CD19: a promising target for systemic sclerosis.

Front Immunol

Department of Dermatology, Kanazawa Red Cross Hospital, Japanese Red Cross Society, Kanazawa, Ishikawa, Japan.

Published: October 2024

AI Article Synopsis

  • * Therapies that deplete B cells, particularly those targeting CD20 like rituximab, have shown promise in alleviating symptoms such as skin and lung issues in SSc patients.
  • * Newer treatments focusing on CD19, such as Uplizna, may offer greater efficacy and target a wider range of B cells, but ongoing clinical trials are needed to determine their long-term safety and effectiveness for SSc.

Article Abstract

Systemic sclerosis (SSc) is an autoimmune disease characterized by immune dysregulation, vascular damage, and fibrosis. B cells play a significant role in SSc through autoantibody production, cytokine secretion, and T cell regulation. Autoantibodies like anti-topoisomerase I and anti-RNA polymerase III are specific to SSc and linked to clinical features such as skin and lung involvement. B cell depletion therapies, particularly anti-CD20 antibodies like rituximab, have shown benefits in treating SSc, improving skin and lung disease symptoms. However, CD19, another B cell marker, is more widely expressed and has emerged as a promising target in autoimmune diseases. CD19-targeted therapies, such as CAR T cells and Uplizna (inebilizumab), have demonstrated potential in treating refractory autoimmune diseases, including SSc. Uplizna offers advantages over rituximab by targeting a broader range of B cells and showing higher efficacy in specific patient subsets. Clinical trials currently investigate Uplizna's effectiveness in SSc, particularly in severe cases. While these therapies offer hope, long-term safety and efficacy remain unknown. SSc is still a complex disease, but advancing B cell-targeted treatments could significantly improve patient outcomes and knowledge about the pathogenesis.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC11484411PMC
http://dx.doi.org/10.3389/fimmu.2024.1454913DOI Listing

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