Abstract

The pathogenesis of bullous pemphigoid (BP) is characterized by the T cell-dependent production of autoantibodies. Recent studies have indicated that follicular T helper cells (Tfh), the key modulator of B cell activation and autoantibody production, are critical in the development of several autoimmune diseases. Tfh cells perform their functions via IL-21, their hallmark cytokine. In the present study, the frequencies of Tfh cells were investigated in the peripheral blood samples of BP patients to evaluate whether Tfh cells involve in this clinical entity. Significantly higher Tfh cell counts were observed in the peripheral blood of BP patients than those in healthy controls (median: 11.25% vs. 4.95%, respectively; P<0.001). Additionally, the serum IL-21 levels in BP patients were higher than those of the healthy controls (median: 103.98 pg/mL vs 46.77 pg/mL, respectively; P<0.001). The frequencies of Tfh cells and IL-21 levels were both positively correlated with anti-BP180-NC16A autoantibody titers (R = 0.712, P<0.01 and R = 0.578, P = 0.030, respectively). After effective therapy, the frequencies of Tfh cells as well as the serum IL-21 levels in BP patients decreased along with clinical improvement. Most importantly, Tfh depleted CD4+ T cells and anti-IL-21 neutralization antibody could inhibit the T cell-induced B cell activation and secretion of BP autoantibody in vitro. Those results suggest that Tfh cells play an important role in autoantibody production and are involved in the pathogenesis of BP.

Highlights

  • Bullous pemphigoid (BP) is an autoimmune subepidermal blistering disease characterized by production of autoantibody directly responding to hemidesmosomal proteins within the dermal-epidermal junction [1,2,3]

  • CD19+ B cells and CD4+ T cells were isolated from 6 BP patients and 6 sex- and age-matched healthy controls

  • An increase in the Tfh cell counts was observed in the peripheral blood of BP patients as compared with those of healthy controls

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Summary

Introduction

Bullous pemphigoid (BP) is an autoimmune subepidermal blistering disease characterized by production of autoantibody directly responding to hemidesmosomal proteins within the dermal-epidermal junction [1,2,3]. The major function of Tfh cells is to help B cells activation and antibody production during humoral immune responses, via interactions between molecules on the surface of Tfh cells and receptors or ligands located on the surface of B cells [12]. Consist with the location in B cell follicles, Tfh cells express high levels of CXCR5, ICOS, PD-1, CD40 ligand (CD40L), OX40, and SLAMassociated protein (SAP), allowing themselves to migrate to the germinal center (GC) and to activate B cells [13,14]. IL-21 was a cytokine preferentially expressed by Tfh cells and served as an important regulator of humoral responses by directly regulating

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