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Immunization With a Pneumococcal Polysaccharide Vaccine in Children With Juvenile Idiopathic Arthritis Without Systemic Manifestations: a Prospective Study

https://doi.org/10.15690/vsp.v16i6.1822

Abstract

Background. Patients with juvenile idiopathic arthritis (JIA) have an increased risk of being infected. Approximately half of all serious infections in children with JIA are associated with airway involvement.

Objective. Our aim was to study the efficacy and safety of the pneumococcal 13-valent conjugate vaccine (PCV) in children with JIA.

Methods. In a prospective cohort study, 5 groups were formed:  children with JIA in the remission phase on methotrexate therapy  (group 1) or etanercept (group 2), with JIA in the active phase prior  to the appointment of methotrexate (group 3) or etanercept (group  4), control group (conditionally healthy children). 0.5 ml of the 13-valent PCV was administered once subcutaneously during therapy in patients in the remission phase or 3 weeks before the appointment  of methotrexate or etanercept in patients in the active phase. The  main study outcome was the proportion of patients with a protective  ( 40 mg/L) level of specific anti-pneumococcal antibodies (anti-SPP) IgG to Streptococcus pneumoniae 4 weeks after vaccination. In  addition, we assessed the incidence of infectious events before and  after vaccination as well as changes in the content of a high-sensitivity C-reactive protein, S100 protein, and post-vaccination period.

Results. The study included 125 children. Four weeks after  vaccination, the protective level of anti-SPP IgG was established in  21 (84%) patients in the 1st, 23 (92%) in the 2nd, 22 (88%) in the  3rd, 24 (96%) in the 4th and 5th groups (p =1.0). Increase in the  concentration of S100 protein and high-sensitivity C-reactive protein  after vaccination was not noted. JIA exacerbation episodes were not  recorded in any patient. After immunization, the total number of infectious events decreased in all observed groups (p 0.001). Serious adverse events were not registered during the study.

Conclusion. Vaccination with the 13-valent PCV in children with JIA  is highly effective and is not accompanied by the development of serious adverse events.

About the Authors

Ekaterina I. Alexeeva
National Medical Research Center for Children’s Health Sechenov First Moscow State Medical University (Sechenov University)
Russian Federation

Disclosure of interest:

receiving research grants from pharmaceutical companies  Roche, Pfizer, Centocor, Novartis



Tatiana M. Dvoryakovskaya
National Medical Research Center for Children’s Health Sechenov First Moscow State Medical University (Sechenov University)
Russian Federation

Disclosure of interest:

receiving research grants from pharmaceutical companies Roche, Pfizer



Rina V. Denisova
National Medical Research Center for Children’s Health
Russian Federation

Disclosure of interest:

receiving research grants from pharmaceutical companies Roche, Centocor, Novartis



Ksenia B. Isaeva
National Medical Research Center for Children’s Health
Russian Federation


Margarita A. Soloshenko
National Medical Research Center for Children’s Health
Russian Federation


Anna V. Mamutova
National Medical Research Center for Children’s Health
Russian Federation


Nikolay A. Mayansky
National Medical Research Center for Children’s Health
Russian Federation


Natalia E. Tkachenko
National Medical Research Center for Children’s Health
Russian Federation


Irina V. Zubkova
National Medical Research Center for Children’s Health
Russian Federation


Tatiana A. Kaluzhnaya
National Medical Research Center for Children’s Health
Russian Federation


Firuza Ch. Shakhtakhtinskaya
National Medical Research Center for Children’s Health
Russian Federation


Anna G. Gayvoronskaya
National Medical Research Center for Children’s Health
Russian Federation


Marika I. Broeva
National Medical Research Center for Children’s Health
Russian Federation


Marina V. Fedoseenko
National Medical Research Center for Children’s Health
Russian Federation


References

1. Scott DL, Wolfe F, Huizinga TW. Rheumatoid arthritis. Lancet. 2010;376(9746):1094–1108. doi: 10.1016/s0140-6736(10)60826-4.

