4.7 Article

Neutrophilic granulocyte-derived B-cell activating factor supports B cells in skin lesions in hidradenitis suppurativa

Journal

JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY
Volume 151, Issue 4, Pages 1015-1026

Publisher

MOSBY-ELSEVIER
DOI: 10.1016/j.jaci.2022.10.034

Keywords

Acne inversa; B cell; Cibersort; G-CSF; granulocyte; IL-17; plasma cell; RNA sequencing; tertiary lymphoid structures; TNF-a; TNFSF13B

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This study aimed to characterize mediators that support B/plasma cell persistence in Hidradenitis suppurativa (HS), a chronic inflammatory disease. The results showed that levels of B/plasma cells, neutrophils, CD81 T cells, and M0 and M1 macrophages were elevated in HS lesions compared to healthy skin. It was found that BAFF, produced by myeloid cells, played a key role in supporting B/plasma cell persistence and function in HS lesions.
Background: Hidradenitis suppurativa (HS) is a chronic inflammatory disease characterized by painful inflamed nodules, abscesses, and pus-draining tunnels appearing in axillary, inguinal, and perianal skin areas. HS lesions contain various types of immigrated immune cells. Objective: This study aimed to characterize mediators that support lesional B/plasma cell persistence in HS. Methods: Skin samples from several cohorts of HS patients and control cohorts were assessed by mRNA sequencing, quantitative PCR on reverse-transcribed RNA, flow cytometry, and immunohistofluorescence. Blood plasma and cultured skin biopsy samples, keratinocytes, dermal fibroblasts, neutrophilic granulocytes (neutrophils), monocytes, and B cells were analyzed. Complex systems biology approaches were used to evaluate bulk and single-cell RNA sequencing data. Results: Proportions of B/plasma cells, neutrophils, CD81 T cells, and M0 and M1 macrophages were elevated in HS lesions compared to skin of healthy and perilesional intertriginous areas. There was an association between B/plasma cells, neutrophils, and B-cell activating factor (BAFF, aka TNFSF13B). BAFF was abundant in HS lesions, particularly in nodules and abscesses. Among the cell types present in HS lesions, myeloid cells were the main BAFF producers. Mechanistically, granulocyte colony-stimulating factor in the presence of bacterial products was the major stimulus for neutrophils' BAFF secretion. Lesional upregulation of BAFF receptors was attributed to B cells (TNFRSF13C/BAFFR and TNFRSF13B/TACI) and plasma cells (TNFRSF17/BCMA). Characterization of the lesional BAFF pathway revealed molecules involved in migration/adhesion (eg, CXCR4, CD37, CD53, SELL), proliferation/survival (eg, BST2), activation (eg, KLF2, PRKCB), and reactive oxygen species production (eg, NCF1, CYBC1) of B/plasma cells. Conclusion: Neutrophil-derived BAFF supports B/plasma cell persistence and function in HS lesions. (J Allergy Clin Immunol 2023;151:1015-26.)

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