Pemphigoid diseases in patients with end-stage kidney diseases: pathogenesis and treatment.

Front Immunol

Department of Dermatology, State Key Laboratory of Complex Severe and Rare Diseases, National Clinical Research Center for Dermatologic and Immunologic Diseases, Peking Union Medical College Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, China.

Published: July 2024

AI Article Synopsis

  • - Pemphigoid diseases are autoimmune disorders causing blistering, and their connection with end-stage kidney disease (ESKD) needs more research for effective management.
  • - A systematic review found 53 case reports and 8 studies discussing triggers for pemphigoid in ESKD patients, like treatment materials and immune issues, and listed various treatment options.
  • - The best management strategy is to eliminate triggers, although corticosteroids are commonly used despite their limited effectiveness, while other treatments like MMF and rituximab show potential benefits that require more research.

Article Abstract

Background: Pemphigoid diseases constitute a group of autoimmune blistering disorders characterized by subepithelial blistering. The association between pemphigoid diseases and both end-stage kidney disease (ESKD) and its treatment is notable. However, there is limited evidence about the management of pemphigoid diseases in patients with ESKD. This systematic review compiled case reports and relevant studies, summarized the underlying mechanisms of pemphigoid diseases in patients with ESKD, and summarized the efficacy of various therapies.

Methods: A systematic search of PubMed and Embase was performed for articles published between 1982 to June 2, 2024.

Results: Fifty-three case reports and eight relevant studies were included. Triggers for pemphigoids in patients with ESKD included materials used to treat ESKD, immune dysregulation of patients with ESKD, and rejection of renal allograft. Treatment for these patients included removing triggers, as well as administering of corticosteroids, mycophenolate mofetil (MMF), tetracyclines, rituximab, methotrexate, dapsone, azathioprine, cyclosporine, intravenous immunoglobin (IVIG), plasmapheresis, and Janus kinase inhibitors.

Conclusion: Removing triggers is the most effective strategy. Despite their suboptimal efficacy, corticosteroids remain the most commonly used agents in this patient population. MMF, tetracyclines, and rituximab are less used but with benefits. There are significant adverse effects associated with methotrexate treatment. Other treatment may also be beneficial and require further investigation. These findings may enable clinicians to optimize the therapeutic approach for these patients.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC11266006PMC
http://dx.doi.org/10.3389/fimmu.2024.1427943DOI Listing

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