делами Президента РФ<country>Россия</country></aff><aff xml:lang="en">National Medical Research Center of Children’s Health; Sechenov First Moscow State Medical University; Central State Medical Academy of Department of Presidential Affairs<country>Russian Federation</country></aff></aff-alternatives><aff-alternatives id="aff-2"><aff xml:lang="ru">НМИЦ здоровья детей<country>Россия</country></aff><aff xml:lang="en">National Medical Research Center of Children’s Health<country>Russian Federation</country></aff></aff-alternatives><aff-alternatives id="aff-3"><aff xml:lang="ru">НИИ педиатрии и охраны здоровья детей НКЦ №2 ФГБНУ РНЦХ им. акад. Б.В. Петровского<country>Россия</country></aff><aff xml:lang="en">Pediatrics and Child Health Research Institute in Petrovsky National Research Centre of Surgery<country>Russian Federation</country></aff></aff-alternatives><pub-date pub-type="collection"><year>2022</year></pub-date><pub-date pub-type="epub"><day>07</day><month>11</month><year>2022</year></pub-date><volume>21</volume><issue>5</issue><fpage>352</fpage><lpage>361</lpage><permissions><copyright-statement>Copyright &amp;#x00A9; Мурашкин Н.Н., Епишев Р.В., Иванов Р.А., Материкин А.И., Опрятин Л.А., Савелова А.А., Нежведилова Р.Ю., Амбарчян Э.Т., Федоров Д.В., Русакова Л.Л., 2022</copyright-statement><copyright-year>2022</copyright-year><copyright-holder xml:lang="ru">Мурашкин Н.Н., Епишев Р.В., Иванов Р.А., Материкин А.И., Опрятин Л.А., Савелова А.А., Нежведилова Р.Ю., Амбарчян Э.Т., Федоров Д.В., Русакова Л.Л.</copyright-holder><copyright-holder xml:lang="en">Murashkin N.N., Epishev R.V., Ivanov R.A., Materikin A.I., Opryatin L.A., Savelova A.A., Nezhvedilova R.Y., Ambarchian R.T., Fedorov D.V., Rusakova L.L.</copyright-holder><license license-type="creative-commons-attribution" xlink:href="https://creativecommons.org/licenses/by/4.0/" xlink:type="simple"><license-p>This work is licensed under a Creative Commons Attribution 4.0 License.</license-p></license></permissions><self-uri xlink:href="https://vsp.spr-journal.ru/jour/article/view/3031">https://vsp.spr-journal.ru/jour/article/view/3031</self-uri><abstract><p>Биопленка является доминирующей формой организации микробиоты кожи, способствующей адгезии и сохранению микроорганизмов в кожном микроокружении, что необходимо для обеспечения функции эпидермального барьера и местной иммуномодуляции. Во время обострения атопического дерматита основным колонизатором участков пораженной кожи становятся Staphylococcus aureus, также в основном образующие биопленку. Рост S. aureus и разрастание биопленки за счет других микробных комменсалов на коже пациентов с атопическим дерматитом ведет к хронической продукции провоспалительных цитокинов и в последующем к нарушению состава микробиома здоровой кожи. Влияние микробной биопленки кожи человека на его здоровье делает микробиоту кожи привлекательной мишенью для терапевтического воздействия при различных кожных заболеваниях.</p></abstract><trans-abstract xml:lang="en"><p>Biofilm is the dominant form of skin microbiota organization that provides adhesion and preservation of microorganisms in the skin micro-environment. It is necessary to ensure epidermal barrier function and local immunomodulation. Staphylococcus aureus becomes the major colonizer of skin lesions in case of atopic dermatitis exacerbation, and it also can form the biofilms. S. aureus growth and biofilm formation due to other microbial commensals on the skin of patients with atopic dermatitis leads to chronic output of pro-inflammatory cytokines and later to abnormalities in healthy skin microbiome. The role of microbial biofilm in human’s health makes the skin microbiota an attractive target for therapeutic intervention in various skin diseases.</p></trans-abstract><kwd-group xml:lang="ru"><kwd>атопический дерматит</kwd><kwd>микробиом</kwd><kwd>биопленка</kwd><kwd>Staphylococcus aureus</kwd><kwd>дети</kwd></kwd-group><kwd-group xml:lang="en"><kwd>atopic dermatitis</kwd><kwd>microbiome</kwd><kwd>biofilm</kwd><kwd>Staphylococcus aureus</kwd><kwd>children</kwd></kwd-group><funding-group xml:lang="ru"><funding-statement>Отсутствует</funding-statement></funding-group><funding-group xml:lang="en"><funding-statement>Not specified</funding-statement></funding-group></article-meta></front><back><ref-list><title>References</title><ref id="cit1"><label>1</label><citation-alternatives><mixed-citation xml:lang="ru">Weidinger S, Beck LA, Bieber T, et al. Atopic dermatitis. Nat Rev Dis Primers. 2018;4(1):1. doi: https://doi.org/10.1038/s41572-018-0001-z</mixed-citation><mixed-citation xml:lang="en">Weidinger S, Beck LA, Bieber T, et al. Atopic dermatitis. Nat Rev Dis Primers. 2018;4(1):1. doi: https://doi.org/10.1038/s41572-018-0001-z</mixed-citation></citation-alternatives></ref><ref id="cit2"><label>2</label><citation-alternatives><mixed-citation xml:lang="ru">Bieber T. Atopic dermatitis. N Engl J Med. 2008;358(14): 1483–1494. doi: https://doi.org/10.1056/NEJMra074081</mixed-citation><mixed-citation xml:lang="en">Bieber T. Atopic dermatitis. N Engl J Med. 2008;358(14): 1483–1494. doi: https://doi.org/10.1056/NEJMra074081</mixed-citation></citation-alternatives></ref><ref id="cit3"><label>3</label><citation-alternatives><mixed-citation xml:lang="ru">Werfel T. The role of leukocytes, keratinocytes, and allergenspecific IgE in the development of atopic dermatitis. J Investig Dermatol. 2009;129(8):1878–1891. doi: https://doi.org/10.1038/jid.2009.71</mixed-citation><mixed-citation xml:lang="en">Werfel T. The role of leukocytes, keratinocytes, and allergenspecific IgE in the development of atopic dermatitis. J Investig Dermatol. 2009;129(8):1878–1891. doi: https://doi.org/10.1038/jid.2009.71</mixed-citation></citation-alternatives></ref><ref id="cit4"><label>4</label><citation-alternatives><mixed-citation xml:lang="ru">Nutten S. Atopic dermatitis: Global epidemiology and risk factors. Ann Nutr Metab. 2015;66 Suppl 1:8–16. doi: https://doi.org/10.1159/000370220</mixed-citation><mixed-citation xml:lang="en">Nutten S. Atopic dermatitis: Global epidemiology and risk factors. Ann Nutr Metab. 2015;66 Suppl 1:8–16. doi: https://doi.org/10.1159/000370220</mixed-citation></citation-alternatives></ref><ref id="cit5"><label>5</label><citation-alternatives><mixed-citation xml:lang="ru">Cork MJ, Danby SG, Vasilopoulos Y, et al. Epidermal barrier dysfunction in atopic dermatitis. J Investig Dermatol. 2009;129(8): 1892–1908. doi: https://doi.org/10.1038/jid.2009.133</mixed-citation><mixed-citation xml:lang="en">Cork MJ, Danby SG, Vasilopoulos Y, et al. Epidermal barrier dysfunction in atopic dermatitis. J Investig Dermatol. 2009;129(8): 1892–1908. doi: https://doi.org/10.1038/jid.2009.133</mixed-citation></citation-alternatives></ref><ref id="cit6"><label>6</label><citation-alternatives><mixed-citation xml:lang="ru">Suárez-Fariñas M, Tintle SJ, Shemer A, et al. Nonlesional atopic dermatitis skin is characterized by broad terminal differentiation defects and variable immune abnormalities. J Allergy Clin Immunol. 2011;127(4):954–964.e1–4. doi: https://doi.org/10.1016/j.jaci.2010.12.1124</mixed-citation><mixed-citation xml:lang="en">Suárez-Fariñas M, Tintle SJ, Shemer A, et al. Nonlesional atopic dermatitis skin is characterized by broad terminal differentiation defects and variable immune abnormalities. J Allergy Clin Immunol. 2011;127(4):954–964.e1–4. doi: https://doi.org/10.1016/j.jaci.2010.12.1124</mixed-citation></citation-alternatives></ref><ref id="cit7"><label>7</label><citation-alternatives><mixed-citation xml:lang="ru">Irvine AD, McLean WHI, Leung DYM. Filaggrin mutations associated with skin and allergic diseases. N Engl J Med. 2011;365(14):1315–1327. doi: https://doi.org/10.1056/NEJMra1011040</mixed-citation><mixed-citation xml:lang="en">Irvine AD, McLean WHI, Leung DYM. Filaggrin mutations associated with skin and allergic diseases. N Engl J Med. 2011;365(14):1315–1327. doi: https://doi.org/10.1056/NEJMra1011040</mixed-citation></citation-alternatives></ref><ref id="cit8"><label>8</label><citation-alternatives><mixed-citation xml:lang="ru">Thyssen JP, Kezic S. Causes of epidermal filaggrin reduction and their role in the pathogenesis of atopic dermatitis. J Allergy Clin Immunol. 2014;134(4):792–799. doi: https://doi.org/10.1016/j.jaci.2014.06.014</mixed-citation><mixed-citation xml:lang="en">Thyssen JP, Kezic S. Causes of epidermal filaggrin reduction and their role in the pathogenesis of atopic dermatitis. J Allergy Clin Immunol. 2014;134(4):792–799. doi: https://doi.org/10.1016/j.jaci.2014.06.014</mixed-citation></citation-alternatives></ref><ref id="cit9"><label>9</label><citation-alternatives><mixed-citation xml:lang="ru">Elias PM. Primary role of barrier dysfunction in the pathogenesis of atopic dermatitis. Exp Dermatol. 2018;27(8):847–851. doi: https://doi.org/10.1111/exd.13693</mixed-citation><mixed-citation xml:lang="en">Elias PM. Primary role of barrier dysfunction in the pathogenesis of atopic dermatitis. Exp Dermatol. 2018;27(8):847–851. doi: https://doi.org/10.1111/exd.13693</mixed-citation></citation-alternatives></ref><ref id="cit10"><label>10</label><citation-alternatives><mixed-citation xml:lang="ru">Nakatsuji T, Gallo RL. The role of the skin microbiome in atopic dermatitis. Ann Allergy Asthma Immunol. 2019;122(3):263–269. doi: https://doi.org/10.1016/j.anai.2018.12.003</mixed-citation><mixed-citation xml:lang="en">Nakatsuji T, Gallo RL. The role of the skin microbiome in atopic dermatitis. Ann Allergy Asthma Immunol. 2019;122(3):263–269. doi: https://doi.org/10.1016/j.anai.2018.12.003</mixed-citation></citation-alternatives></ref><ref id="cit11"><label>11</label><citation-alternatives><mixed-citation xml:lang="ru">Brandwein M, Steinberg D, Meshner S. Microbial biofilms and the human skin microbiome. NPJ Biofilms Microbiomes. 2016;2:3. doi: https://doi.org/10.1038/s41522-016-0004-z</mixed-citation><mixed-citation xml:lang="en">Brandwein M, Steinberg D, Meshner S. Microbial biofilms and the human skin microbiome. NPJ Biofilms Microbiomes. 2016;2:3. doi: https://doi.org/10.1038/s41522-016-0004-z</mixed-citation></citation-alternatives></ref><ref id="cit12"><label>12</label><citation-alternatives><mixed-citation xml:lang="ru">Gallo RL. Human skin is the largest epithelial surface for interaction with microbes. J Investig Dermatol. 2017;137(6): 1213–1214. doi: https://doi.org/10.1016/j.jid.2016.11.045</mixed-citation><mixed-citation xml:lang="en">Gallo RL. Human skin is the largest epithelial surface for interaction with microbes. J Investig Dermatol. 