2. Young A, Koduri G, Batley M, et al. Mortality in rheumatoid arthritis. Increased in the early course of disease, in ischaemic heart disease and in pulmonary fibrosis. Rheumatology (Oxford). 2007;46(2):350–357. doi: 10.1093/rheumatology/kel253.

3. Doran MF, Crowson CS, Pond GR, et al. Frequency of infection in patients with rheumatoid arthritis compared with controls: a population-based study. Arthritis Rheum. 2002;46(9): 2287–2293. doi: 10.1002/art.10524.

4. Smitten AL, Choi HK, Hochberg MC, et al. The risk of hospitalized infection in patients with rheumatoid arthritis. J Rheumatol. 2008;35(3):387–393. doi: 10.1002/art.23112.

5. Franklin J, Lunt M, Bunn D, et al. Risk and predictors of infection leading to hospitalisation in a large primary-care-derived cohort of patients with inflammatory polyarthritis. Ann Rheum Dis. 2007;66(3):308–312. doi: 10.1136/ard.2006.057265.

6. Starkebaum G. Chronic neutropenia associated with autoimmune disease. Semin Hematol. 2002;39(2):121–127. doi: 10.1053/shem.2002.31918.

7. Wagner UG, Koetz K, Weyand CM, Goronzy JJ. Perturbation of the T cell repertoire in rheumatoid arthritis. Proc Natl Acad Sci U S A. 1998;95(24):14447–14452. doi: 10.1073/pnas.95.24.14447.

8. Koetz K, Bryl E, Spickschen K, et al. T cell homeostasis in patients with rheumatoid arthritis. Proc Natl Acad Sci U S A. 2000;97(16):9203–9208. doi: 10.1073/pnas.97.16.9203.

9. Elkayam O, Caspi D, Reitblatt T, et al. The effect of tumor necrosis factor blockade on the response to pneumococcal vaccination in patients with rheumatoid arthritis and ankylosing spondylitis. Semin Arthritis Rheum. 2004;33(4):283–288. doi: 10.1053/j.semarthrit.2003.10.003.

10. Ruderman EM. Overview of safety of non-biologic and biologic DMARDs. Rheumatology (Oxford). 2012;51 Suppl 6:vi37–43. doi: 10.1093/rheumatology/kes283.

11. Dixon WG, Watson K, Lunt M, et al. Rates of serious infection, including site-specific and bacterial intracellular infection, in rheumatoid arthritis patients receiving anti-tumor necrosis factor therapy: results from the British Society for Rheumatology Biologics Register. Arthritis Rheum. 2006;54(8):2368–2376. doi: 10.1002/art.21978.

12. Thomas E, Symmons DP, Brewster DH, et al. National study of cause-specific mortality in rheumatoid arthritis, juvenile chronic arthritis, and other rheumatic conditions: a 20 year followup study. J Rheumatol. 2003;30(5):958–965.

13. Lim WS, Macfarlane JT, Boswell TC, et al. Study of community acquired pneumonia aetiology (SCAPA) in adults admitted to hospital: implications for management guidelines. Thorax. 2001;56(4):296–301. doi: 10.1136/thorax.56.4.296.

14. Bewick T, Sheppard C, Greenwood S, et al. Serotype prevalence in adults hospitalised with pneumococcal non-invasive communityacquired pneumonia. Thorax. 2012;67(6):540– 545. doi: 10.1136/thoraxjnl-2011-201092.

15. O’Brien KL, Wolfson LJ, Watt JP, et al. Burden of disease caused by Streptococcus pneumoniae in children younger than 5 years: global estimates. Lancet. 2009;374(9693):893–902. doi: 10.1016/S0140-6736(09)61204-6.

16. Hausdorff WP, Bryant J, Paradiso PR, Siber GR. Which pneumococcal serogroups cause the most invasive disease: Implications for conjugate vaccine formulation and use, part I. Clin Infect Dis. 2000;30(1):100–121. doi: 10.1086/313608.

17. Desai SP, Turchin A, Szent-Gyorgyi LE, et al. Routinely measuring and reporting pneumococcal vaccination among immunosuppressed rheumatology outpatients: the first step in improving quality. Rheumatology (Oxford). 2011;50(2):366–372. doi: 10.1093/rheumatology/keq297.

