细胞毒性T细胞
白细胞介素21
抗原提呈细胞
自然杀伤性T细胞
CD8型
生物
CD40
T细胞
体外
细胞生物学
免疫系统
分子生物学
免疫学
化学
生物化学
作者
Benoît P Nicolet,Aurélie Guislain,Monika C. Wolkers
出处
期刊:Journal of Immunology
[The American Association of Immunologists]
日期:2021-12-15
卷期号:207 (12): 2966-2975
被引量:21
标识
DOI:10.4049/jimmunol.2100138
摘要
CD4+ T cells are key contributors in the induction of adaptive immune responses against pathogens. Even though CD4+ T cells are primarily classified as noncytotoxic helper T cells, it has become appreciated that a subset of CD4+ T cells is cytotoxic. However, tools to identify these cytotoxic CD4+ T cells are lacking. We recently showed that CD29 (integrin β1, ITGB1) expression on human CD8+ T cells enriches for the most potent cytotoxic T cells. In this study, we questioned whether CD29 expression also associates with cytotoxic CD4+ T cells. We show that human peripheral blood-derived CD29hiCD4+ T cells display a cytotoxic gene expression profile, which closely resembles that of CD29hi cytotoxic CD8+ T cells. This CD29hi cytotoxic phenotype was observed ex vivo and was maintained in in vitro cultures. CD29 expression enriched for CD4+ T cells, which effectively produced the proinflammatory cytokines IFN-γ, IL-2, and TNF-α, and cytotoxic molecules. Lastly, CD29-expressing CD4+ T cells transduced with a MART1-specific TCR showed target cell killing in vitro. In conclusion, we demonstrate in this study that CD29 can be employed to enrich for cytotoxic human CD4+ T cells.
科研通智能强力驱动
Strongly Powered by AbleSci AI