2017;137(6): 1213–1214. doi: https://doi.org/10.1016/j.jid.2016.11.045</mixed-citation></citation-alternatives></ref><ref id="cit13"><label>13</label><citation-alternatives><mixed-citation xml:lang="ru">Gonzalez T, Biagini Myers JM, Herr AB, Khurana Hershey GK. Staphylococcal Biofilms in Atopic Dermatitis. Curr Allergy Asthma Rep. 2017;17:81. doi: https://doi.org/10.1016/j.jid.2016.11.045</mixed-citation><mixed-citation xml:lang="en">Gonzalez T, Biagini Myers JM, Herr AB, Khurana Hershey GK. Staphylococcal Biofilms in Atopic Dermatitis. Curr Allergy Asthma Rep. 2017;17:81. doi: https://doi.org/10.1016/j.jid.2016.11.045</mixed-citation></citation-alternatives></ref><ref id="cit14"><label>14</label><citation-alternatives><mixed-citation xml:lang="ru">Di Domenico EG, Cavallo I, Pontone M, et al. Biofilm producing Salmonella typhi: Chronic colonization and development of gallbladder cancer. Int J Mol Sci. 2017;18(9):1887. doi: https://doi.org/10.3390/ijms18091887</mixed-citation><mixed-citation xml:lang="en">Di Domenico EG, Cavallo I, Pontone M, et al. Biofilm producing Salmonella typhi: Chronic colonization and development of gallbladder cancer. Int J Mol Sci. 2017;18(9):1887. doi: https://doi.org/10.3390/ijms18091887</mixed-citation></citation-alternatives></ref><ref id="cit15"><label>15</label><citation-alternatives><mixed-citation xml:lang="ru">Di Domenico EG, Cavallo I, Pontone M, et al. Biofilm is a Major Virulence Determinant in Bacterial Colonization of Chronic Skin Ulcers Independently from the Multidrug Resistant Phenotype. Int J Mol Sci. 2017;18(5):E1077. doi: https://doi.org/10.3390/ijms18051077</mixed-citation><mixed-citation xml:lang="en">Di Domenico EG, Cavallo I, Pontone M, et al. Biofilm is a Major Virulence Determinant in Bacterial Colonization of Chronic Skin Ulcers Independently from the Multidrug Resistant Phenotype. Int J Mol Sci. 2017;18(5):E1077. doi: https://doi.org/10.3390/ijms18051077</mixed-citation></citation-alternatives></ref><ref id="cit16"><label>16</label><citation-alternatives><mixed-citation xml:lang="ru">Götz F. Staphylococcus and biofilms. Mol Microbiol. 2002;43(6):1367–1378. doi: https://doi.org/10.1046/j.13652958.2002.02827.x</mixed-citation><mixed-citation xml:lang="en">Götz F. Staphylococcus and biofilms. Mol Microbiol. 2002;43(6):1367–1378. doi: https://doi.org/10.1046/j.13652958.2002.02827.x</mixed-citation></citation-alternatives></ref><ref id="cit17"><label>17</label><citation-alternatives><mixed-citation xml:lang="ru">Nakatsuji T, Chen TH, Narala S, et al. Antimicrobials from human skin commensal bacteria protect against Staphylococcus aureus and are deficient in atopic dermatitis. Sci Transl Med. 2017; 9(378):eaah4680. doi: https://doi.org/10.1126/scitranslmed.aah4680</mixed-citation><mixed-citation xml:lang="en">Nakatsuji T, Chen TH, Narala S, et al. Antimicrobials from human skin commensal bacteria protect against Staphylococcus aureus and are deficient in atopic dermatitis. Sci Transl Med. 2017; 9(378):eaah4680. doi: https://doi.org/10.1126/scitranslmed.aah4680</mixed-citation></citation-alternatives></ref><ref id="cit18"><label>18</label><citation-alternatives><mixed-citation xml:lang="ru">Akiyama H, Yamasaki O, Tada J, Arata J. Adherence characteristics and susceptibility to antimicrobial agents of Staphylococcus aureus strains isolated from skin infections and atopic dermatitis. J Dermatol Sci. 2000;23(3):155–160. doi: https://doi.org/10.1016/s0923-1811(00)00070-0</mixed-citation><mixed-citation xml:lang="en">Akiyama H, Yamasaki O, Tada J, Arata J. Adherence characteristics and susceptibility to antimicrobial agents of Staphylococcus aureus strains isolated from skin infections and atopic dermatitis. J Dermatol Sci. 2000;23(3):155–160. doi: https://doi.org/10.1016/s0923-1811(00)00070-0</mixed-citation></citation-alternatives></ref><ref id="cit19"><label>19</label><citation-alternatives><mixed-citation xml:lang="ru">Cho SH, Strickland I, Boguniewicz M, Leung DY. Fibronectin and fibrinogen contribute to the enhanced binding of Staphylococcus aureus to atopic skin. J Allergy Clin Immunol. 2001;108(2): 269–274. doi: https://doi.org/10.1067/mai.2001.117455</mixed-citation><mixed-citation xml:lang="en">Cho SH, Strickland I, Boguniewicz M, Leung DY. Fibronectin and fibrinogen contribute to the enhanced binding of Staphylococcus aureus to atopic skin. J Allergy Clin Immunol. 2001;108(2): 269–274. doi: https://doi.org/10.1067/mai.2001.117455</mixed-citation></citation-alternatives></ref><ref id="cit20"><label>20</label><citation-alternatives><mixed-citation xml:lang="ru">Ikezawa Z, Komori J, Ikezawa Y, et al. A role of Staphylococcus aureus, interleukin-18, nerve growth factor and semaphorin 3A, an axon guidance molecule, in pathogenesis and treatment of atopic dermatitis. Allergy Asthma Immunol Res. 2010;2(4):235–246. doi: https://doi.org/10.4168/aair.2010.2.4.235</mixed-citation><mixed-citation xml:lang="en">Ikezawa Z, Komori J, Ikezawa Y, et al. A role of Staphylococcus aureus, interleukin-18, nerve growth factor and semaphorin 3A, an axon guidance molecule, in pathogenesis and treatment of atopic dermatitis. Allergy Asthma Immunol Res. 2010;2(4):235–246. doi: https://doi.org/10.4168/aair.2010.2.4.235</mixed-citation></citation-alternatives></ref><ref id="cit21"><label>21</label><citation-alternatives><mixed-citation xml:lang="ru">Di Domenico EG, Cavallo I, Bordignon V, et al. Inflammatory cytokines and biofilm production sustain Staphylococcus aureus outgrowth and persistence: A pivotal interplay in the pathogenesis of Atopic Dermatitis. Sci Rep. 2018;8:9573. doi: https://doi.org/10.1038/s41598-018-27421-1</mixed-citation><mixed-citation xml:lang="en">Di Domenico EG, Cavallo I, Bordignon V, et al. Inflammatory cytokines and biofilm production sustain Staphylococcus aureus outgrowth and persistence: A pivotal interplay in the pathogenesis of Atopic Dermatitis. Sci Rep. 2018;8:9573. doi: https://doi.org/10.1038/s41598-018-27421-1</mixed-citation></citation-alternatives></ref><ref id="cit22"><label>22</label><citation-alternatives><mixed-citation xml:lang="ru">Allen HB, Vaze ND, Choi C, et al. The presence and impact of biofilm-producing staphylococci in atopic dermatitis. JAMA Dermatol. 2014;150(3):260–265. doi: https://doi.org/10.1001/jamadermatol.2013.8627</mixed-citation><mixed-citation xml:lang="en">Allen HB, Vaze ND, Choi C, et al. The presence and impact of biofilm-producing staphylococci in atopic dermatitis. JAMA Dermatol. 2014;150(3):260–265. doi: https://doi.org/10.1001/jamadermatol.2013.8627</mixed-citation></citation-alternatives></ref><ref id="cit23"><label>23</label><citation-alternatives><mixed-citation xml:lang="ru">Haque MS, Hailu T, Pritchett E, et al. The oldest new finding in atopic dermatitis: Subclinical miliaria as an origin. JAMA Dermatol. 2013;149(4):436–438. doi: https://doi.org/10.1001/2013.jamadermatol.109</mixed-citation><mixed-citation xml:lang="en">Haque MS, Hailu T, Pritchett E, et al. The oldest new finding in atopic dermatitis: Subclinical miliaria as an origin. JAMA Dermatol. 2013;149(4):436–438. doi: https://doi.org/10.1001/2013.jamadermatol.109</mixed-citation></citation-alternatives></ref><ref id="cit24"><label>24</label><citation-alternatives><mixed-citation xml:lang="ru">Sonesson A, Przybyszewska K, Eriksson S, et al. Identification of bacterial biofilm and the Staphylococcus aureus derived protease, staphopain, on the skin surface of patients with atopic dermatitis. Sci Rep. 2017;7(1):8689. doi: https://doi.org/10.1038/s41598-017-08046-2</mixed-citation><mixed-citation xml:lang="en">Sonesson A, Przybyszewska K, Eriksson S, et al. Identification of bacterial biofilm and the Staphylococcus aureus derived protease, staphopain, on the skin surface of patients with atopic dermatitis. Sci Rep. 2017;7(1):8689. doi: https://doi.org/10.1038/s41598-017-08046-2</mixed-citation></citation-alternatives></ref><ref id="cit25"><label>25</label><citation-alternatives><mixed-citation xml:lang="ru">Geoghegan JA, Irvine AD, Foster TJ. Staphylococcus aureus and Atopic Dermatitis: A Complex and Evolving Relationship. Trends Microbiol. 2018;26(6):484–497. doi: https://doi.org/10.1016/j.tim.2017.11.008</mixed-citation><mixed-citation xml:lang="en">Geoghegan JA, Irvine AD, Foster TJ. Staphylococcus aureus and Atopic Dermatitis: A Complex and Evolving Relationship. Trends Microbiol. 2018;26(6):484–497. doi: https://doi.org/10.1016/j.tim.2017.11.008</mixed-citation></citation-alternatives></ref><ref id="cit26"><label>26</label><citation-alternatives><mixed-citation xml:lang="ru">Grice EA, Kong HH, Conlan S, et al. Topographical and temporal diversity of the human skin microbiome. Science. 2009;324(5931):1190–1192. doi: https://doi.org/10.1126/science.1171700</mixed-citation><mixed-citation xml:lang="en">Grice EA, Kong HH, Conlan S, et al. Topographical and temporal diversity of the human skin microbiome. Science. 2009;324(5931):1190–1192. doi: https://doi.org/10.1126/science.1171700</mixed-citation></citation-alternatives></ref><ref id="cit27"><label>27</label><citation-alternatives><mixed-citation xml:lang="ru">Powers CE, McShane DB, Gilligan PH, et al. Microbiome and pediatric atopic dermatitis. J Dermatol. 2015;42(12):1137–1142. doi: https://doi.org/10.1111/1346-8138.13072</mixed-citation><mixed-citation xml:lang="en">Powers CE, McShane DB, Gilligan PH, et al. Microbiome and pediatric atopic dermatitis. J Dermatol. 2015;42(12):1137–1142. doi: https://doi.org/10.1111/1346-8138.13072</mixed-citation></citation-alternatives></ref><ref id="cit28"><label>28</label><citation-alternatives><mixed-citation xml:lang="ru">Williams MR, Gallo RL. The role of the skin microbiome in atopic dermatitis. Curr Allergy Asthma Rep. 2015;15(11):65. doi: https://doi.org/10.1007/s11882-015-0567-4</mixed-citation><mixed-citation xml:lang="en">Williams MR, Gallo RL. The role of the skin microbiome in atopic dermatitis. Curr Allergy Asthma Rep. 2015;15(11):65. doi: https://doi.org/10.1007/s11882-015-0567-4</mixed-citation></citation-alternatives></ref><ref id="cit29"><label>29</label><citation-alternatives><mixed-citation xml:lang="ru">Oh J, Byrd AL, Deming C, et al. Biogeography and individua lity shape function in the human skin metagenome. Nature. 2014;514(7520):59–64. doi: https://doi.org/10.1038/nature13786</mixed-citation><mixed-citation xml:lang="en">Oh J, Byrd AL, Deming C, et al. Biogeography and individua lity shape function in the human skin metagenome. Nature. 