生发中心
细胞生物学
CD40
体细胞突变
滤泡树突状细胞
生物
抗原
抗原提呈细胞
B细胞
T细胞
免疫学
抗体
细胞毒性T细胞
免疫系统
遗传学
体外
作者
Julia Merkenschlager,Shlomo Finkin,Víctor Ramos,Julian Kraft,Melissa Cipolla,Carla R. Nowosad,Harald Hartweger,Wenzhu Zhang,Paul Dominic B. Olinares,Anna Gazumyan,Thiago Y. Oliveira,Brian T. Chait,Michel C. Nussenzweig
出处
期刊:Nature
[Nature Portfolio]
日期:2021-02-03
卷期号:591 (7850): 458-463
被引量:113
标识
DOI:10.1038/s41586-021-03187-x
摘要
The germinal centre is a dynamic microenvironment in which B cells that express high-affinity antibody variants produced by somatic hypermutation are selected for clonal expansion by limiting the numbers of T follicular helper cells1,2. Although much is known about the mechanisms that control the selection of B cells in the germinal centre, far less is understood about the clonal behaviour of the T follicular helper cells that help to regulate this process. Here we report on the dynamic behaviour of T follicular helper cell clones during the germinal centre reaction. We find that, similar to germinal centre B cells, T follicular helper cells undergo antigen-dependent selection throughout the germinal centre reaction that results in differential proliferative expansion and contraction. Increasing the amount of antigen presented in the germinal centre leads to increased division of T follicular helper cells. Competition between T follicular helper cell clones is mediated by the affinity of T cell receptors for peptide-major-histocompatibility-complex ligands. T cells that preferentially expand in the germinal centre show increased expression of genes downstream of the T cell receptor, such as those required for metabolic reprogramming, cell division and cytokine production. These dynamic changes lead to marked remodelling of the functional T follicular helper cell repertoire during the germinal centre reaction.
科研通智能强力驱动
Strongly Powered by AbleSci AI