当前基于nkg2d的CAR临床试验综述。

IF 4.1 Q2 IMMUNOLOGY
Immunotherapy advances Pub Date : 2021-08-13 eCollection Date: 2021-01-01 DOI:10.1093/immadv/ltab018
Sophie Curio, Gustav Jonsson, Sonja Marinović
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引用次数: 24

摘要

近年来,癌症免疫疗法显著改善了患者的生存和治疗选择。尽管如此,免疫疗法的成功仅限于某些癌症类型和特定的患者亚组,这使得开发新的治疗方法成为正在进行的研究的主题。嵌合抗原受体(CAR)细胞是经过工程改造的免疫细胞,经过编程可以特异性地消除癌细胞。理想情况下,CAR可以识别局限于肿瘤细胞的抗原,以避免脱靶效应。NKG2D是一种激活性免疫受体,由于其识别肿瘤细胞和启动抗肿瘤免疫应答的能力,在抗肿瘤免疫中发挥重要作用。NKG2D的配体在恶性或应激细胞上表达,通常在健康组织中不存在,使其成为有希望的CAR候选者。在这里,我们总结了过去和正在进行的基于nkg2d的CAR临床试验,并对潜在的缺陷进行了评论。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
A summary of current NKG2D-based CAR clinical trials.

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.

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