4.4 Review

COVID-19 and the clinical course of rheumatic manifestations

Journal

CLINICAL RHEUMATOLOGY
Volume 40, Issue 7, Pages 2611-2619

Publisher

SPRINGER LONDON LTD
DOI: 10.1007/s10067-021-05691-x

Keywords

Induced autoimmunity; Post-COVID-19; Rheumatic diseases

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COVID-19 can lead to various autoimmune disorders, post-COVID-19 syndromes, and multi-system inflammatory syndrome. The infection of SARS-CoV-2 may cause endotheliitis and thrombosis, activate immune systems, and result in the formation of autoantibodies. It is important to monitor recovery patients for autoimmune manifestations and production of autoantibodies in the context of rheumatic diseases.
The manifestations of COVID-19 have been evolving over time. Various post-COVID-19 syndromes are being recognised. Various viruses have been implicated in the pathogenesis of autoimmune diseases, and we expect a similar outcome with the severe acute respiratory syndrome-associated coronavirus-2 (SARS-CoV-2). The SARS-CoV-2 virus penetrates various tissues and organs and has a predisposition to lead to endotheliitis that may cause vascular manifestations including thrombosis. SARS-CoV-2 has been shown to activate Toll-like receptors and the complement system. It perpetuates NETosis and leads to autoantibody formation. These predispose to systemic autoimmunity. Both reactive arthritis and connective tissue disorders such as lupus and inflammatory myositis have been reported after COVID-19. Other reported autoimmune disorders include haemolytic anaemia, immune thrombocytopenia, cutaneous vasculitis, and Guillain Barre-like acute demyelinating disorders. The multi-system inflammatory syndrome in children and its adult counterpart are another post-COVID-19 entity that presents as an admixture of Kawasaki disease and staphylococcal toxic shock syndrome. Patients with preexisting rheumatic diseases may flare during the SARS-CoV-2 infection. They may develop novel autoimmune features also. The immune-suppressants used during the acute COVID-19 illness may confound the outcomes whereas comorbidities present in patients with rheumatic diseases may mask them. There is an urgent need to follow-up patients recovering from COVID and monitor autoantibody production in the context of rheumatic manifestations.

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