2014;514(7520):59–64. doi: https://doi.org/10.1038/nature13786</mixed-citation></citation-alternatives></ref><ref id="cit30"><label>30</label><citation-alternatives><mixed-citation xml:lang="ru">Lagier JC, Edouard S, Pagnier I, et al. Current and past strategies for bacterial culture in clinical microbiology. Clin Microbiol Rev. 2015;28(1):208–236. doi: https://doi.org/10.1128/CMR.00110-14</mixed-citation><mixed-citation xml:lang="en">Lagier JC, Edouard S, Pagnier I, et al. Current and past strategies for bacterial culture in clinical microbiology. Clin Microbiol Rev. 2015;28(1):208–236. doi: https://doi.org/10.1128/CMR.00110-14</mixed-citation></citation-alternatives></ref><ref id="cit31"><label>31</label><citation-alternatives><mixed-citation xml:lang="ru">Kong HH. Skin microbiome: Genomics-based insights into the diversity and role of skin microbes. Trends Mol Med. 2011;17(6): 320–328. doi: https://doi.org/10.1016/j.molmed.2011.01.013</mixed-citation><mixed-citation xml:lang="en">Kong HH. Skin microbiome: Genomics-based insights into the diversity and role of skin microbes. Trends Mol Med. 2011;17(6): 320–328. doi: https://doi.org/10.1016/j.molmed.2011.01.013</mixed-citation></citation-alternatives></ref><ref id="cit32"><label>32</label><citation-alternatives><mixed-citation xml:lang="ru">Nakatsuji T, Chiang HI, Jiang SB, et al. The microbiome extends to subepidermal compartments of normal skin. Nat Commun. 2013;4:1431. doi: https://doi.org/10.1038/ncomms2441</mixed-citation><mixed-citation xml:lang="en">Nakatsuji T, Chiang HI, Jiang SB, et al. The microbiome extends to subepidermal compartments of normal skin. Nat Commun. 2013;4:1431. doi: https://doi.org/10.1038/ncomms2441</mixed-citation></citation-alternatives></ref><ref id="cit33"><label>33</label><citation-alternatives><mixed-citation xml:lang="ru">Oh J, Byrd AL, Park M, et al. Temporal Stability of the Human Skin Microbiome. Cell. 2016;165(4):854–866. doi: https://doi.org/10.1016/j.cell.2016.04.008</mixed-citation><mixed-citation xml:lang="en">Oh J, Byrd AL, Park M, et al. Temporal Stability of the Human Skin Microbiome. Cell. 2016;165(4):854–866. doi: https://doi.org/10.1016/j.cell.2016.04.008</mixed-citation></citation-alternatives></ref><ref id="cit34"><label>34</label><citation-alternatives><mixed-citation xml:lang="ru">Thomas CL, Fernández-Peñas P. The microbiome and atopic eczema: More than skin deep. Australas J Dermatol. 2017;58(1): 18–24. doi: https://doi.org/10.1111/ajd.12435</mixed-citation><mixed-citation xml:lang="en">Thomas CL, Fernández-Peñas P. The microbiome and atopic eczema: More than skin deep. Australas J Dermatol. 2017;58(1): 18–24. doi: https://doi.org/10.1111/ajd.12435</mixed-citation></citation-alternatives></ref><ref id="cit35"><label>35</label><citation-alternatives><mixed-citation xml:lang="ru">Lee SY, Lee E, Park YM, Hong SJ. Microbiome in the Gut-Skin Axis in Atopic Dermatitis. Allergy Asthma Immunol Res. 2018;10(4): 354–362. doi: https://doi.org/10.4168/aair.2018.10.4.354</mixed-citation><mixed-citation xml:lang="en">Lee SY, Lee E, Park YM, Hong SJ. Microbiome in the Gut-Skin Axis in Atopic Dermatitis. Allergy Asthma Immunol Res. 2018;10(4): 354–362. doi: https://doi.org/10.4168/aair.2018.10.4.354</mixed-citation></citation-alternatives></ref><ref id="cit36"><label>36</label><citation-alternatives><mixed-citation xml:lang="ru">Shi B, Bangayan NJ, Curd E, et al. The skin microbiome is different in pediatric versus adult atopic dermatitis. J Allergy Clin Immunol. 2016;138(4):1233–1236. doi: https://doi.org/10.1016/j.jaci.2016.04.053</mixed-citation><mixed-citation xml:lang="en">Shi B, Bangayan NJ, Curd E, et al. The skin microbiome is different in pediatric versus adult atopic dermatitis. J Allergy Clin Immunol. 2016;138(4):1233–1236. doi: https://doi.org/10.1016/j.jaci.2016.04.053</mixed-citation></citation-alternatives></ref><ref id="cit37"><label>37</label><citation-alternatives><mixed-citation xml:lang="ru">Clausen ML, Edslev SM, Andersen PS, et al. Staphylococcus aureus colonization in atopic eczema and its association with filaggrin gene mutations. Br J Dermatol. 2017;177(5):1394–1400. doi: https://doi.org/10.1111/bjd.15470</mixed-citation><mixed-citation xml:lang="en">Clausen ML, Edslev SM, Andersen PS, et al. Staphylococcus aureus colonization in atopic eczema and its association with filaggrin gene mutations. Br J Dermatol. 2017;177(5):1394–1400. doi: https://doi.org/10.1111/bjd.15470</mixed-citation></citation-alternatives></ref><ref id="cit38"><label>38</label><citation-alternatives><mixed-citation xml:lang="ru">Seite S. Flores GE, Henley JB, et al. Microbiome of affected and unaffected skin of patients with atopic dermatitis before and after emollient treatment. J Drugs Dermatol. 2014;13(11):1365–1372.</mixed-citation><mixed-citation xml:lang="en">Seite S. Flores GE, Henley JB, et al. Microbiome of affected and unaffected skin of patients with atopic dermatitis before and after emollient treatment. J Drugs Dermatol. 2014;13(11):1365–1372.</mixed-citation></citation-alternatives></ref><ref id="cit39"><label>39</label><citation-alternatives><mixed-citation xml:lang="ru">Kim MH, Rho M, Choi JP, et al. A Metagenomic Analysis Provides a Culture-Independent Pathogen Detection for Atopic Dermatitis. Allergy Asthma Immunol Res. 2017;9(5):453–461. doi: https://doi.org/10.4168/aair.2017.9.5.453</mixed-citation><mixed-citation xml:lang="en">Kim MH, Rho M, Choi JP, et al. A Metagenomic Analysis Provides a Culture-Independent Pathogen Detection for Atopic Dermatitis. Allergy Asthma Immunol Res. 2017;9(5):453–461. doi: https://doi.org/10.4168/aair.2017.9.5.453</mixed-citation></citation-alternatives></ref><ref id="cit40"><label>40</label><citation-alternatives><mixed-citation xml:lang="ru">Kobayashi T, Glatz M, Horiuchi K, et al. Dysbiosis and Staphylococcus aureus Colonization Drives Inflammation in Atopic Dermatitis. Immunity. 2015;42(4):756–766. doi: https://doi.org/10.1016/j.immuni.2015.03.014</mixed-citation><mixed-citation xml:lang="en">Kobayashi T, Glatz M, Horiuchi K, et al. Dysbiosis and Staphylococcus aureus Colonization Drives Inflammation in Atopic Dermatitis. Immunity. 2015;42(4):756–766. doi: https://doi.org/10.1016/j.immuni.2015.03.014</mixed-citation></citation-alternatives></ref><ref id="cit41"><label>41</label><citation-alternatives><mixed-citation xml:lang="ru">Nakatsuji T, Chen TH, Two AM, et al. Staphylococcus aureus exploits epidermal barrier defects in atopic dermatitis to trigger cytokine expression. J Investig Dermatol. 2016;136(11):2192–2200. doi: https://doi.org/10.1016/j.jid.2016.05.127</mixed-citation><mixed-citation xml:lang="en">Nakatsuji T, Chen TH, Two AM, et al. Staphylococcus aureus exploits epidermal barrier defects in atopic dermatitis to trigger cytokine expression. J Investig Dermatol. 2016;136(11):2192–2200. doi: https://doi.org/10.1016/j.jid.2016.05.127</mixed-citation></citation-alternatives></ref><ref id="cit42"><label>42</label><citation-alternatives><mixed-citation xml:lang="ru">Kong HH, Oh J, Deming C, et al. Temporal shifts in the skin microbiome associated with disease flares and treatment in children with atopic dermatitis. Genome Res. 2012;22(5):850–859. doi: https://doi.org/10.1101/gr.131029.111</mixed-citation><mixed-citation xml:lang="en">Kong HH, Oh J, Deming C, et al. Temporal shifts in the skin microbiome associated with disease flares and treatment in children with atopic dermatitis. Genome Res. 2012;22(5):850–859. doi: https://doi.org/10.1101/gr.131029.111</mixed-citation></citation-alternatives></ref><ref id="cit43"><label>43</label><citation-alternatives><mixed-citation xml:lang="ru">Chng KR, Tay ASL, Li C, et al. Whole metagenome profiling reveals skin microbiome-dependent susceptibility to atopic dermatitis flare. Nat Microbiol. 2016;1(9):16106. doi: https://doi.org/10.1038/nmicrobiol.2016.106</mixed-citation><mixed-citation xml:lang="en">Chng KR, Tay ASL, Li C, et al. Whole metagenome profiling reveals skin microbiome-dependent susceptibility to atopic dermatitis flare. Nat Microbiol. 2016;1(9):16106. doi: https://doi.org/10.1038/nmicrobiol.2016.106</mixed-citation></citation-alternatives></ref><ref id="cit44"><label>44</label><citation-alternatives><mixed-citation xml:lang="ru">Miajlovic H. Effect of filaggrin breakdown products on growth of and protein expression by Staphylococcus aureus. J Allergy Clin Immunol. 2010;126(6):1184–1190.e3. doi: https://doi.org/10.1016/j.jaci.2010.09.015</mixed-citation><mixed-citation xml:lang="en">Miajlovic H. Effect of filaggrin breakdown products on growth of and protein expression by Staphylococcus aureus. J Allergy Clin Immunol. 2010;126(6):1184–1190.e3. doi: https://doi.org/10.1016/j.jaci.2010.09.015</mixed-citation></citation-alternatives></ref><ref id="cit45"><label>45</label><citation-alternatives><mixed-citation xml:lang="ru">Paller AS, Kong HH, Seed P, et al. The microbiome in patients with atopic dermatitis. J Allergy Clin Immunol. 2019;143(1):26–35. doi: https://doi.org/10.1016/j.jaci.2018.11.015</mixed-citation><mixed-citation xml:lang="en">Paller AS, Kong HH, Seed P, et al. The microbiome in patients with atopic dermatitis. J Allergy Clin Immunol. 2019;143(1):26–35. doi: https://doi.org/10.1016/j.jaci.2018.11.015</mixed-citation></citation-alternatives></ref><ref id="cit46"><label>46</label><citation-alternatives><mixed-citation xml:lang="ru">Iwase T, Uehara Y, Shinji H, et al. Staphylococcus epidermidis Esp inhibits Staphylococcus aureus biofilm formation and nasal colonization. Nature. 2010;465(7296):346–349. doi: https://doi.org/10.1038/nature09074</mixed-citation><mixed-citation xml:lang="en">Iwase T, Uehara Y, Shinji H, et al. Staphylococcus epidermidis Esp inhibits Staphylococcus aureus biofilm formation and nasal colonization. Nature. 2010;465(7296):346–349. doi: https://doi.org/10.1038/nature09074</mixed-citation></citation-alternatives></ref><ref id="cit47"><label>47</label><citation-alternatives><mixed-citation xml:lang="ru">Janek D, Zipperer A, Kulik A, et al. High frequency and diversity of antimicrobial activities produced by nasal Staphylococcus strains against bacterial competitors. PLoS Pathog. 2016;12(8):e1005812. doi: https://doi.org/10.1371/journal.ppat.1005812</mixed-citation><mixed-citation xml:lang="en">Janek D, Zipperer A, Kulik A, et al. High frequency and diversity of antimicrobial activities produced by nasal Staphylococcus strains against bacterial competitors. PLoS Pathog. 2016;12(8):e1005812. doi: https://doi.org/10.1371/journal.ppat.1005812</mixed-citation></citation-alternatives></ref><ref id="cit48"><label>48</label><citation-alternatives><mixed-citation xml:lang="ru">Byrd AL, Deming C, Cassidy SKB, et al. Staphylococcus aureus and Staphylococcus epidermidis strain diversity underlying pediatric atopic dermatitis. Sci Transl Med. 2017;9(397):eaal4651. doi: https://doi.org/10.1126/scitranslmed.aal4651</mixed-citation><mixed-citation xml:lang="en">Byrd AL, Deming C, Cassidy SKB, et al. Staphylococcus aureus and Staphylococcus epidermidis strain diversity underlying pediatric atopic dermatitis. Sci Transl Med. 2017;9(397):eaal4651. doi: https://doi.org/10.1126/scitranslmed.aal4651</mixed-citation></citation-alternatives></ref><ref id="cit49"><label>49</label><citation-alternatives><mixed-citation xml:lang="ru">Fleury OM, McAleer MA, Feuillie C, et al. Clumping factor B promotes adherence of Staphylococcus aureus to corneocytes in atopic dermatitis. Infect Immun. 