Curio Sophie, Jonsson Gustav, Marinović Sonja
Department of Life Sciences, Imperial College London, London, UK.
The University of Queensland Diamantina Institute, The University of Queensland, Woolloongabba, QLD 4102, Australia.
Immunother Adv. 2021 Aug 13;1(1):ltab018. doi: 10.1093/immadv/ltab018. eCollection 2021 Jan.
Cancer immunotherapies have significantly improved patient survival and treatment options in recent years. Nonetheless, the success of immunotherapy is limited to certain cancer types and specific subgroups of patients, making the development of new therapeutic approaches a topic of ongoing research. Chimeric antigen receptor (CAR) cells are engineered immune cells that are programmed to specifically eliminate cancer cells. Ideally, a CAR recognizes antigens that are restricted to tumor cells to avoid off-target effects. NKG2D is an activating immunoreceptor and an important player in anti-tumor immunity due to its ability to recognize tumor cells and initiate an anti-tumor immune response. Ligands for NKG2D are expressed on malignant or stressed cells and typically absent from healthy tissue, making it a promising CAR candidate. Here, we provide a summary of past and ongoing NKG2D-based CAR clinical trials and comment on potential pitfalls.
近年来,癌症免疫疗法显著提高了患者的生存率并增加了治疗选择。尽管如此,免疫疗法的成功仅限于某些癌症类型和特定患者亚组,这使得开发新的治疗方法成为一个持续研究的课题。嵌合抗原受体(CAR)细胞是经过工程改造的免疫细胞,被编程为特异性消除癌细胞。理想情况下,CAR识别仅限于肿瘤细胞的抗原以避免脱靶效应。NKG2D是一种激活型免疫受体,由于其能够识别肿瘤细胞并启动抗肿瘤免疫反应,因此是抗肿瘤免疫中的重要参与者。NKG2D的配体在恶性或应激细胞上表达,而在健康组织中通常不存在,这使其成为一种有前景的CAR候选物。在此,我们总结了过去和正在进行的基于NKG2D的CAR临床试验,并对潜在的陷阱进行评论。
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