Knox James J, Kaplan David E, Betts Michael R
Department of Microbiology, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA, USA.
Medicine and Research Services, Corporal Michael J. Crescenz VA Medical Center, Philadelphia, PA, USA; Division of Gastroenterology, Department of Medicine, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA, USA.
Cell Immunol. 2017 Nov;321:26-34. doi: 10.1016/j.cellimm.2017.04.012. Epub 2017 Jul 11.
T-bet-expressing B cells, first identified as perpetuators of autoimmunity, were recently shown to be critical for murine antiviral responses. While their role in human viral infections remains unclear, B cells expressing T-bet or demonstrating a related phenotype have been described in individuals chronically infected with HIV or HCV, suggesting these cells represent a component of human antiviral responses. In this review, we discuss the induction of T-bet in B cells following both HIV and HCV infections, the factors driving T-bet B cell expansions, T-bet's relationship to atypical memory B cells, and the consequences of T-bet induction. We propose potential antiviral roles for T-bet B cells and discuss whether this population poses any utility to the HIV and HCV immune responses.
表达T-bet的B细胞最初被鉴定为自身免疫的 perpetuators,最近被证明对小鼠抗病毒反应至关重要。虽然它们在人类病毒感染中的作用尚不清楚,但在慢性感染HIV或HCV的个体中已描述了表达T-bet或表现出相关表型的B细胞,这表明这些细胞是人类抗病毒反应的一个组成部分。在这篇综述中,我们讨论了HIV和HCV感染后B细胞中T-bet的诱导、驱动T-bet B细胞扩增的因素、T-bet与非典型记忆B细胞的关系以及T-bet诱导的后果。我们提出了T-bet B细胞的潜在抗病毒作用,并讨论了这一细胞群体对HIV和HCV免疫反应是否有任何作用。