Objectives Behçet’s disease (BD) is a systemic vasculitis characterized by recurrent oral and genital ulcers. The disease can manifest diverse phenotypes -such as mucocutaneous, ocular BD- with an uncertain role for autoantibodies in disease pathogenesis. Altered γδT-cell and B-cell phenotypes have been widely reported in BD, but it remains unknown whether these lineages can interact to promote autoantibody production. Methods This study included 75 patients with a BD diagnosis, alongside 41 healthy control (HC) volunteers. We performed ex vivo flow-cytometric profiling of blood γδT and B cells, established a cell culture system to investigate plasma cell generation in vitro , and quantified anti-HSP60 autoantibody levels in BD and HC participants’ serum and cell culture supernatants. Results BD patients with active disease displayed a significant increase in the frequency of cells CXCR5 + PD-1 + Vδ2 T cells resembling a follicular helper-like functional state. Upon stimulation, Vδ2 T cells from BD patients showed increased expression of ICOS and CXCR5, induced significant B cell proliferation, and promoted differentiation of plasma cells in vitro . Cultures of cells from BD patients contained increased levels of multiple cytokines that can support plasma cell differentiation (IL-4, IL-10, IL-17, CXCL13, TNF-α, IFN-γ). Anti-HSP60 autoantibodies were significantly enriched in blood serum from BD patients with active disease as well as the supernatants of patient-derived cell cultures compared to the healthy volunteer cell cultures. Conclusion Our findings suggest that γδT cells may enhance B-cell differentiation into antibody-producing plasma cells in BD patients with mucocutaneous and ocular clinical phenotypes.
Mohammed et al. (Mon,) studied this question.