2017;85(6):e00994-16. doi: https://doi.org/10.1128/IAI.00994-16</mixed-citation><mixed-citation xml:lang="en">Fleury OM, McAleer MA, Feuillie C, et al. Clumping factor B promotes adherence of Staphylococcus aureus to corneocytes in atopic dermatitis. Infect Immun. 2017;85(6):e00994-16. doi: https://doi.org/10.1128/IAI.00994-16</mixed-citation></citation-alternatives></ref><ref id="cit50"><label>50</label><citation-alternatives><mixed-citation xml:lang="ru">Harkins CP, Pettigrew KA, Oravcová K, et al. The microevolution and epidemiology of Staphylococcus aureus colonization during atopic eczema disease flare. J Investig Dermatol. 2018;138(2): 336–343. doi: https://doi.org/10.1016/j.jid.2017.09.023</mixed-citation><mixed-citation xml:lang="en">Harkins CP, Pettigrew KA, Oravcová K, et al. The microevolution and epidemiology of Staphylococcus aureus colonization during atopic eczema disease flare. J Investig Dermatol. 2018;138(2): 336–343. doi: https://doi.org/10.1016/j.jid.2017.09.023</mixed-citation></citation-alternatives></ref><ref id="cit51"><label>51</label><citation-alternatives><mixed-citation xml:lang="ru">Rojo A, Aguinaga A, Monecke S, et al. Staphylococcus aureus genomic pattern and atopic dermatitis: May factors other than superantigens be involved? Eur J Clin Microbiol Infect Dis. 2014;33(4):651–658. doi: https://doi.org/10.1007/s10096-013-2000-z</mixed-citation><mixed-citation xml:lang="en">Rojo A, Aguinaga A, Monecke S, et al. Staphylococcus aureus genomic pattern and atopic dermatitis: May factors other than superantigens be involved? Eur J Clin Microbiol Infect Dis. 2014;33(4):651–658. doi: https://doi.org/10.1007/s10096-013-2000-z</mixed-citation></citation-alternatives></ref><ref id="cit52"><label>52</label><citation-alternatives><mixed-citation xml:lang="ru">Manivasagan P, Venkatesan J, Sivakumar K, Kim SK. Pharmaceutically active secondary metabolites of marine actinobacteria. Microbiol Res. 2014;169(4):262–278. doi: https://doi.org/10.1016/j.micres.2013.07.014</mixed-citation><mixed-citation xml:lang="en">Manivasagan P, Venkatesan J, Sivakumar K, Kim SK. Pharmaceutically active secondary metabolites of marine actinobacteria. Microbiol Res. 2014;169(4):262–278. doi: https://doi.org/10.1016/j.micres.2013.07.014</mixed-citation></citation-alternatives></ref><ref id="cit53"><label>53</label><citation-alternatives><mixed-citation xml:lang="ru">van Drongelen V, Haisma EM, Out-Luiting JJ, et al. Reduced filaggrin expression is accompanied by increased Staphylococcus aureus colonization of epidermal skin models. Clin Exp Allergy. 2014;44(12):1515–1524. doi: https://doi.org/10.1111/cea.12443</mixed-citation><mixed-citation xml:lang="en">van Drongelen V, Haisma EM, Out-Luiting JJ, et al. Reduced filaggrin expression is accompanied by increased Staphylococcus aureus colonization of epidermal skin models. Clin Exp Allergy. 2014;44(12):1515–1524. doi: https://doi.org/10.1111/cea.12443</mixed-citation></citation-alternatives></ref><ref id="cit54"><label>54</label><citation-alternatives><mixed-citation xml:lang="ru">Cai SCS, Chen H, Koh W-P, et al. Filaggrin mutations are associated with recurrent skin infection in Singaporean Chinese patients with atopic dermatitis. Br J Dermatol. 2012;166(1):200–203. doi: https://doi.org/10.1111/j.1365-2133.2011.10541.x</mixed-citation><mixed-citation xml:lang="en">Cai SCS, Chen H, Koh W-P, et al. Filaggrin mutations are associated with recurrent skin infection in Singaporean Chinese patients with atopic dermatitis. Br J Dermatol. 2012;166(1):200–203. doi: https://doi.org/10.1111/j.1365-2133.2011.10541.x</mixed-citation></citation-alternatives></ref><ref id="cit55"><label>55</label><citation-alternatives><mixed-citation xml:lang="ru">Berents TL, Carlsen KCL, Mowinckel P, et al. Skin Barrier Function and Staphylococcus aureus Colonization in Vestibulum Nasi and Fauces in Healthy Infants and Infants with Eczema: A Population-Based Cohort Study. PLoS One. 2015;10(6):e0130145. doi: https://doi.org/10.1371/journal.pone.0130145</mixed-citation><mixed-citation xml:lang="en">Berents TL, Carlsen KCL, Mowinckel P, et al. Skin Barrier Function and Staphylococcus aureus Colonization in Vestibulum Nasi and Fauces in Healthy Infants and Infants with Eczema: A Population-Based Cohort Study. PLoS One. 2015;10(6):e0130145. doi: https://doi.org/10.1371/journal.pone.0130145</mixed-citation></citation-alternatives></ref><ref id="cit56"><label>56</label><citation-alternatives><mixed-citation xml:lang="ru">Imokawa G, Kuno H, Kawai M. Stratum corneum lipids serve as a bound-water modulator. J Investig Dermatol. 1991;96(6):845–851. doi: https://doi.org/10.1111/1523-1747.ep12474562</mixed-citation><mixed-citation xml:lang="en">Imokawa G, Kuno H, Kawai M. Stratum corneum lipids serve as a bound-water modulator. J Investig Dermatol. 1991;96(6):845–851. doi: https://doi.org/10.1111/1523-1747.ep12474562</mixed-citation></citation-alternatives></ref><ref id="cit57"><label>57</label><citation-alternatives><mixed-citation xml:lang="ru">Ishikawa J, Narita H, Kond N, et al. Changes in the ceramide profile of atopic dermatitis patients. J Investig Dermatol. 2010;130(10):2511–2514. doi: https://doi.org/10.1038/jid.2010.161</mixed-citation><mixed-citation xml:lang="en">Ishikawa J, Narita H, Kond N, et al. Changes in the ceramide profile of atopic dermatitis patients. J Investig Dermatol. 2010;130(10):2511–2514. doi: https://doi.org/10.1038/jid.2010.161</mixed-citation></citation-alternatives></ref><ref id="cit58"><label>58</label><citation-alternatives><mixed-citation xml:lang="ru">Jungersted JM, Scheer H, Mempel M, et al. Stratum corneum lipids, skin barrier function and filaggrin mutations in patients with atopic eczema. Allergy. 2010;65(7):911–918. doi: https://doi.org/10.1111/j.1398-9995.2010.02326.x</mixed-citation><mixed-citation xml:lang="en">Jungersted JM, Scheer H, Mempel M, et al. Stratum corneum lipids, skin barrier function and filaggrin mutations in patients with atopic eczema. Allergy. 2010;65(7):911–918. doi: https://doi.org/10.1111/j.1398-9995.2010.02326.x</mixed-citation></citation-alternatives></ref><ref id="cit59"><label>59</label><citation-alternatives><mixed-citation xml:lang="ru">Simpson EL, Chalmers JR, Hanifin JM, et al. Emollient enhancement of the skin barrier from birth offers effective atopic dermatitis prevention. J Allergy Clin Immunol. 2014;134(4):818–823. doi: https://doi.org/10.1016/j.jaci.2014.08.005</mixed-citation><mixed-citation xml:lang="en">Simpson EL, Chalmers JR, Hanifin JM, et al. Emollient enhancement of the skin barrier from birth offers effective atopic dermatitis prevention. J Allergy Clin Immunol. 2014;134(4):818–823. doi: https://doi.org/10.1016/j.jaci.2014.08.005</mixed-citation></citation-alternatives></ref><ref id="cit60"><label>60</label><citation-alternatives><mixed-citation xml:lang="ru">Lee E, Lee S-Y, Kang M-J, et al. Clostridia in the gut and onset of atopic dermatitis via eosinophilic inflammation. Ann Allergy Asthma Immunol. 2016;117:91–92. doi: https://doi.org/10.1016/j.anai.2016.04.019</mixed-citation><mixed-citation xml:lang="en">Lee E, Lee S-Y, Kang M-J, et al. Clostridia in the gut and onset of atopic dermatitis via eosinophilic inflammation. Ann Allergy Asthma Immunol. 2016;117:91–92. doi: https://doi.org/10.1016/j.anai.2016.04.019</mixed-citation></citation-alternatives></ref><ref id="cit61"><label>61</label><citation-alternatives><mixed-citation xml:lang="ru">Song H, Yoo Y, Hwang J, et al. Faecalibacterium prausnitzii subspecies-level dysbiosis in the human gut microbiome underlying atopic dermatitis. J Allergy Clin Immunol. 2016;137(36):852–860. doi: https://doi.org/10.1016/j.jaci.2015.08.021</mixed-citation><mixed-citation xml:lang="en">Song H, Yoo Y, Hwang J, et al. Faecalibacterium prausnitzii subspecies-level dysbiosis in the human gut microbiome underlying atopic dermatitis. J Allergy Clin Immunol. 2016;137(36):852–860. doi: https://doi.org/10.1016/j.jaci.2015.08.021</mixed-citation></citation-alternatives></ref><ref id="cit62"><label>62</label><citation-alternatives><mixed-citation xml:lang="ru">O’Neill CA, Monteleone G, McLaughlin JT, Paus R. The gut-skin axis in health and disease: A paradigm with therapeutic implications. Bioessays. 2016;38(11):1167–1176. doi: https://doi.org/10.1002/bies.201600008</mixed-citation><mixed-citation xml:lang="en">O’Neill CA, Monteleone G, McLaughlin JT, Paus R. The gut-skin axis in health and disease: A paradigm with therapeutic implications. Bioessays. 2016;38(11):1167–1176. doi: https://doi.org/10.1002/bies.201600008</mixed-citation></citation-alternatives></ref><ref id="cit63"><label>63</label><citation-alternatives><mixed-citation xml:lang="ru">Salem I, Ramser A, Isham N, Ghannoum MA. The Gut Microbiome as a Major Regulator of the Gut-Skin Axis. Front Microbiol. 2018;9:1459. doi: https://doi.org/10.3389/fmicb.2018.01459</mixed-citation><mixed-citation xml:lang="en">Salem I, Ramser A, Isham N, Ghannoum MA. The Gut Microbiome as a Major Regulator of the Gut-Skin Axis. Front Microbiol. 2018;9:1459. doi: https://doi.org/10.3389/fmicb.2018.01459</mixed-citation></citation-alternatives></ref><ref id="cit64"><label>64</label><citation-alternatives><mixed-citation xml:lang="ru">Kirjavainen PV, Arvola T, Salminen SJ, Isolauri E. Aberrant composition of gut microbiota of allergic infants: A target of bifidobacterial therapy at weaning? Gut. 2002;51(1):51–55. doi: https://doi.org/10.1136/gut.51.1.51</mixed-citation><mixed-citation xml:lang="en">Kirjavainen PV, Arvola T, Salminen SJ, Isolauri E. Aberrant composition of gut microbiota of allergic infants: A target of bifidobacterial therapy at weaning? Gut. 2002;51(1):51–55. doi: https://doi.org/10.1136/gut.51.1.51</mixed-citation></citation-alternatives></ref><ref id="cit65"><label>65</label><citation-alternatives><mixed-citation xml:lang="ru">Abrahamsson TR, Jakobsson HE, Andersson AF, et al. Low diversity of the gut microbiota in infants with atopic eczema. J Allergy Clin Immunol. 2012;129(2):434–440. doi: https://doi.org/10.1016/j.jaci.2011.10.025</mixed-citation><mixed-citation xml:lang="en">Abrahamsson TR, Jakobsson HE, Andersson AF, et al. Low diversity of the gut microbiota in infants with atopic eczema. J Allergy Clin Immunol. 2012;129(2):434–440. doi: https://doi.org/10.1016/j.jaci.2011.10.025</mixed-citation></citation-alternatives></ref><ref id="cit66"><label>66</label><citation-alternatives><mixed-citation xml:lang="ru">Nylund L, Nermes M, Isolauri E, et al. Severity of atopic disease inversely correlates with intestinal microbiota diversity and butyrate-producing bacteria. Allergy. 2015;70(2):241–244. doi: https://doi.org/10.1111/all.12549</mixed-citation><mixed-citation xml:lang="en">Nylund L, Nermes M, Isolauri E, et al. Severity of atopic disease inversely correlates with intestinal microbiota diversity and butyrate-producing bacteria. Allergy. 