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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.v21i5.2458</article-id><article-id custom-type="elpub" pub-id-type="custom">vsp-3039</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>КЛИНИЧЕСКИЕ НАБЛЮДЕНИЯ</subject></subj-group><subj-group subj-group-type="section-heading" xml:lang="en"><subject>CLINICAL OBSERVATIONS</subject></subj-group></article-categories><title-group><article-title>Особенности применения генно-инженерной биологической терапии (устекинумаб) у детей с псориазом при наличии сопутствующего метаболического синдрома или неэффективности предшествующей биологической терапии: клинические наблюдения</article-title><trans-title-group xml:lang="en"><trans-title>Administration Details of Genetically Engineered Biologic Drug (Ustekinumab) in Children with Psoriasis and Comorbid Metabolic Syndrome or in Case of Previous Biological Therapy Failure: Case Studies</trans-title></trans-title-group></title-group><contrib-group><contrib contrib-type="author" corresp="yes"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0002-0081-0981</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>Иванов Роман Александрович - врач отделения дерматологии с группой лазерной хирургии Научно-исследовательского института детской дерматологии НМИЦ здоровья детей.</p><p>119296, Москва, Ломоносовский пр-т, д. 2, стр. 1</p></bio><bio xml:lang="en"><p>Moscow</p></bio><email xlink:type="simple">isxiks@gmail.com</email><xref ref-type="aff" rid="aff-1"/></contrib><contrib contrib-type="author" corresp="yes"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0003-2252-8570</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>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; ЦГМА Управления делами Президента РФ<country>Россия</country></aff><aff xml:lang="en">National Medical Research Center of Children’s Health; 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; 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><pub-date pub-type="collection"><year>2022</year></pub-date><pub-date pub-type="epub"><day>08</day><month>11</month><year>2022</year></pub-date><volume>21</volume><issue>5</issue><fpage>419</fpage><lpage>429</lpage><permissions><copyright-statement>Copyright &amp;#x00A9; Иванов Р.А., Мурашкин Н.Н., 2022</copyright-statement><copyright-year>2022</copyright-year><copyright-holder xml:lang="ru">Иванов Р.А., Мурашкин Н.Н.</copyright-holder><copyright-holder xml:lang="en">Ivanov R.A., Murashkin N.N.</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/3039">https://vsp.spr-journal.ru/jour/article/view/3039</self-uri><abstract><sec><title>Обоснование</title><p>Обоснование. Псориаз — хроническое иммуноопосредованное заболевание многофакторной природы, которое зачастую требует назначения генно-инженерных биологических препаратов. Назначение последних имеет ряд особенностей и рисков, а также зависит от множества факторов. Рассмотрены результаты применения устекинумаба в качестве препарата выбора при наличии сопутствующего метаболического синдрома у ребенка с синдромом Дауна, а также случая неэффективности предшествующей биологической терапии ингибиторами.</p><p>Описание клинических случаев. Представлено описание двух клинических случаев терапии с применением устекинумаба у детей с псориазом тяжелого течения. В первом случае рассмотрена ситуация выбора системной терапии у ребенка, страдающего синдромом Дауна и имеющего сложный коморбидный фон: ожирение и стеатогепатит. Второй случай интересен выбором тактики лечения у пациента с отягощенным по псориазу семейным анамнезом, длительно получающего метотрексат, а затем этанерцепт с последующей потерей эффективности и выраженным обострением заболевания на фоне отсутствия патогенетической терапии.</p></sec><sec><title>Заключение</title><p>Заключение. Исходя из результатов исследований и рассмотренных клинических ситуаций, можно утверждать, что устекинумаб является предпочтительным биологическим препаратом для лечения детей с тяжелым течением псориаза, имеющих коморбидные патологии и нуждающихся в переключении биологического агента в связи с неэффективностью предшествующей терапии.</p></sec></abstract><trans-abstract xml:lang="en"><sec><title>Background</title><p>Background. Psoriasis is a chronic immune-mediated disease with multifactorial nature. It often requires administration of genetically engineered biologic drugs. They have a number of features and risks that depend on various factors. The results of ustekinumab administration as a drug of choice in patients with comorbid metabolic syndrome in a child with Down syndrome, as well as a case of inefficacy of previous biologic therapy with inhibitors are considered.</p><p>Clinical cases description. Two clinical cases of ustekinumab administration in children with severe psoriasis have been described. In the first case, we had to choose systemic therapy for the child suffering from Down syndrome and having complex comorbid background: obesity and steatohepatitis. The second case was interesting due to the family history of psoriasis in the patient, who received methotrexate for a long time, and then etanercept with subsequent loss of efficacy and severe disease aggravation without any pathogenetic therapy.</p></sec><sec><title>Conclusion</title><p>Conclusion. Ustekinumab is the favorable genetically engineered biologic drug (according to the studies results and the clinical cases data) for children with severe psoriasis who have comorbid pathologies and who require the change in biologic agent due to its inefficacy.</p></sec></trans-abstract><kwd-group xml:lang="ru"><kwd>дети</kwd><kwd>псориаз</kwd><kwd>генно-инженерные биологические препараты</kwd><kwd>устекинумаб</kwd><kwd>коморбидность</kwd><kwd>синдром Дауна</kwd><kwd>неалкогольная жировая болезнь печени</kwd><kwd>выживаемость терапии</kwd></kwd-group><kwd-group xml:lang="en"><kwd>children</kwd><kwd>psoriasis</kwd><kwd>genetically engineered biologic drugs</kwd><kwd>ustekinumab</kwd><kwd>comorbidity</kwd><kwd>Down syndrome</kwd><kwd>non-alcoholic fatty liver disease</kwd><kwd>therapy survivability</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">Greb J, Goldminz A, Elder J, et al. 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