Instituto de Medicina Molecular, Faculdade de Medicina, Universidade de Lisboa, Lisboa, Portugal.
Cancer Res. 2010 Dec 15;70(24):10024-7. doi: 10.1158/0008-5472.CAN-10-3236.
Abundant interferon-γ secretion, potent cytotoxicity, and major histocompatibility complex-independent targeting of a large spectrum of tumors make γδ T cells attractive mediators of cancer immunotherapy. However, a better understanding of the molecular mechanisms involved in tumor cell recognition and γδ T-cell activation is required to improve the limited success of γδ T-cell-mediated treatments. Here, we review key advances in basic knowledge made over the past 3 years, and summarize the results of γδ T-cell-based clinical trials concluded to date. We also highlight new research directions on the basis of the modulation of receptors that control the function of γδ T cells.
大量的干扰素-γ分泌、强大的细胞毒性以及对多种肿瘤的主要组织相容性复合体非依赖性靶向作用,使 γδ T 细胞成为癌症免疫治疗的有吸引力的介质。然而,为了提高 γδ T 细胞介导的治疗方法的有限成功率,需要更好地了解肿瘤细胞识别和 γδ T 细胞激活中涉及的分子机制。在这里,我们回顾了过去 3 年在基础知识方面取得的重要进展,并总结了迄今为止已完成的基于 γδ T 细胞的临床试验的结果。我们还根据控制 γδ T 细胞功能的受体的调节,强调了新的研究方向。