Immunomodulatory drug therapy for the disease caused by SARS-CoV-2 infection (COVID-19)
- Authors: Karateev D.E.1, Luchikhina E.L.1
-
Affiliations:
- Moscow Regional Research and Clinical Institute (MONIKI)
- Issue: Vol 48 (2020): Supplement 1
- Pages: 51-67
- Section: Journal Articles
- URL: https://almclinmed.ru/jour/article/view/1339
- DOI: https://doi.org/10.18786/2072-0505-2020-48-036
- ID: 1339
Cite item
Full Text
Abstract
This systematic review focuses on the state-of-the-art pharmacotherapy of immune disorders in the novel coronavirus infection (COVID-19), leading to a cytokine storm and uncontrolled inflammatory response that causes severe tissue damage and multiple organ failure. A lot of theoretical, experimental and clinical data support the need for immunomodulatory (immunosuppressive) therapy for this disease. It should be emphasized that all immunomodulatory drugs for COVID-19 are prescribed off label, and the evidence base of the results of randomized trials is just being accumulated. We review the immunomodulatory therapy for COVID-19 with the following agents: glucocorticoids, hydroxychloroquine and chloro-quine, type 1 interferons, interleukin-6 antagonists (tocilizumab, sarilumab, olokizumab), interleukin-1 p inhibitor canakinumab, tumour necrosis factor inhibitors (infliximab), Janus kinase (JAK) inhibitors (tofacitinib, baricitinib, ruxolitinib), as well as drugs with other mechanisms of action (abatacept, nivolumab, tacrolimus, sirolimus, fingolimod, melphalan, cyclosporine, methotrexate). At the moment, the most reasonable is the use of interleukin-6 receptor inhibitors, intermediate and high dose glucocorticoids, and JAK inhibitors. Based on the latest data from clinical studies, especially the "Solidarity” trial, the use of hydroxychloroquine and chloroquine seems to have insufficient evidence. There are significant pathophysiological overlaps in the development of immunopathology in COVID-19 and in rheumatic diseases, and the strategy of early aggressive immunosuppressive therapy proposed by a number of researchers almost completely coincides with the current strategies for rheumatoid arthritis.
Keywords
About the authors
D. E. Karateev
Moscow Regional Research and Clinical Institute (MONIKI)
Author for correspondence.
Email: dekar@inbox.ru
ORCID iD: 0000-0002-2352-4080
Dmitry E. Karateev - MD, PhD, Head of Department of Rheumatology; Professor, Chair of Therapy, Postgraduate Training Faculty.
61/2 Shchepkina ul., Moscow, 129110, Tel.: +7 (495) 631 74 16
РоссияE. L. Luchikhina
Moscow Regional Research and Clinical Institute (MONIKI)
Email: eleluch@yandex.ru
ORCID iD: 0000-0002-6519-1106
Elena L. Luchikhina - MD, PhD, Leading Research Fellow, Department of Rheumatology; Associate Professor, Chair of Therapy, Postgraduate Training Faculty.
61/2 Shchepkina ul., Moscow, 129110
РоссияReferences
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