Dermatology Department, INSERM U976, Rouen University Hospital, Rouen, France.
Dermatology Department, INSERM U976, Saint Louis University Hospital, Paris, France.
Front Immunol. 2018 Apr 13;9:622. doi: 10.3389/fimmu.2018.00622. eCollection 2018.
B cells are major effector cells in autoimmunity through antibody production, T cell help and pro-inflammatory cytokine production. Major advances have been made in human B cell biology knowledge using rituximab and type II new anti-CD20 antibodies, anti-CD19 antibodies, anti-CD22 antibodies, autoantigen specific B cell depleting therapy (chimeric antigen receptor T cells), and B cell receptor signaling inhibition (Bruton's tyrosine kinase inhibitors). However, in certain circumstances B cell depleting therapy may lead to the worsening of the autoimmune disease which is in accordance with the existence of a regulatory B cell population. Current concepts and future directions for B cell modulating therapies in autoimmune diseases with a special focus on pemphigus are discussed.
B 细胞通过产生抗体、辅助 T 细胞和产生促炎细胞因子成为自身免疫中的主要效应细胞。通过利妥昔单抗和新型 II 型抗 CD20 抗体、抗 CD19 抗体、抗 CD22 抗体、自身抗原特异性 B 细胞耗竭疗法(嵌合抗原受体 T 细胞)和 B 细胞受体信号抑制(布鲁顿酪氨酸激酶抑制剂),我们在人类 B 细胞生物学知识方面取得了重大进展。然而,在某些情况下,B 细胞耗竭疗法可能会导致自身免疫性疾病的恶化,这与调节性 B 细胞群体的存在是一致的。本文讨论了自身免疫性疾病中 B 细胞调节治疗的现有概念和未来方向,特别关注天疱疮。