| Literature DB >> 28833081 |
Guang Yang1, Xiaosu Yang1, Junmei Zhang2, Guancheng Li3, Dandan Zheng1, Anjiao Peng1, Jue Hu4, Liqun Xu1, Baifeng Yang1, Huan Yang1, Wenbin Zhou1, Erdem Tuzun5, Jing Li1.
Abstract
The B-lymphocyte-induced maturation protein 1 (Blimp1) regulates T-cell homeostasis and function. Loss of Blimp1 could double the proportion of follicular regulatory T (Tfr) cells. However, the effects that Blimp1 may have on the function of Tfr cells remain unknown. Here we document the function for Blimp1 in Tfr cells in vitro and in vivo. Data presented in this study demonstrate that Tfr cells indirectly inhibit the activation and differentiation of B cells by negatively regulating follicular helper T cells, so lowering the secretion of antibody. Lack of Blimp1 makes the immune suppression function of Tfr cells impaired in vitro. In the in vivo study, adoptive transfer of Tfr cells could reduce immune responses in germinal centres and relieve the muscle weakness symptoms of mice with experimental autoimmune myasthenia gravis. Blimp1 deficiency resulted in reduced suppressive ability of Tfr cells. This study identifies that Tfr cells are potent suppressors of immunity and are controlled by Blimp1.Entities:
Keywords: T follicular helper cell; autoinflammatory disease; neuroimmunology; neuroinflammation; regulatory T cells
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Year: 2017 PMID: 28833081 PMCID: PMC5721240 DOI: 10.1111/imm.12815
Source DB: PubMed Journal: Immunology ISSN: 0019-2805 Impact factor: 7.397