Antigen-presenting cells as specialized drivers of intestinal T cell functions

被引:4
|
作者
Kedmi, Ranit [1 ]
Littman, Dan R. [2 ,3 ,4 ]
机构
[1] Weizmann Inst Sci, Dept Syst Immunol, IL-76100 Rehovot, Israel
[2] NYU Grossman Sch Med, Dept Cell Biol, New York, NY 10016 USA
[3] NYU Langone Hlth, Perlmutter Canc Ctr, New York, NY 10016 USA
[4] Howard Hughes Med Inst, New York, NY 10016 USA
关键词
CLASSICAL DENDRITIC CELLS; MHC CLASS-II; GUT MICROBIOTA; REG-CELLS; DIFFERENTIATION; TH17; HOMEOSTASIS; INDUCTION; TOLERANCE; BACTERIA;
D O I
10.1016/j.immuni.2024.09.011
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
The immune system recognizes a multitude of innocuous antigens from food and intestinal commensal microbes toward which it orchestrates appropriate, non-inflammatory responses. This process requires antigen-presenting cells (APCs) that induce T cells with either regulatory or effector functions. Compromised APC function disrupts the T cell balance, leading to inflammation and dysbiosis. Although their precise identities continue to be debated, it has become clear that multiple APC lineages direct the differentiation of distinct microbiota-specific CD4+ T cell programs. Here, we review how unique APC subsets instruct T cell differentiation and function in response to microbiota and dietary antigens. These discoveries provide new opportunities to investigate T cell-APC regulatory networks controlling immune homeostasis and perturbations associated with inflammatory and allergic diseases.
引用
收藏
页码:2269 / 2279
页数:11
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