scispace - formally typeset
Open AccessJournal ArticleDOI

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

Reads0
Chats0
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, …

read more

Citations
More filters
Book ChapterDOI

Microorganisms in the Pathogenesis and Management of Spondyloarthritis

TL;DR: In this paper , the authors reviewed the available evidence supporting the notion that spondyloarthritis is a microbiome-driven disease and discussed how genetic, environmental, and microbiota-specific interactions may affect the host immune response and lead to inflammation and autoimmunity.
Journal ArticleDOI

Temporal Changes in SARS-CoV-2 Infection Pattern in Patients Admitted with Hematological Diseases—A Single Center Experience from North India

TL;DR: In this paper , the authors compared the outcomes and risk factors for poor survival in patients with hematological conditions hospitalized with COVID-19 infection and found that the delta variant of the virus is associated with higher mortality.
Journal ArticleDOI

Monoclonal anti-CD20 antibodies in lymphomas therapy during the COVID-19 pandemic: pro and contra

TL;DR: In this paper , the authors presented the results of a combined analysis of literature data and own clinical observations regarding the safety and feasibility of using monoclonal anti-CD20 antibodies in the treatment of B-cell lymphoproliferative diseases during the COVID-19 pandemic.
Journal ArticleDOI

Kv1.3 blockade by ShK186 modulates CD4+ effector memory T-cell activity of patients with Granulomatosis with polyangiitis.

TL;DR: In this article , ShK-186 was used to modulate CD4+TEM cell activity via Kv1.3 blockade using the specific peptide inhibiter, Shk-186.
References
More filters
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.
Related Papers (5)