» Articles » PMID: 38426103

From Neglect to Spotlight: the Underappreciated Role of B Cells in Cutaneous Inflammatory Diseases

Overview
Journal Front Immunol
Date 2024 Mar 1
PMID 38426103
Authors
Affiliations
Soon will be listed here.
Abstract

The skin, covering our entire body as its largest organ, manifests enormous complexities and a profound interplay of systemic and local responses. In this heterogeneous domain, B cells were considered strangers. Yet, recent studies have highlighted their existence in the skin and their distinct role in modulating cutaneous immunity across various immune contexts. Accumulating evidence is progressively shedding light on the significance of B cells in maintaining skin health and in skin disorders. Herein, we integrate current insights on the systemic and local contributions of B cells in three prevalent inflammatory skin conditions: Pemphigus Vulgaris (PV), Systemic Lupus Erythematosus (SLE), and Atopic Dermatitis (AD), underscoring the previously underappreciated importance of B cells within skin immunity. Moreover, we address the potential adverse effects of current treatments used for skin diseases, emphasizing their unintentional consequences on B cells. These comprehensive approaches may pave the way for innovative therapeutic strategies that effectively address the intricate nature of skin disorders.

Citing Articles

IgG from Dermatophagoides pteronyssinus (Der p)-atopic individuals modulates non-atopic thymic B cell phenotype (alfa-4/beta-7) and cytokine production (IFN-γ, IL-9, and IL-10) with direct membrane interaction.

de-Apoena Reche D, Machado N, Fagundes B, Bergamasco I, de Sousa T, do Nascimento L Sci Rep. 2024; 14(1):7274.

PMID: 38538762 PMC: 10973508. DOI: 10.1038/s41598-024-57950-x.

References
1.
Fetter T, Niebel D, Braegelmann C, Wenzel J . Skin-Associated B Cells in the Pathogenesis of Cutaneous Autoimmune Diseases-Implications for Therapeutic Approaches. Cells. 2020; 9(12). PMC: 7762338. DOI: 10.3390/cells9122627. View

2.
Pignarre A, Chatonnet F, Caron G, Haas M, Desmots F, Fest T . Plasmablasts derive from CD23- activated B cells after the extinction of IL-4/STAT6 signaling and IRF4 induction. Blood. 2020; 137(9):1166-1180. DOI: 10.1182/blood.2020005083. View

3.
Kunkel E, Butcher E . Plasma-cell homing. Nat Rev Immunol. 2003; 3(10):822-9. DOI: 10.1038/nri1203. View

4.
Oh J, Iijima N, Song E, Lu P, Klein J, Jiang R . Migrant memory B cells secrete luminal antibody in the vagina. Nature. 2019; 571(7763):122-126. PMC: 6609483. DOI: 10.1038/s41586-019-1285-1. View

5.
Massone C, Kodama K, Salmhofer W, Abe R, Shimizu H, Parodi A . Lupus erythematosus panniculitis (lupus profundus): clinical, histopathological, and molecular analysis of nine cases. J Cutan Pathol. 2005; 32(6):396-404. DOI: 10.1111/j.0303-6987.2005.00351.x. View