2015;70(2):241–244. doi: https://doi.org/10.1111/all.12549</mixed-citation></citation-alternatives></ref><ref id="cit67"><label>67</label><citation-alternatives><mixed-citation xml:lang="ru">Lone AG, Atci E, Renslow R, et al. Staphylococcus aureus induces hypoxia and cellular damage in porcine dermal explants. Infect Immun. 2015;83:2531–2541. doi: https://doi.org/10.1128/iAI.03075-14</mixed-citation><mixed-citation xml:lang="en">Lone AG, Atci E, Renslow R, et al. Staphylococcus aureus induces hypoxia and cellular damage in porcine dermal explants. Infect Immun. 2015;83:2531–2541. doi: https://doi.org/10.1128/iAI.03075-14</mixed-citation></citation-alternatives></ref><ref id="cit68"><label>68</label><citation-alternatives><mixed-citation xml:lang="ru">McAleer MA, Irvine AD. The multifunctional role of filaggrin in allergic skin disease. J Allergy Clin Immunol. 2013;131(2):280–291. doi: https://doi.org/10.1016/j.jaci.2012.12.668</mixed-citation><mixed-citation xml:lang="en">McAleer MA, Irvine AD. The multifunctional role of filaggrin in allergic skin disease. J Allergy Clin Immunol. 2013;131(2):280–291. doi: https://doi.org/10.1016/j.jaci.2012.12.668</mixed-citation></citation-alternatives></ref><ref id="cit69"><label>69</label><citation-alternatives><mixed-citation xml:lang="ru">Egawa G, Kabashima K. Multifactorial skin barrier deficiency and atopic dermatitis: Essential topics to prevent the atopic march. J Allergy Clin Immunol. 2016;138(2):350–358.e1. doi: https://doi.org/10.1016/j.jaci.2016.06.002</mixed-citation><mixed-citation xml:lang="en">Egawa G, Kabashima K. Multifactorial skin barrier deficiency and atopic dermatitis: Essential topics to prevent the atopic march. J Allergy Clin Immunol. 2016;138(2):350–358.e1. doi: https://doi.org/10.1016/j.jaci.2016.06.002</mixed-citation></citation-alternatives></ref><ref id="cit70"><label>70</label><citation-alternatives><mixed-citation xml:lang="ru">Kezic S, Kemperman PM, Koster ES, et al. Loss-of-function mutations in the filaggrin gene lead to reduced level of natural moisturizing factor in the stratum corneum. J Investig Dermatol. 2008;128(8):2117–2119. doi: https://doi.org/10.1038/jid.2008.29</mixed-citation><mixed-citation xml:lang="en">Kezic S, Kemperman PM, Koster ES, et al. Loss-of-function mutations in the filaggrin gene lead to reduced level of natural moisturizing factor in the stratum corneum. J Investig Dermatol. 2008;128(8):2117–2119. doi: https://doi.org/10.1038/jid.2008.29</mixed-citation></citation-alternatives></ref><ref id="cit71"><label>71</label><citation-alternatives><mixed-citation xml:lang="ru">Rippke F, Schreiner V, Doering T, Maibach HI. Stratum corneum pH in atopic dermatitis: Impact on skin barrier function and colonization with Staphylococcus aureus. Am J Clin Dermatol. 2004;5(4):217–223. doi: https://doi.org/10.2165/00128071-200405040-00002</mixed-citation><mixed-citation xml:lang="en">Rippke F, Schreiner V, Doering T, Maibach HI. Stratum corneum pH in atopic dermatitis: Impact on skin barrier function and colonization with Staphylococcus aureus. Am J Clin Dermatol. 2004;5(4):217–223. doi: https://doi.org/10.2165/00128071-200405040-00002</mixed-citation></citation-alternatives></ref><ref id="cit72"><label>72</label><citation-alternatives><mixed-citation xml:lang="ru">Weinrick B, Dunman PM, McAleese F, et al. Effect of mild acid on gene expression in Staphylococcus aureus. J Bacteriol. 2004;186(24):8407–8423. doi: https://doi.org/10.1128/jB.186.24.8407-8423.2004</mixed-citation><mixed-citation xml:lang="en">Weinrick B, Dunman PM, McAleese F, et al. Effect of mild acid on gene expression in Staphylococcus aureus. J Bacteriol. 2004;186(24):8407–8423. doi: https://doi.org/10.1128/jB.186.24.8407-8423.2004</mixed-citation></citation-alternatives></ref><ref id="cit73"><label>73</label><citation-alternatives><mixed-citation xml:lang="ru">Huang B, Liu FF, Dong XY, Sun Y. Molecular mechanism of the effects of salt and pH on the affinity between protein A and human immunoglobulin G1 revealed by molecular simulations. J Phys Chem B. 2012;116(1):424–433. doi: https://doi.org/10.1021/jp205770p</mixed-citation><mixed-citation xml:lang="en">Huang B, Liu FF, Dong XY, Sun Y. Molecular mechanism of the effects of salt and pH on the affinity between protein A and human immunoglobulin G1 revealed by molecular simulations. J Phys Chem B. 2012;116(1):424–433. doi: https://doi.org/10.1021/jp205770p</mixed-citation></citation-alternatives></ref><ref id="cit74"><label>74</label><citation-alternatives><mixed-citation xml:lang="ru">Messina JA, Thaden JT, Sharma-Kuinkel BK, Fowler VG. Impact of Bacterial and Human Genetic Variation on Staphylococcus aureus Infections. PLoS Pathog. 2016;12(1):e1005330. doi: https://doi.org/10.1371/journal.ppat.1005330</mixed-citation><mixed-citation xml:lang="en">Messina JA, Thaden JT, Sharma-Kuinkel BK, Fowler VG. Impact of Bacterial and Human Genetic Variation on Staphylococcus aureus Infections. PLoS Pathog. 2016;12(1):e1005330. doi: https://doi.org/10.1371/journal.ppat.1005330</mixed-citation></citation-alternatives></ref><ref id="cit75"><label>75</label><citation-alternatives><mixed-citation xml:lang="ru">Tasse J, Trouillet-Assant S, Josse J, et al. Association between biofilm formation phenotype and clonal lineage in Staphylococcus aureus strains from bone and joint infections. PLoS One. 2018;13(8):e0200064. doi: https://doi.org/10.1371/journal.pone.0200064</mixed-citation><mixed-citation xml:lang="en">Tasse J, Trouillet-Assant S, Josse J, et al. Association between biofilm formation phenotype and clonal lineage in Staphylococcus aureus strains from bone and joint infections. PLoS One. 2018;13(8):e0200064. doi: https://doi.org/10.1371/journal.pone.0200064</mixed-citation></citation-alternatives></ref><ref id="cit76"><label>76</label><citation-alternatives><mixed-citation xml:lang="ru">Croes S, Deurenberg RH, Boumans ML, et al. Staphylococcus aureus biofilm formation at the physiologic glucose concentration depends on the S. aureus lineage. BMC Microbiol. 2009;9:229. doi: https://doi.org/10.1186/1471-2180-9-229</mixed-citation><mixed-citation xml:lang="en">Croes S, Deurenberg RH, Boumans ML, et al. Staphylococcus aureus biofilm formation at the physiologic glucose concentration depends on the S. aureus lineage. BMC Microbiol. 2009;9:229. doi: https://doi.org/10.1186/1471-2180-9-229</mixed-citation></citation-alternatives></ref><ref id="cit77"><label>77</label><citation-alternatives><mixed-citation xml:lang="ru">Akiyama H, Hamada T, Huh WK, et al. Confocal laser scanning microscopic observation of glycocalyx production by Staphylococcus aureus in skin lesions of bullous impetigo, atopic dermatitis and pemphigus foliaceus. Br J Dermatol. 2003;148(3):526–532. doi: https://doi.org/10.1046/j.1365-2133.2003.05162.x</mixed-citation><mixed-citation xml:lang="en">Akiyama H, Hamada T, Huh WK, et al. Confocal laser scanning microscopic observation of glycocalyx production by Staphylococcus aureus in skin lesions of bullous impetigo, atopic dermatitis and pemphigus foliaceus. Br J Dermatol. 2003;148(3):526–532. doi: https://doi.org/10.1046/j.1365-2133.2003.05162.x</mixed-citation></citation-alternatives></ref><ref id="cit78"><label>78</label><citation-alternatives><mixed-citation xml:lang="ru">Pascolini C, Sinagra J, Pecetta S, et al. Molecular and immunological characterization of Staphylococcus aureus in pediatric atopic dermatitis: Implications for prophylaxis and clinical management. Clin Dev Immunol. 2011;2011:718708. doi: https://doi.org/10.1155/2011/718708</mixed-citation><mixed-citation xml:lang="en">Pascolini C, Sinagra J, Pecetta S, et al. Molecular and immunological characterization of Staphylococcus aureus in pediatric atopic dermatitis: Implications for prophylaxis and clinical management. Clin Dev Immunol. 2011;2011:718708. doi: https://doi.org/10.1155/2011/718708</mixed-citation></citation-alternatives></ref><ref id="cit79"><label>79</label><citation-alternatives><mixed-citation xml:lang="ru">Eriksson S, van der Plas MJA, Mörgelin M, Sonesson A. Antibacterial and antibiofilm effects of sodium hypochlorite against Staphylococcus aureus isolates derived from patients with atopic dermatitis. Br J Dermatol. 2017;177(2):513–521. doi: https://doi.org/10.1111/bjd.15410</mixed-citation><mixed-citation xml:lang="en">Eriksson S, van der Plas MJA, Mörgelin M, Sonesson A. Antibacterial and antibiofilm effects of sodium hypochlorite against Staphylococcus aureus isolates derived from patients with atopic dermatitis. Br J Dermatol. 2017;177(2):513–521. doi: https://doi.org/10.1111/bjd.15410</mixed-citation></citation-alternatives></ref><ref id="cit80"><label>80</label><citation-alternatives><mixed-citation xml:lang="ru">Huang JT, Abrams M, Tlougan B, et al. Treatment of Staphylococcus aureus colonization in atopic dermatitis decreases disease severity. Pediatrics. 2009;123(5):e808–e814. doi: https://doi.org/10.1542/peds.2008-2217</mixed-citation><mixed-citation xml:lang="en">Huang JT, Abrams M, Tlougan B, et al. Treatment of Staphylococcus aureus colonization in atopic dermatitis decreases disease severity. Pediatrics. 2009;123(5):e808–e814. doi: https://doi.org/10.1542/peds.2008-2217</mixed-citation></citation-alternatives></ref><ref id="cit81"><label>81</label><citation-alternatives><mixed-citation xml:lang="ru">Wong SM, Ng TG, Baba R. Efficacy and safety of sodium hypochlorite (bleach) baths in patients with moderate to severe atopic dermatitis in Malaysia. J Dermatol. 2013;40(11):874–880. doi: https://doi.org/10.1111/1346-8138.12265</mixed-citation><mixed-citation xml:lang="en">Wong SM, Ng TG, Baba R. Efficacy and safety of sodium hypochlorite (bleach) baths in patients with moderate to severe atopic dermatitis in Malaysia. J Dermatol. 2013;40(11):874–880. doi: https://doi.org/10.1111/1346-8138.12265</mixed-citation></citation-alternatives></ref><ref id="cit82"><label>82</label><citation-alternatives><mixed-citation xml:lang="ru">Gilani SJ, Gonzalez M, Hussain I, et al. Staphylococcus aureus re-colonization in atopic dermatitis: Beyond the skin. Clin Exp Dermatol. 2005;30(1):10–13. doi: https://doi.org/10.1111/j.1365-2230.2004.01679.x</mixed-citation><mixed-citation xml:lang="en">Gilani SJ, Gonzalez M, Hussain I, et al. Staphylococcus aureus re-colonization in atopic dermatitis: Beyond the skin. Clin Exp Dermatol. 2005;30(1):10–13. doi: https://doi.org/10.1111/j.1365-2230.2004.01679.x</mixed-citation></citation-alternatives></ref><ref id="cit83"><label>83</label><citation-alternatives><mixed-citation xml:lang="ru">Friedman BC, Goldman RD. Anti-staphylococcal treatment in dermatitis. Can Fam Physician. 2011;57(6):669–671.</mixed-citation><mixed-citation xml:lang="en">Friedman BC, Goldman RD. Anti-staphylococcal treatment in dermatitis. Can Fam Physician. 2011;57(6):669–671.