细胞毒性T细胞
CD8型
生物
细胞因子
白细胞介素21
干扰素γ
免疫学
分子生物学
免疫系统
生物化学
体外
作者
Subash Sad,Rita Marcotte,Timothy R. Mosmann
出处
期刊:Immunity
[Elsevier]
日期:1995-03-01
卷期号:2 (3): 271-279
被引量:682
标识
DOI:10.1016/1074-7613(95)90051-9
摘要
Alloantigen-stimulated CD8+ mouse spleen cells, either spontaneously or in the presence of IL-12 or IFN gamma plus anti-IL-4, differentiate into CD8+ T cells secreting a Th1-like cytokine pattern (IL-2 and IFN gamma). IL-4 induced differentiation into CD8+ T cells secreting Th2 cytokines (IL-4, IL-5, IL-6, and IL-10), whereas anti-IFN gamma suppressed the development of CD8+ cells secreting IFN gamma. Clones of IL-4- or IFN gamma-producing CD8+ T cells were relatively stable, as IL-4 or IFN gamma did not cause interconversion of committed CD8+ T cells. Both CD8+ subsets were cytotoxic, failed to provide cognate help for B cell antibody production, and remained CD4-, CD8 alpha+ CD8 beta+. We propose the names TC1 and TC2 for cytotoxic CD8+ T cells secreting Th1-like and Th2-like cytokines, respectively.
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