Experience with the use of netakimab for the treatment of psoriasis in HIV-infected patients


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Abstract

Background. In HIV-infected patients, psoriasis is classified as a common skin pathology; it often occurs in severe forms in this category of patients. In this regard, the issues of psoriasis therapy, the use of modern methods of treatment remain relevant. Objective. Evaluation of the possibility of using the drug Netakimab in HIV-infected patients. Methods. Five HIV-infected patients with psoriasis vulgaris were followed-up; all patients received antiretroviral therapy (ART). There were 4 men (80%), 1 woman (20%). The mean age in the groups was 36.4 years (from 32 to 41 years). The mean duration of psoriasis was 7.6 years (from 0.5 to 17 years); in one patient, psoriasis developed against the background of HIV infection (3 months after the verification of the HIV diagnosis). PASI was 17.5 (from 14.8 to 35.4). 3 patients had psoriatic arthropathy. The mean duration of HIV infection was 4.5 years (range 0.5 to 9 years), duration of ART was on average 2.5 years (range 0.5 to 7.2 years). All patients underwent the necessary examination before using Netakimab. Results. after 14 weeks of therapy, there was a significant improvement in skin status, a decrease in the inflammatory process in the joints with a complete resolution of the pain syndrome in HIV-infected patients with psoriasis. There was no deterioration in the indicators of HIV infection (clinical course, a decrease in the number of CD4+ lymphocytes, an increase in the HIV viral load). Conclusion. Netakimab in HIV-infected patients can be used to treat severe forms of psoriasis.

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About the authors

Evgeny Yu. Evdokimov

Central Research Institute of Epidemiology

Email: evdokimovevg@yandex.ru
Cand. Sci. (Med.), Researcher at the Clinical Department Moscow, Russia

Zh. B Ponezheva

Central Research Institute of Epidemiology

Moscow, Russia

E. V Svechnikova

Polyclinic № 1 of the Department for Presidential Affairs of the Russian Federation; Novosibirsk State Medical University

Moscow, Russia; Novosibirsk, Russia

B. M Gruzdev

Novosibirsk State Medical University; Infectious Clinical Hospital № 2 of the Moscow Healthcare Department

Novosibirsk, Russia; Moscow, Russia

References

  1. Евдокимов Е.Ю., Сундуков А.В. Псориаз у ВИЧ-инфицированных больных: клинико-лабораторная оценка, подходы к терапии. Российский журнал кожных и венерических болезней. 2017;20(4):227-31. doi: 10.18821/1560-9588-2017-20-4-227-231.
  2. Peter J., Choshi P., Lehloenya R.J. Drug hypersensitivity in HIV infection. Curr Opin Allergy Clin Immunol. 2019;19(4):272-82. doi: 10.1097/ACI.0000000000000545.
  3. Menter A., Strober B.E., Kaplan D.H., et al. Joint AAD-NPF guidelines of care for the management and treatment of psoriasis with biologics. J Am Acad Dermatol. 2019;80(4):1029- 72. doi: 10.1016/j.jaad.2018.11.057.
  4. Евдокимов Е.Ю., Понежева Ж.Б., Свечникова Е.В., Сундуков А.В. Возможности применения антицитокиновых препаратов при воспалительных дерматозах у ВИЧ-позитивных пациентов. Фарматека. 2021;28(10):69-79. doi: 10.18565/pharmateca.2021.10.69-79.
  5. Sellam J., Bouvard B., Masson C., et al. Use of infliximab to treat psoriatic arthritis in HIV-positive patients. Joint Bone Spine. 2007;74(2):197-200. doi: 10.1016/j.jbspin.2006.05.012.
  6. Bartos G., Cline A., Beroukhim K., et al. Current biological therapies for use in HIV-positive patients with psoriasis: case report of gesulkumab used and review. Dermatol Online J. 2018;24(11):19090/qt9db748cg.
  7. Адаскевич В.П. Диагностические индексы в дерматологии. М.,2014. 952 с.
  8. Жукова О.В., Касихина Е.И., Острецова М.Н., Потекаев Н.Н. Новые возможности системной терапии бляшечного псориаза ингибитором ИЛ29P19 рисанкизумабом. Медицинский совет. 2021;8:40-50. doi: 10.21518/2079-701X-2021-8-40-50.
  9. Carlin C.S., Feldman S.R., Krueger J.G., et al. A 50% reduction in the Psoriasis Area and Severity Index (PASI 50) is a clinically significant endpoint in the assessment of psoriasis. J Am Acad Dermatol. 2004;50(6):859-66. doi: 10.1016/j.jaad.2003.09.014.
  10. Common Terminology Criteria for Adverse Events v4.0 (CTCAE). Publish Date: May 28, 2009.
  11. Arican O., Aral M., Sasmaz S., Ciragil P Serum levels of TNF-alpha, -FN-gamm, IL-6, IL-8, IL-12, IL-17, and IL-18 in patients with active psoriasis and correlation with disease severity. Mediators Inflamm. 2005;2005(5):273-79. doi: 10.1155/MI.2005.273

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