</mixed-citation></citation-alternatives></ref><ref id="cit84"><label>84</label><citation-alternatives><mixed-citation xml:lang="ru">Fux C, Wilson S, Stoodley P. Detachment characteristics and oxacillin resistance of Staphylococcus aureus biofilm emboli in an in vitro catheter infection model. J Bacteriol. 2004;186(14):4486–4491. doi: https://doi.org/10.1128/JB.186.14.4486-4491.2004</mixed-citation><mixed-citation xml:lang="en">Fux C, Wilson S, Stoodley P. Detachment characteristics and oxacillin resistance of Staphylococcus aureus biofilm emboli in an in vitro catheter infection model. J Bacteriol. 2004;186(14):4486–4491. doi: https://doi.org/10.1128/JB.186.14.4486-4491.2004</mixed-citation></citation-alternatives></ref><ref id="cit85"><label>85</label><citation-alternatives><mixed-citation xml:lang="ru">Girard LP, Ceri H, Gibb AP, et al. MIC Versus MBEC to determine the antibiotic sensitivity of Staphylococcus aureus in peritoneal dialysis peritonitis. Perit Dial Int. 2010;30(6):652–656. doi: https://doi.org/10.3747/pdi.2010.00010</mixed-citation><mixed-citation xml:lang="en">Girard LP, Ceri H, Gibb AP, et al. MIC Versus MBEC to determine the antibiotic sensitivity of Staphylococcus aureus in peritoneal dialysis peritonitis. Perit Dial Int. 2010;30(6):652–656. doi: https://doi.org/10.3747/pdi.2010.00010</mixed-citation></citation-alternatives></ref><ref id="cit86"><label>86</label><citation-alternatives><mixed-citation xml:lang="ru">Castaneda P, McLaren A, Tavaziva G, Overstreet D. Biofilm Antimicrobial Susceptibility Increases with Antimicrobial Exposure Time. Clin Orthop Relat Res. 2016;474(7):1659–1664. doi: https://doi.org/10.1007/s11999-016-4700-z</mixed-citation><mixed-citation xml:lang="en">Castaneda P, McLaren A, Tavaziva G, Overstreet D. Biofilm Antimicrobial Susceptibility Increases with Antimicrobial Exposure Time. Clin Orthop Relat Res. 2016;474(7):1659–1664. doi: https://doi.org/10.1007/s11999-016-4700-z</mixed-citation></citation-alternatives></ref><ref id="cit87"><label>87</label><citation-alternatives><mixed-citation xml:lang="ru">Dawgul M, Baranska-Rybak W, Piechowicz L, et al. The Antistaphylococcal Activity of Citropin 1.1 and Temporin A against Planktonic Cells and Biofilms Formed by Isolates from Patients with Atopic Dermatitis: An Assessment of Their Potential to Induce Microbial Resistance Compared to Conventional Antimicrobials. Pharmaceuticals. 2016;9(2):30. doi: https://doi.org/10.3390/ph9020030</mixed-citation><mixed-citation xml:lang="en">Dawgul M, Baranska-Rybak W, Piechowicz L, et al. The Antistaphylococcal Activity of Citropin 1.1 and Temporin A against Planktonic Cells and Biofilms Formed by Isolates from Patients with Atopic Dermatitis: An Assessment of Their Potential to Induce Microbial Resistance Compared to Conventional Antimicrobials. Pharmaceuticals. 2016;9(2):30. doi: https://doi.org/10.3390/ph9020030</mixed-citation></citation-alternatives></ref><ref id="cit88"><label>88</label><citation-alternatives><mixed-citation xml:lang="ru">Matlow A, Forgie S, Pelude L, et al. Canadian Nosocomial Infection Surveillance Program. Canadian Nosocomial Infection Surveillance Program. National surveillance of methicillinresistant Staphylococcus aureus among hospitalized pediatric patients in Canadian acute care facilities, 1995–2007. Pediatr Infect Dis J. 2012;31(8):814–820. doi: https://doi.org/10.1097/iNF.0b013e31825c48a0</mixed-citation><mixed-citation xml:lang="en">Matlow A, Forgie S, Pelude L, et al. Canadian Nosocomial Infection Surveillance Program. Canadian Nosocomial Infection Surveillance Program. National surveillance of methicillinresistant Staphylococcus aureus among hospitalized pediatric patients in Canadian acute care facilities, 1995–2007. Pediatr Infect Dis J. 2012;31(8):814–820. doi: https://doi.org/10.1097/iNF.0b013e31825c48a0</mixed-citation></citation-alternatives></ref><ref id="cit89"><label>89</label><citation-alternatives><mixed-citation xml:lang="ru">Howlin RP, Brayford MJ, Webb JS, et al. Antibiotic-loaded synthetic calcium sulfate beads for prevention of bacterial colonization and bio film formation in periprosthetic infections. Antimicrob Agents Che mother. 2015;59(1):111–120. doi: https://doi.org/10.1128/AAC.03676-14</mixed-citation><mixed-citation xml:lang="en">Howlin RP, Brayford MJ, Webb JS, et al. Antibiotic-loaded synthetic calcium sulfate beads for prevention of bacterial colonization and bio film formation in periprosthetic infections. Antimicrob Agents Che mother. 2015;59(1):111–120. doi: https://doi.org/10.1128/AAC.03676-14</mixed-citation></citation-alternatives></ref><ref id="cit90"><label>90</label><citation-alternatives><mixed-citation xml:lang="ru">Bhattacharya M, Wozniak DJ, Stoodley P, Hall-Stoodley L. Prev ention and treatment of Staphylococcus aureus biofilms. Expert Rev Anti-Infect Ther. 2015;13(12):1499–1516. doi: https://doi.org/10.1586/14787210.2015.1100533</mixed-citation><mixed-citation xml:lang="en">Bhattacharya M, Wozniak DJ, Stoodley P, Hall-Stoodley L. Prev ention and treatment of Staphylococcus aureus biofilms. Expert Rev Anti-Infect Ther. 2015;13(12):1499–1516. doi: https://doi.org/10.1586/14787210.2015.1100533</mixed-citation></citation-alternatives></ref><ref id="cit91"><label>91</label><citation-alternatives><mixed-citation xml:lang="ru">Lai Y, Cogen AL, Radek KA, et al. Activation of TLR2 by a small molecule produced by Staphylococcus epidermidis increases antimicrobial defense against bacterial skin infections. J Investig Dermatol. 2010;130(9):2211–2221. doi: https://doi.org/10.1038/jid.2010.123</mixed-citation><mixed-citation xml:lang="en">Lai Y, Cogen AL, Radek KA, et al. Activation of TLR2 by a small molecule produced by Staphylococcus epidermidis increases antimicrobial defense against bacterial skin infections. J Investig Dermatol. 2010;130(9):2211–2221. doi: https://doi.org/10.1038/jid.2010.123</mixed-citation></citation-alternatives></ref><ref id="cit92"><label>92</label><citation-alternatives><mixed-citation xml:lang="ru">Pfalzgra A, Brandenburg K, Weindl G. Antimicrobial Peptides and Their Therapeutic Potential for Bacterial Skin Infections and Wounds. Front Pharmacol. 2018;9:281. doi: https://doi.org/10.3389/fphar.2018.00281</mixed-citation><mixed-citation xml:lang="en">Pfalzgra A, Brandenburg K, Weindl G. Antimicrobial Peptides and Their Therapeutic Potential for Bacterial Skin Infections and Wounds. Front Pharmacol. 2018;9:281. doi: https://doi.org/10.3389/fphar.2018.00281</mixed-citation></citation-alternatives></ref><ref id="cit93"><label>93</label><citation-alternatives><mixed-citation xml:lang="ru">Sørensen OE, Follin P, Johnsen AH, et al. Human cathelicidin, hCAP-18, is processed to the antimicrobial peptide LL-37 by extracellular cleavage with proteinase 3. Blood. 2001;97(12): 3951–3959. doi: https://doi.org/10.1182/blood.v97.12.3951</mixed-citation><mixed-citation xml:lang="en">Sørensen OE, Follin P, Johnsen AH, et al. Human cathelicidin, hCAP-18, is processed to the antimicrobial peptide LL-37 by extracellular cleavage with proteinase 3. Blood. 2001;97(12): 3951–3959. doi: https://doi.org/10.1182/blood.v97.12.3951</mixed-citation></citation-alternatives></ref><ref id="cit94"><label>94</label><citation-alternatives><mixed-citation xml:lang="ru">Murakami M, Ohtake T, Dorschner RA, et al. Cathelicidin antimicrobial peptide expression in sweat, an innate defense system for the skin. J Investig Dermatol. 2002;119(5):1090–1095. doi: https://doi.org/10.1046/j.1523-1747.2002.19507.x</mixed-citation><mixed-citation xml:lang="en">Murakami M, Ohtake T, Dorschner RA, et al. Cathelicidin antimicrobial peptide expression in sweat, an innate defense system for the skin. J Investig Dermatol. 2002;119(5):1090–1095. doi: https://doi.org/10.1046/j.1523-1747.2002.19507.x</mixed-citation></citation-alternatives></ref><ref id="cit95"><label>95</label><citation-alternatives><mixed-citation xml:lang="ru">Yamasaki K, Di Nardo A, Bardan A, et al. Increased serine protease activity and cathelicidin promotes skin inflammation in rosacea. Nat Med. 2007;13(8):975–980. doi: https://doi.org/10.1038/nm1616</mixed-citation><mixed-citation xml:lang="en">Yamasaki K, Di Nardo A, Bardan A, et al. Increased serine protease activity and cathelicidin promotes skin inflammation in rosacea. Nat Med. 2007;13(8):975–980. doi: https://doi.org/10.1038/nm1616</mixed-citation></citation-alternatives></ref><ref id="cit96"><label>96</label><citation-alternatives><mixed-citation xml:lang="ru">Boguniewicz M, Leung DY. Atopic dermatitis: A disease of altered skin barrier and immune dysregulation. Immunol Rev. 2011;242(1):233–246. doi: https://doi.org/10.1111/j.1600065X.2011.01027.x</mixed-citation><mixed-citation xml:lang="en">Boguniewicz M, Leung DY. Atopic dermatitis: A disease of altered skin barrier and immune dysregulation. Immunol Rev. 2011;242(1):233–246. doi: https://doi.org/10.1111/j.1600065X.2011.01027.x</mixed-citation></citation-alternatives></ref><ref id="cit97"><label>97</label><citation-alternatives><mixed-citation xml:lang="ru">Haisma EM, de Breij A, Chan H, et al. LL-37-derived peptides eradicate multidrug-resistant Staphylococcus aureus from thermally wounded human skin equivalents. Antimicrob Agents Chemother. 2014;58(8):4411–4419. doi: https://doi.org/10.1128/AAC.02554-14</mixed-citation><mixed-citation xml:lang="en">Haisma EM, de Breij A, Chan H, et al. LL-37-derived peptides eradicate multidrug-resistant Staphylococcus aureus from thermally wounded human skin equivalents. Antimicrob Agents Chemother. 2014;58(8):4411–4419. doi: https://doi.org/10.1128/AAC.02554-14</mixed-citation></citation-alternatives></ref><ref id="cit98"><label>98</label><citation-alternatives><mixed-citation xml:lang="ru">Mishra B, Golla RM, Lau K, et al. Anti-Staphylococcal Biofilm Effects of Human Cathelicidin Peptides. ACS Med Chem Lett. 2016;7(1):117–121. doi: https://doi.org/10.1021/acsmedchemlett.5b00433</mixed-citation><mixed-citation xml:lang="en">Mishra B, Golla RM, Lau K, et al. Anti-Staphylococcal Biofilm Effects of Human Cathelicidin Peptides. ACS Med Chem Lett. 2016;7(1):117–121. doi: https://doi.org/10.1021/acsmedchemlett.5b00433</mixed-citation></citation-alternatives></ref><ref id="cit99"><label>99</label><citation-alternatives><mixed-citation xml:lang="ru">Biedermann T, Skabytska Y, Kaesler S, Volz T. Regulation of T Cell Immunity in Atopic Dermatitis by Microbes: The Yin and Yang of Cutaneous Inflammation. Front Immunol. 2015;6:353. doi: https://doi.org/10.3389/fimmu.2015.00353</mixed-citation><mixed-citation xml:lang="en">Biedermann T, Skabytska Y, Kaesler S, Volz T. Regulation of T Cell Immunity in Atopic Dermatitis by Microbes: The Yin and Yang of Cutaneous Inflammation. Front Immunol. 2015;6:353. doi: https://doi.org/10.3389/fimmu.2015.00353</mixed-citation></citation-alternatives></ref><ref id="cit100"><label>100</label><citation-alternatives><mixed-citation xml:lang="ru">McLaughlin RA, Hoogewerf AJ. Interleukin-1b-induced growth enhancement of Staphylococcus aureus occurs in biofilm but not planktonic cultures. Microb Pathog. 