» Articles » PMID: 38504438

Beyond the Skin: B Cells in Pemphigus Vulgaris, Tolerance and Treatment

Overview
Journal Br J Dermatol
Specialty Dermatology
Date 2024 Mar 20
PMID 38504438
Authors
Affiliations
Soon will be listed here.
Abstract

Pemphigus vulgaris (PV) is a rare autoimmune bullous disease characterized by blistering of the skin and mucosa owing to the presence of autoantibodies against the desmosome proteins desmoglein 3 and occasionally in conjunction with desmoglein 1. Fundamental research into the pathogenesis of PV has revolutionized its treatment and outcome with rituximab, a B-cell-depleting therapy. The critical contribution of B cells to the pathogenesis of pemphigus is well accepted. However, the exact pathomechanism, mechanisms of onset, disease course and relapse remain unclear. In this narrative review, we provide an overview of the fundamental research progress that has unfolded over the past few centuries to give rise to current and emerging therapies. Furthermore, we summarize the multifaceted roles of B cells in PV, including their development, maturation and antibody activity. Finally, we explored how these various aspects of B-cell function contribute to disease pathogenesis and pave the way for innovative therapeutic interventions.

Citing Articles

The impact of signaling pathways on the desmosome ultrastructure in pemphigus.

Schmitt T, Huber J, Pircher J, Schmidt E, Waschke J Front Immunol. 2025; 15:1497241.

PMID: 39882246 PMC: 11774707. DOI: 10.3389/fimmu.2024.1497241.


IgG reactivity to different desmoglein-3 ectodomains in pemphigus vulgaris: novel panels for assessing disease severity.

Tavakolpour S, Noormohammadi Z, Daneshpazhooh M, Gholami A, Mahmoudi H Front Immunol. 2024; 15:1469937.

PMID: 39416775 PMC: 11479927. DOI: 10.3389/fimmu.2024.1469937.