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Increased risk for severe COVID-19 in patients with inflammatory rheumatic diseases treated with rituximab.

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TLDR
Accumulating data suggest that baseline use of bDMARDs is not associated with worse COVID-19 outcome and that some caution may have to be applied when employing rituximab (RTX), a B-cell depleting b DMARD, in patients with immune-mediated disease.
Abstract
It is currently unknown whether immunosuppressive and/or immunomodulating agents such as biological disease-modifying antirheumatic drugs (bDMARDs) affect the rate and the outcome of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infections of patients with inflammatory rheumatic diseases (IRDs) While several national authorities have defined patients under immunosuppressive therapy as at risk for severe COVID-19,1 accumulating data from individual cases and also from case series, such as a series from Italy published in the Annals of the Rheumatic Diseases by Monti et al 2 and a report about patients with immune-mediated inflammatory diseases from New York,3 suggest that baseline use of bDMARDs is not associated with worse COVID-19 outcome Although the idea of a potentially protective effect of bDMRADs in COVID-19 is intriguing, we feel that extrapolation of these initial data is dangerous and potentially harmful In particular, some caution may have to be applied when employing rituximab (RTX), a B-cell depleting bDMARD, in patients with immune-mediated disease This notion may be illustrated by the following observations: We recently lost two patients with rheumatoid arthritis (RA) treated with RTX to lethal COVID-19 The first patient, a 71-year-old man with rheumatoid factor positive, …

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Journal ArticleDOI

COVID-19 und rheumatische Erkrankungen – bisherige Erkenntnisse der Pandemie

TL;DR: In this paper, ein vergleichbarer Effekt auch unter der Therapie mit Januskinase-Inhibitoren bei Patienten mit rheumatoider Arthritis besteht, wird derzeit untersucht.
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COVID-19 vaccination in individuals with inflammatory rheumatic diseases

TL;DR: In particular, the effects of immunomodulatory therapies on vaccine success are poorly understood as discussed by the authors , and three notable papers from the past year have helped to fill these knowledge gaps.
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COVID-19 course in granulomatosis with polyangiitis: single center experience with review of the literature.

TL;DR: In this paper , the authors conducted a systematic literature review using different spelling combinations of COVID-19 and polyangiitis (GPA) in the PUBMED database.
Journal ArticleDOI

Humoral and cellular immunity in patients with rare autoimmune rheumatic diseases following SARS-CoV-2 vaccination

TL;DR: Following two doses, most RAIRD patients have lower antibody levels than the lowest HC and lower anti-spike T cells, which are associated with reduced immunogenicity compared with a longer pre-vaccination period.
References
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Journal ArticleDOI

Clinical course of COVID-19 in a series of patients with chronic arthritis treated with immunosuppressive targeted therapies.

TL;DR: The survey investigated the patients’ health conditions, the presence of contacts with subjects known to be affected by COVID-19 and management of patients with chronic arthritis treated with biological disease-modifying antirheumatic drugs followed up at the biological outpatient clinic in Pavia, Lombardy.
Journal ArticleDOI

Covid-19 in Immune-Mediated Inflammatory Diseases - Case Series from New York.

TL;DR: Patients in New York City with known immune-mediated inflammatory disease in whom Covid-19 developed while they were receiving treatment with the drug are described.
Journal ArticleDOI

Subcutaneous tanezumab for osteoarthritis of the hip or knee: efficacy and safety results from a 24-week randomised phase III study with a 24-week follow-up period

TL;DR: Tanezumab 5 mg statistically significantly improved pain, physical function and PGA-OA, but tanezumsumab 2.5‬mg only achieved two co-primary end points, but there was a statistically significant improvement in WOMAC Pain and Physical Function, but not PGA -OA.
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