表型
人口
生物
CD28
细胞毒性T细胞
免疫学
T细胞
白细胞介素21
炎症
T淋巴细胞
白细胞介素3
细胞生物学
分子生物学
体外
抗原
免疫系统
遗传学
医学
基因
环境卫生
作者
Akihisa Kawajiri,Jing Li,Keita Koinuma,Ziying Yang,Hye Jin Yoon,Jaeu Yi,Hiroyuki Nagashima,Minami Ishii,Feng Gao,Kosuke Sato,Shunichi Tayama,Hideo Harigae,Yoichiro Iwakura,Naoto Ishii,Alan Sher,Kazuyoshi Ishigaki,Jinfang Zhu,Kwang Soon Kim,Takeshi Kawabe
出处
期刊:Science Advances
[American Association for the Advancement of Science]
日期:2024-12-04
卷期号:10 (49)
被引量:1
标识
DOI:10.1126/sciadv.adq6618
摘要
Memory-phenotype (MP) CD4 + T lymphocytes develop from naïve cells via self-recognition at homeostasis. While previous studies defined MP cells as a heterogeneous population that comprises T helper 1 (T H 1)/17–like subsets, functional significance of the T-bet − Rorγt − subpopulation remains unknown. Here we show that MP lymphocytes as a whole population can differentiate into T H 1/17/regulatory T (T reg ) cells to mediate mild and persistent inflammation in lymphopenic environments, whereas naïve cells exhibit strong, T H 1-dominated responses. Moreover, we demonstrate that MP lymphocytes comprise not only T H 1/17-differentiated subsets but a polyclonal, transcriptomically immature “undifferentiated” subpopulation at homeostasis. Furthermore, our data argue that while the T-bet + Rorγt − MP subset is terminally T H 1-differentiated, its undifferentiated counterpart retains the capacity to rapidly proliferate to differentiate into T H 1/17/T reg cells, with the latter response tonically constrained by preexisting T reg cells. Together, our results identify undifferentiated MP CD4 + T lymphocytes as a unique precursor that has a diverse differentiation potential to generate T H 1/17/T reg cells to contribute to pathogenesis of inflammation.
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