中文摘要
嵌合抗原受体(CAR)工程化T(CAR-T)细胞疗法已成为癌症治疗的一种革命性方法,尤其是对血液系统恶性肿瘤。然而,CAR-T 疗法存在一些局限性,包括细胞因子释放综合征(CRS)、免疫细胞相关神经毒性综合征(ICANS),以及由于移植物抗宿主病(GvHD)而难以靶向实体瘤和递送异体细胞疗法。因此,探索其他用于CAR工程的细胞来源非常重要。恒定自然杀伤T(iNKT)细胞是一个潜在的靶点,因为它们具有强大的抗肿瘤能力,且不识别错配的主要组织相容性复合体(MHC)和蛋白质抗原,从而避免了GvHD风险。CAR工程化iNKT(CAR-iNKT)细胞疗法通过克服CAR-T 细胞疗法的缺点同时保留强大的抗肿瘤能力,为癌症免疫治疗提供了一种有前景的新方法。本综述总结了当前的CAR-iNKT细胞产品、其功能和表型,以及它们在现货型癌症免疫治疗中的潜力。
展开英文摘要原文
Chimeric antigen receptor (CAR)-engineered T (CAR-T) cell therapy has emerged as a revolutionary approach for cancer treatment, especially for hematologic cancers.
However, CAR-T therapy has some limitations, including cytokine release syndrome (CRS), immune cellassociated neurologic syndrome (ICANS), and difficulty in targeting solid tumors and delivering allogeneic cell therapy due to graft- versus -host disease (GvHD).
Therefore, it is important to explore other cell sources for CAR engineering. Invariant natural killer T (iNKT) cells are a potential target, as they possess powerful antitumor ability and do not recognize mismatched major histocompatibility complexes (MHCs) and protein antigens, thus avoiding the risk of GvHD.
CAR-engineered iNKT (CAR-iNKT) cell therapy offers a promising new approach to cancer immunotherapy by overcoming the drawbacks of CAR-T cell therapy while retaining potent antitumor capabilities. This review summarizes the current CAR-iNKT cell products, their functions and phenotypes, and their potential for off-the-shelf cancer immunotherapy.
论文信息
- 作者
- Wang Y、Li YR
- 第一作者单位
- Department of Chemistry, Biochemistry, University of Washington, Seattle, WA 98105, USA.United States
- 通讯作者单位
- Department of Microbiology, Immunology and Molecular Genetics, University of California, Los Angeles, Los Angeles, CA 90095, USA.United States
- 文献类型
- 综述
- 期刊
- Current pharmaceutical biotechnology2024