2006;41(2-3):67–79. doi: https://doi.org/10.1016/j.micpath.2006.04.005</mixed-citation><mixed-citation xml:lang="en">McLaughlin RA, Hoogewerf AJ. Interleukin-1b-induced growth enhancement of Staphylococcus aureus occurs in biofilm but not planktonic cultures. Microb Pathog. 2006;41(2-3):67–79. doi: https://doi.org/10.1016/j.micpath.2006.04.005</mixed-citation></citation-alternatives></ref><ref id="cit101"><label>101</label><citation-alternatives><mixed-citation xml:lang="ru">Lee JH, Del Sorbo L, Khine AA, et al. Modulation of bacterial growth by tumor necrosis factor-alpha in vitro and in vivo. Am J Respir Crit Care Med. 2003;168(12):1462–1470. doi: https://doi.org/10.1164/rccm.200302-303OC</mixed-citation><mixed-citation xml:lang="en">Lee JH, Del Sorbo L, Khine AA, et al. Modulation of bacterial growth by tumor necrosis factor-alpha in vitro and in vivo. Am J Respir Crit Care Med. 2003;168(12):1462–1470. doi: https://doi.org/10.1164/rccm.200302-303OC</mixed-citation></citation-alternatives></ref><ref id="cit102"><label>102</label><citation-alternatives><mixed-citation xml:lang="ru">Hazelbauer GL, Falke JJ, Parkinson JS. Bacterial chemoreceptors: High-performance signaling in networked arrays. Trends Biochem Sci. 2008;33(1):9–19. doi: https://doi.org/10.1016/j.tibs.2007.09.014</mixed-citation><mixed-citation xml:lang="en">Hazelbauer GL, Falke JJ, Parkinson JS. Bacterial chemoreceptors: High-performance signaling in networked arrays. Trends Biochem Sci. 2008;33(1):9–19. doi: https://doi.org/10.1016/j.tibs.2007.09.014</mixed-citation></citation-alternatives></ref><ref id="cit103"><label>103</label><citation-alternatives><mixed-citation xml:lang="ru">Han B, Li M, Xu Y, et al. Tsr Chemoreceptor InteractsWith IL-8 Provoking E. coli Transmigration Across Human Lung Epithel Cells. Sci Rep. 2016;6:31087. doi: https://doi.org/10.1038/srep31087</mixed-citation><mixed-citation xml:lang="en">Han B, Li M, Xu Y, et al. Tsr Chemoreceptor InteractsWith IL-8 Provoking E. coli Transmigration Across Human Lung Epithel Cells. Sci Rep. 2016;6:31087. doi: https://doi.org/10.1038/srep31087</mixed-citation></citation-alternatives></ref><ref id="cit104"><label>104</label><citation-alternatives><mixed-citation xml:lang="ru">Jun SH, Lee JH, Kim SI, et al. Staphylococcus aureus-derived membrane vesicles exacerbate skin inflammation in atopic dermatitis. Clin Exp Allergy. 2017;47:85–96. doi: https://doi.org/10.1111/cea.12851</mixed-citation><mixed-citation xml:lang="en">Jun SH, Lee JH, Kim SI, et al. Staphylococcus aureus-derived membrane vesicles exacerbate skin inflammation in atopic dermatitis. Clin Exp Allergy. 2017;47:85–96. doi: https://doi.org/10.1111/cea.12851</mixed-citation></citation-alternatives></ref><ref id="cit105"><label>105</label><citation-alternatives><mixed-citation xml:lang="ru">Matsuo K, Nagakubo D, Komori Y, et al. CCR4 Is Critically Involved in Skin Allergic Inflammation of BALB/c Mice. J Invest Dermatol. 2018;138(8):1764–1773. doi: https://doi.org/10.1016/j.jid.2018.02.027</mixed-citation><mixed-citation xml:lang="en">Matsuo K, Nagakubo D, Komori Y, et al. CCR4 Is Critically Involved in Skin Allergic Inflammation of BALB/c Mice. J Invest Dermatol. 2018;138(8):1764–1773. doi: https://doi.org/10.1016/j.jid.2018.02.027</mixed-citation></citation-alternatives></ref><ref id="cit106"><label>106</label><citation-alternatives><mixed-citation xml:lang="ru">Yamazaki Y, Nakamura Y, Núñez G. Role of the microbiota in skin immunity and atopic dermatitis. Allergol Int. 2017;66(4): 539–544. doi: https://doi.org/10.1016/j.alit.2017.08.004</mixed-citation><mixed-citation xml:lang="en">Yamazaki Y, Nakamura Y, Núñez G. Role of the microbiota in skin immunity and atopic dermatitis. Allergol Int. 2017;66(4): 539–544. doi: https://doi.org/10.1016/j.alit.2017.08.004</mixed-citation></citation-alternatives></ref><ref id="cit107"><label>107</label><citation-alternatives><mixed-citation xml:lang="ru">Finlay BB, McFadden G. Anti-immunology: Evasion of the host immune system by bacterial and viral pathogens. Cell. 2006;124(4):767–782. doi: https://doi.org/10.1016/j.cell.2006.01.034</mixed-citation><mixed-citation xml:lang="en">Finlay BB, McFadden G. Anti-immunology: Evasion of the host immune system by bacterial and viral pathogens. Cell. 2006;124(4):767–782. doi: https://doi.org/10.1016/j.cell.2006.01.034</mixed-citation></citation-alternatives></ref><ref id="cit108"><label>108</label><citation-alternatives><mixed-citation xml:lang="ru">Gries CM, Kielian T. Staphylococcal Biofilms and Immune Polarization during Prosthetic Joint Infection. J Am Acad Orthop Surg. 2017;25(Suppl 1):20–24. doi: https://doi.org/10.5435/jAAOS-D-16-00636</mixed-citation><mixed-citation xml:lang="en">Gries CM, Kielian T. Staphylococcal Biofilms and Immune Polarization during Prosthetic Joint Infection. J Am Acad Orthop Surg. 2017;25(Suppl 1):20–24. doi: https://doi.org/10.5435/jAAOS-D-16-00636</mixed-citation></citation-alternatives></ref><ref id="cit109"><label>109</label><citation-alternatives><mixed-citation xml:lang="ru">Thurlow LR, Hanke ML, Fritz T, et al. Staphylococcus aureus biofilms prevent macrophage phagocytosis and attenuate inf lamm ation in vivo. J Immunol. 2011;186(11):6585–6596. doi: https://doi.org/10.4049/jimmunol.1002794</mixed-citation><mixed-citation xml:lang="en">Thurlow LR, Hanke ML, Fritz T, et al. Staphylococcus aureus biofilms prevent macrophage phagocytosis and attenuate inf lamm ation in vivo. J Immunol. 2011;186(11):6585–6596. doi: https://doi.org/10.4049/jimmunol.1002794</mixed-citation></citation-alternatives></ref><ref id="cit110"><label>110</label><citation-alternatives><mixed-citation xml:lang="ru">Secor PR, James GA, Fleckman P, et al. Staphylococcus aureus Biofilm and Planktonic cultures differentially impact gene expression, mapk phosphorylation, and cytokine production in human keratinocytes. BMC Microbiol. 2011;11:143. doi: https://doi.org/10.1186/1471-2180-11-143</mixed-citation><mixed-citation xml:lang="en">Secor PR, James GA, Fleckman P, et al. Staphylococcus aureus Biofilm and Planktonic cultures differentially impact gene expression, mapk phosphorylation, and cytokine production in human keratinocytes. BMC Microbiol. 2011;11:143. doi: https://doi.org/10.1186/1471-2180-11-143</mixed-citation></citation-alternatives></ref><ref id="cit111"><label>111</label><citation-alternatives><mixed-citation xml:lang="ru">Hanke ML, Kielian T. Deciphering mechanisms of staphylococcal biofilm evasion of host immunity. Front Cell Infect Microbiol. 2012;2:62. doi: https://doi.org/10.3389/fcimb.2012.00062</mixed-citation><mixed-citation xml:lang="en">Hanke ML, Kielian T. Deciphering mechanisms of staphylococcal biofilm evasion of host immunity. Front Cell Infect Microbiol. 2012;2:62. doi: https://doi.org/10.3389/fcimb.2012.00062</mixed-citation></citation-alternatives></ref><ref id="cit112"><label>112</label><citation-alternatives><mixed-citation xml:lang="ru">Alboslemy T, Yu B, Rogers T, Kim MH. Staphylococcus aureus Biofilm-Conditioned Medium Impairs Macrophage-Mediated Antibiofilm Immune Response by Upregulating KLF2 Expression. Infect Immun. 2019;87(4):e00643-18. doi: https://doi.org/10.1128/IAI.00643-18</mixed-citation><mixed-citation xml:lang="en">Alboslemy T, Yu B, Rogers T, Kim MH. Staphylococcus aureus Biofilm-Conditioned Medium Impairs Macrophage-Mediated Antibiofilm Immune Response by Upregulating KLF2 Expression. Infect Immun. 2019;87(4):e00643-18. doi: https://doi.org/10.1128/IAI.00643-18</mixed-citation></citation-alternatives></ref><ref id="cit113"><label>113</label><citation-alternatives><mixed-citation xml:lang="ru">Hon KL, Tsang YC, Pong NH, et al. Clinical features and Staphylococcus aureus colonization/infection in childhood atopic dermatitis. J Dermatol Treat. 2016;27(3):235–240. doi: https://doi.org/10.3109/09546634.2015.1093586</mixed-citation><mixed-citation xml:lang="en">Hon KL, Tsang YC, Pong NH, et al. Clinical features and Staphylococcus aureus colonization/infection in childhood atopic dermatitis. J Dermatol Treat. 2016;27(3):235–240. doi: https://doi.org/10.3109/09546634.2015.1093586</mixed-citation></citation-alternatives></ref><ref id="cit114"><label>114</label><citation-alternatives><mixed-citation xml:lang="ru">Gonzalez ME, Schaffer JV, Orlow SJ, et al. Cutaneous microbiome effects of fluticasone propionate cream and adjunctive bleach baths in childhood atopic dermatitis. J Am Acad Dermatol. 2016;75(3):481–493. doi: https://doi.org/10.3109/09546634.2015.1093586</mixed-citation><mixed-citation xml:lang="en">Gonzalez ME, Schaffer JV, Orlow SJ, et al. Cutaneous microbiome effects of fluticasone propionate cream and adjunctive bleach baths in childhood atopic dermatitis. J Am Acad Dermatol. 2016;75(3):481–493. doi: https://doi.org/10.3109/09546634.2015.1093586</mixed-citation></citation-alternatives></ref><ref id="cit115"><label>115</label><citation-alternatives><mixed-citation xml:lang="ru">Fukaya M, Sato K, Yamada T, et al. A prospective study of atopic dermatitis managed without topical corticosteroids for a 6-month period. Clin Cosmet Investig Dermatol. 2016;9:151–158. doi: https://doi.org/10.3109/09546634.2015.1093586</mixed-citation><mixed-citation xml:lang="en">Fukaya M, Sato K, Yamada T, et al. A prospective study of atopic dermatitis managed without topical corticosteroids for a 6-month period. Clin Cosmet Investig Dermatol. 2016;9:151–158. doi: https://doi.org/10.3109/09546634.2015.1093586</mixed-citation></citation-alternatives></ref><ref id="cit116"><label>116</label><citation-alternatives><mixed-citation xml:lang="ru">Gong JQ, Lin L, Lin T, et al. Skin colonization by Staphylococcus aureus in patients with eczema and atopic dermatitis and relevant combined topical therapy: A double-blind multicenter randomized controlled trial. Br J Dermatol. 2006;155(4):680–687. doi: https://doi.org/10.1111/j.1365-2133.2006.07410.x</mixed-citation><mixed-citation xml:lang="en">Gong JQ, Lin L, Lin T, et al. Skin colonization by Staphylococcus aureus in patients with eczema and atopic dermatitis and relevant combined topical therapy: A double-blind multicenter randomized controlled trial. Br J Dermatol. 2006;155(4):680–687. doi: https://doi.org/10.1111/j.1365-2133.2006.07410.x</mixed-citation></citation-alternatives></ref><ref id="cit117"><label>117</label><citation-alternatives><mixed-citation xml:lang="ru">Siegfried EC, Jaworski JC, Kaiser JD, Hebert AA. Systematic review of published trials: Long-term safety of topical corticosteroids and topical calcineurin inhibitors in pediatric patients with atopic dermatitis. BMC Pediatr. 