细胞毒性T细胞
白细胞介素21
自然杀伤性T细胞
白细胞介素12
细胞生物学
淋巴因子激活杀伤细胞
抗原提呈细胞
白细胞介素2受体
CD8型
生物
NK-92
效应器
T细胞
免疫学
免疫系统
体外
生物化学
作者
Ferdynand J. Kos,Edgar G. Engleman
出处
期刊:Journal of Immunology
[The American Association of Immunologists]
日期:1995-07-15
卷期号:155 (2): 578-584
被引量:84
标识
DOI:10.4049/jimmunol.155.2.578
摘要
Cell-mediated immunity involves the participation of both regulatory and cytotoxic cells. The conversion of precursors to effector CD8+ cytotoxic T (Tc) cells requires cell-cell collaboration in which CD4+ T cells are traditionally viewed as helper cells. An in vitro system was used here to demonstrate that the generation of human alloantigen-specific CD8+ Tc cells requires the participation of CD3-CD16+CD56+ NK cells but not CD4+ T helper cells. Depletion of NK cells from responders abolished the induction of alloantigen-specific Tc cells in mixed lymphocyte cultures (MLC). Purified CD5+CD8+ T cells stimulated with alloantigen proliferated but did not differentiate into fully functional effector Tc cells. Coculture of responder CD5+CD8+ T cells with NK cells promoted the conversion of CD8+ Tc cell precursors (pTc) into effector Tc cells. Anti-CD56 mAbs blocked Tc cell induction in MLC, suggesting a role for CD56 molecules expressed on NK cells in either alloantigen recognition or delivery of accessory signals to pTc cells. These findings suggest a novel critical link between the natural and specific immune responses.
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