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驱动B细胞中T-bet表达的信号。

Signals that drive T-bet expression in B cells.

作者信息

Myles Arpita, Gearhart Patricia J, Cancro Michael P

机构信息

Institute for Immunology, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA 19104, United States.

Laboratory of Molecular Biology and Immunology, National Institute on Aging, National Institutes of Health, Baltimore, MD 21224, United States.

出版信息

Cell Immunol. 2017 Nov;321:3-7. doi: 10.1016/j.cellimm.2017.09.004. Epub 2017 Sep 11.

Abstract

Transcription factors regulate various developmental and functional aspects of B cells. T-bet is a recently appreciated transcription factor associated with "Age-associated B cells" or ABCs, the development of autoimmunity, and viral infections. T-bet expression is favored by nucleic acid-containing antigens and immune complexes and is regulated by interplay between various cytokines, notably, the TFH cytokines IL-21, IL-4 and IFNγ. Adaptive signals by themselves cannot upregulate T-bet; however, they have a synergistic effect on induction of T-bet by innate receptors. The functional role of T-bet+ B cells is unclear, although it is known that T-bet promotes class switching to IgG2a/c. It is likely T-bet serves dichotomous roles in B cells, promoting pathogenic autoreactive antibodies on one hand but mediating microbial immunity on the other, making it a target of interest in both therapeutic and prophylactic settings.

摘要

转录因子调节B细胞的各种发育和功能方面。T-bet是一种最近被认识到的与“年龄相关B细胞”(ABCs)、自身免疫发展和病毒感染相关的转录因子。含核酸抗原和免疫复合物有利于T-bet表达,并且它受多种细胞因子之间相互作用的调节,特别是滤泡辅助性T细胞(TFH)细胞因子白细胞介素-21(IL-21)、白细胞介素-4(IL-4)和干扰素γ(IFNγ)。适应性信号自身不能上调T-bet;然而,它们对先天受体诱导T-bet具有协同作用。尽管已知T-bet促进向IgG2a/c的类别转换,但T-bet阳性B细胞的功能作用尚不清楚。T-bet可能在B细胞中发挥双重作用,一方面促进致病性自身反应性抗体产生,另一方面介导微生物免疫,这使其成为治疗和预防领域中一个值得关注的靶点。

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