2016;16:75. doi: https://doi.org/10.1186/s12887-016-0607-9</mixed-citation><mixed-citation xml:lang="en">Siegfried EC, Jaworski JC, Kaiser JD, Hebert AA. Systematic review of published trials: Long-term safety of topical corticosteroids and topical calcineurin inhibitors in pediatric patients with atopic dermatitis. BMC Pediatr. 2016;16:75. doi: https://doi.org/10.1186/s12887-016-0607-9</mixed-citation></citation-alternatives></ref><ref id="cit118"><label>118</label><citation-alternatives><mixed-citation xml:lang="ru">Yu SH, Drucker AM, Lebwohl M, Silverberg JI. A systematic review of the safety and efficacy of systemic corticosteroids in atopic dermatitis. J Am Acad Dermatol. 2018;78(4):733–740.e1. doi: https://doi.org/10.1016/j.jaad.2017.09.074</mixed-citation><mixed-citation xml:lang="en">Yu SH, Drucker AM, Lebwohl M, Silverberg JI. A systematic review of the safety and efficacy of systemic corticosteroids in atopic dermatitis. J Am Acad Dermatol. 2018;78(4):733–740.e1. doi: https://doi.org/10.1016/j.jaad.2017.09.074</mixed-citation></citation-alternatives></ref><ref id="cit119"><label>119</label><citation-alternatives><mixed-citation xml:lang="ru">Chandra J, Retuerto M, Seité S, et al. Effect of an Emollient on the Mycobiome of Atopic Dermatitis Patients. J Drugs Dermatol. 2018;17(10):1039–1048.</mixed-citation><mixed-citation xml:lang="en">Chandra J, Retuerto M, Seité S, et al. Effect of an Emollient on the Mycobiome of Atopic Dermatitis Patients. J Drugs Dermatol. 2018;17(10):1039–1048.</mixed-citation></citation-alternatives></ref><ref id="cit120"><label>120</label><citation-alternatives><mixed-citation xml:lang="ru">Seite S, Bieber T. Barrier function and microbiotic dysbiosis in atopic dermatitis. Clin Cosmet Investig Dermatol. 2015;8:479–483. doi: https://doi.org/10.2147/CCID.S91521</mixed-citation><mixed-citation xml:lang="en">Seite S, Bieber T. Barrier function and microbiotic dysbiosis in atopic dermatitis. Clin Cosmet Investig Dermatol. 2015;8:479–483. doi: https://doi.org/10.2147/CCID.S91521</mixed-citation></citation-alternatives></ref><ref id="cit121"><label>121</label><citation-alternatives><mixed-citation xml:lang="ru">Bianchi P, Theunis J, Casas C, et al. Effects of a New Emollient-Based Treatment on Skin Microflora Balance and Barrier Function in Children with Mild Atopic Dermatitis. Pediatr Dermatol. 2016;33(2):165–171. doi: https://doi.org/10.1111/pde.12786</mixed-citation><mixed-citation xml:lang="en">Bianchi P, Theunis J, Casas C, et al. Effects of a New Emollient-Based Treatment on Skin Microflora Balance and Barrier Function in Children with Mild Atopic Dermatitis. Pediatr Dermatol. 2016;33(2):165–171. doi: https://doi.org/10.1111/pde.12786</mixed-citation></citation-alternatives></ref><ref id="cit122"><label>122</label><citation-alternatives><mixed-citation xml:lang="ru">Kim JE, Kim HS. Microbiome of the Skin and Gut in Atopic Dermatitis (AD): Understanding the Pathophysiology and Finding Novel Management Strategies. J Clin Med.2019;8(4):444. doi: https://doi.org/10.3390/jcm8040444</mixed-citation><mixed-citation xml:lang="en">Kim JE, Kim HS. Microbiome of the Skin and Gut in Atopic Dermatitis (AD): Understanding the Pathophysiology and Finding Novel Management Strategies. J Clin Med.2019;8(4):444. doi: https://doi.org/10.3390/jcm8040444</mixed-citation></citation-alternatives></ref><ref id="cit123"><label>123</label><citation-alternatives><mixed-citation xml:lang="ru">Chen MH, Chen XJ, Wang M, et al. Ophiopogon japonicus — A phytochemical, ethnomedicinal and pharmacological review. J Ethnopharmacol. 2016;181:193–213. doi: https://doi.org/10.1016/j.jep.2016.01.037</mixed-citation><mixed-citation xml:lang="en">Chen MH, Chen XJ, Wang M, et al. Ophiopogon japonicus — A phytochemical, ethnomedicinal and pharmacological review. J Ethnopharmacol. 2016;181:193–213. doi: https://doi.org/10.1016/j.jep.2016.01.037</mixed-citation></citation-alternatives></ref><ref id="cit124"><label>124</label><citation-alternatives><mixed-citation xml:lang="ru">Lau D, Plotkin BJ. Antimicrobial and Biofilm effects of herbs used in the Traditional Chinese Medicine. Nat Prod Commun. 2013;8(11):1617–1620.</mixed-citation><mixed-citation xml:lang="en">Lau D, Plotkin BJ. Antimicrobial and Biofilm effects of herbs used in the Traditional Chinese Medicine. Nat Prod Commun. 2013;8(11):1617–1620.</mixed-citation></citation-alternatives></ref><ref id="cit125"><label>125</label><citation-alternatives><mixed-citation xml:lang="ru">Gueniche A, Dahel K, Bastien P, et al. Vitreoscilla filiformis bacterial extract to improve the efficacy of emollient used in atopic dermatitis symptoms. J Eur Acad Dermatol Venereol. 2008;22(6): 746–747. doi: https://doi.org/10.1111/j.1468-3083.2007.02428.x</mixed-citation><mixed-citation xml:lang="en">Gueniche A, Dahel K, Bastien P, et al. Vitreoscilla filiformis bacterial extract to improve the efficacy of emollient used in atopic dermatitis symptoms. J Eur Acad Dermatol Venereol. 2008;22(6): 746–747. doi: https://doi.org/10.1111/j.1468-3083.2007.02428.x</mixed-citation></citation-alternatives></ref><ref id="cit126"><label>126</label><citation-alternatives><mixed-citation xml:lang="ru">Gueniche A, Knaudt B, Schuck E, et al. Effects of nonpathogenic gram-negative bacterium Vitreoscilla filiformis lysate on atopic dermatitis: a prospective, randomized, double-blind, placebo-controlled clinical study. Br J Dermatol. 2008;159(6):1357–1363. doi: https://doi.org/10.1111/j.1365-2133.2008.08836.x</mixed-citation><mixed-citation xml:lang="en">Gueniche A, Knaudt B, Schuck E, et al. Effects of nonpathogenic gram-negative bacterium Vitreoscilla filiformis lysate on atopic dermatitis: a prospective, randomized, double-blind, placebo-controlled clinical study. Br J Dermatol. 2008;159(6):1357–1363. doi: https://doi.org/10.1111/j.1365-2133.2008.08836.x</mixed-citation></citation-alternatives></ref><ref id="cit127"><label>127</label><citation-alternatives><mixed-citation xml:lang="ru">Nakatsuii T, Gallo R. Dermatological therapy by topical application of non-pathogenic bacteria. J Invest Dermatol. 2014;134(1): 11–14. doi: https://doi.org/10.1038/jid.2013.379</mixed-citation><mixed-citation xml:lang="en">Nakatsuii T, Gallo R. Dermatological therapy by topical application of non-pathogenic bacteria. J Invest Dermatol. 2014;134(1): 11–14. doi: https://doi.org/10.1038/jid.2013.379</mixed-citation></citation-alternatives></ref><ref id="cit128"><label>128</label><citation-alternatives><mixed-citation xml:lang="ru">Mahe YF, Perez MJ, Tacheau C, et al. New Vitreoscilla filiformis extract grown on spa water-enriched medium activates endogenous cutaneous antioxidant and antimicrobial defenses through a potential Toll-like receptor 2/protein kinase C, zeta transduction pathway. Clin Cosmet Investig Dermatol. 2013;6:191–196. doi: https://doi.org/10.2147/CCID.S47324</mixed-citation><mixed-citation xml:lang="en">Mahe YF, Perez MJ, Tacheau C, et al. New Vitreoscilla filiformis extract grown on spa water-enriched medium activates endogenous cutaneous antioxidant and antimicrobial defenses through a potential Toll-like receptor 2/protein kinase C, zeta transduction pathway. Clin Cosmet Investig Dermatol. 2013;6:191–196. doi: https://doi.org/10.2147/CCID.S47324</mixed-citation></citation-alternatives></ref><ref id="cit129"><label>129</label><citation-alternatives><mixed-citation xml:lang="ru">Seite S, Zelenkova H, Martin R. Clinical efficacy of emollients in atopic dermatitis patients — relationship with the skin microbiota modification. Clin Cosm Invest Dermatol. 2017;10:25–33. doi: https://doi.org/10.2147/CCID.S121910</mixed-citation><mixed-citation xml:lang="en">Seite S, Zelenkova H, Martin R. Clinical efficacy of emollients in atopic dermatitis patients — relationship with the skin microbiota modification. Clin Cosm Invest Dermatol. 2017;10:25–33. doi: https://doi.org/10.2147/CCID.S121910</mixed-citation></citation-alternatives></ref><ref id="cit130"><label>130</label><citation-alternatives><mixed-citation xml:lang="ru">Using a specific emollient to manage skin microbiome dysbiosis. J Am Acad Dermatol. 2016;74(5 Suppl 1):AB89. doi: https://doi.org/10.1016/j.jaad.2016.02.348</mixed-citation><mixed-citation xml:lang="en">Using a specific emollient to manage skin microbiome dysbiosis. J Am Acad Dermatol. 2016;74(5 Suppl 1):AB89. doi: https://doi.org/10.1016/j.jaad.2016.02.348</mixed-citation></citation-alternatives></ref><ref id="cit131"><label>131</label><citation-alternatives><mixed-citation xml:lang="ru">Paufique J. Active ingredient obtained from ophiopogon japonicus for the treatment of atopic dermatitis. U.S. Patent Application No. 16/069,265.</mixed-citation><mixed-citation xml:lang="en">Paufique J. Active ingredient obtained from ophiopogon japonicus for the treatment of atopic dermatitis. U.S. Patent Application No. 16/069,265.</mixed-citation></citation-alternatives></ref><ref id="cit132"><label>132</label><citation-alternatives><mixed-citation xml:lang="ru">Mainzer C, Le Guillou M, Vyumvuhore R, et al. Clinical Efficacy of Oligofructans from Ophiopogon japonicus in Reducing Atopic Dermatitis Flare-ups in Caucasian Patients. Acta Derm Venereol. 2019;99(10):858–864. doi: https://doi.org/10.2340/00015555-3224</mixed-citation><mixed-citation xml:lang="en">Mainzer C, Le Guillou M, Vyumvuhore R, et al. Clinical Efficacy of Oligofructans from Ophiopogon japonicus in Reducing Atopic Dermatitis Flare-ups in Caucasian Patients. Acta Derm Venereol. 2019;99(10):858–864. doi: https://doi.org/10.2340/00015555-3224</mixed-citation></citation-alternatives></ref><ref id="cit133"><label>133</label><citation-alternatives><mixed-citation xml:lang="ru">li Xiong S, Li A, Huang N, et al. Antioxidant and immunoregulatory activity of different polysaccharide fractions from tuber of Ophiopogon japonicus. Carbohydrate Polymers. 2011;86(3): 1273–1280. doi: https://doi.org/10.1016/j.carbpol.2011.06.025</mixed-citation><mixed-citation xml:lang="en">li Xiong S, Li A, Huang N, et al. Antioxidant and immunoregulatory activity of different polysaccharide fractions from tuber of Ophiopogon japonicus. Carbohydrate Polymers. 2011;86(3): 1273–1280. doi: https://doi.org/10.1016/j.carbpol.2011.06.025</mixed-citation></citation-alternatives></ref><ref id="cit134"><label>134</label><citation-alternatives><mixed-citation xml:lang="ru">Response of skin microbiome to emollient treatment in patients with atopic dermatitis. J Am Acad Dermatol. 2016;74 (5 Suppl 1):AB88. doi: https://doi.org/10.1016/j.jaad.2016.02.346</mixed-citation><mixed-citation xml:lang="en">Response of skin microbiome to emollient treatment in patients with atopic dermatitis. J Am Acad Dermatol. 2016;74 (5 Suppl 1):AB88. doi: https://doi.org/10.1016/j.jaad.2016.02.346</mixed-citation></citation-alternatives></ref></ref-list><fn-group><fn fn-type="conflict"><p>The authors declare that there are no conflicts of interest present.</p></fn></fn-group></back></article>
