细胞毒性T细胞
生物
癌症
免疫疗法
免疫学
过继性细胞移植
免疫系统
淋巴细胞亚群
癌症免疫疗法
T细胞
癌症研究
谱系(遗传)
癌细胞
Jurkat细胞
免疫检查点
抗原呈递
T淋巴细胞
过继免疫治疗
CD8型
细胞生物学
淋巴细胞活化
自我容忍
作者
Georgia Stevens,Rafael Blanco-Domínguez,Sofia Mensurado,Bruno Silva‐Santos
标识
DOI:10.1146/annurev-immunol-083024-024653
摘要
The success of cancer immunotherapy depends on the mobilization of leukocytes with the capacity to eliminate tumor cells. γδ T cells represent a lymphocyte lineage with strong cytotoxic potential and abundant production of antitumor cytokines. Importantly, they are not restricted to MHC-mediated presentation of neoantigens and thus are highly suited to tackle major challenges in current immunotherapies. In this article, we review the main approaches to engage and expand γδ T cells endogenously (in patients) or exogenously (for adoptive cell therapy) against cancer. We discuss the dichotomy between activation and exhaustion of γδ T cells and how they may benefit from immune checkpoint blockade. Finally, we describe the biological properties of the two main subsets of human γδ T cells, Vδ1 and Vδ2 T cells, and how they are boosted, through genetic engineering, toward maximization of their performance as next-generation cancer immunotherapies.
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