18. Gluck T, Muller-Ladner U. Vaccination in patients with chronic rheumatic or autoimmune diseases. Clin Infect Dis. 2008;46(9):1459–1465. doi: 10.1086/587063.

19. Rahier JF, Moutschen M, Van Gompel A, et al. Vaccinations in patients with immune- mediated inflammatory diseases. Rheumatology (Oxford). 2010;49(10):1815–1827. doi: 10.1093/rheumatology/keq183.

20. Cassidy JT, Petty RE, Laxer RM, Lindsley CB. Textbook of pediatric rheumatology. 6th ed. Philadelphia: Saunders Elsevier; 2011.

21. Kapetanovic MC, Saxne T, Sjoholm A, et al. Influence of methotrexate, TNF blockers and prednisolone on antibody responses to pneumococcal polysaccharide vaccine in patients with rheumatoid arthritis. Rheumatology (Oxford). 2006;45(1):106–111. doi: 10.1093/rheumatology/kei193.

22. Nagel J, Geborek P, Saxne T, et al. The risk of pneumococcal infections after immunization with pneumococcal conjugate vaccine compared to non-vaccinated inflammatory arthritis patients. Scand J Rheumatol. 2015;44(4):271–279. doi: 10.3109/03009742.2014.984754.

23. Алексеева Е.И., Солошенко М.А., Дворяковская Т.М., и др. Эффективность и безопасность иммунизации пневмококковой полисахаридной вакциной детей с ювенильным идиопатическим артритом: предварительные результаты проспективного открытого исследования // Вопросы современной педиатрии. — 2017. — Т. 16. — № 2 — С. 142–147. [Alexeeva EI, Soloshenko MA, Dvoryakovskaya TM, et al. Efficacy and safety of immunization with pneumococcal polysaccharide vaccine in children with juvenile idiopathic arthritis: preliminary results of a prospective open-label study. Current pediatrics. 2017;16(2):142–147. (In Russ).] doi: 10.15690/vsp.v16i2.1715.

24. Коровкина Т.И. Клинико-иммунологическая характеристика и особенности течения поствакцинального периода у детей с ревматическими заболеваниями, привитых против пневмококковой и гриппозной инфекций: Автореф. дис. … канд. мед. наук. — Н. Новгород; 2005. — 26 с. [Korovkina TI. Kliniko-immunologicheskaya kharakteristika i osobennosti techeniya postvaktsinal’nogo perioda u detei s revmaticheskimi zabolevaniyami, privitykh protiv pnevmokokkovoi i grippoznoi infektsii. [dissertation abstract] N. Novgorod; 2005. 26 p. (In Russ).]

25. Приложение к набору Buhlmann MRP8/14 ELISA (Buhlmann Laboratories AG, Швейцария). [Annex to the Buhlmann MRP8 / 14 kit ELISA (Buhlmann Laboratories AG, Switzerland). (In Russ).]

26. Maglione MA, Das L, Raaen L, et al. Safety of vaccines used for routine immunization of U.S. children: a systematic review. Pediatrics. 2014;134(2):325–337. doi: 10.1542/peds.2014-1079.

27. Heijstek MW, de Bruin LMO, Bijl M, et al. EULAR recommendations for vaccination in paediatric patients with rheumatic diseases. Ann Rheum Dis. 2011;70(10):1704–1712. doi: 10.1136/ard.2011.150193.


Review

For citations:


Alexeeva E.I., Dvoryakovskaya T.M., Denisova R.V., Isaeva K.B., Soloshenko M.A., Mamutova A.V., Mayansky N.A., Tkachenko N.E., Zubkova I.V., Kaluzhnaya T.A., Shakhtakhtinskaya F.Ch., Gayvoronskaya A.G., Broeva M.I., Fedoseenko M.V. Immunization With a Pneumococcal Polysaccharide Vaccine in Children With Juvenile Idiopathic Arthritis Without Systemic Manifestations: a Prospective Study. Current Pediatrics. 2017;16(6):493-501. https://doi.org/10.15690/vsp.v16i6.1822

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