Department of Hematology, Transplantation and Internal Medicine, Medical University of Warsaw, 02-091 Warsaw, Poland.
Department of Biochemistry and Pharmacogenomics, Faculty of Pharmacy, Medical University of Warsaw, 02-091 Warsaw, Poland.
Int J Mol Sci. 2022 Nov 30;23(23):15006. doi: 10.3390/ijms232315006.
Genetically engineered T and NK cells expressing a chimeric antigen receptor (CAR) are promising cytotoxic cells for the treatment of hematological malignancies and solid tumors. Despite the successful therapies using CAR-T cells, they have some disadvantages, such as cytokine release syndrome (CRS), neurotoxicity, or graft-versus-host-disease (GVHD). CAR-NK cells have lack or minimal cytokine release syndrome and neurotoxicity, but also multiple mechanisms of cytotoxic activity. NK cells are suitable for developing an "off the shelf" therapeutic product that causes little or no graft versus host disease (GvHD), but they are more sensitive to apoptosis and have low levels of gene expression compared to CAR-T cells. To avoid these adverse effects, further developments need to be considered to enhance the effectiveness of adoptive cellular immunotherapy. A promising approach to enhance the effectiveness of adoptive cellular immunotherapy is overcoming terminal differentiation or senescence and exhaustion of T cells. In this case, EVs derived from immune cells in combination therapy with drugs may be considered in the treatment of cancer patients, especially effector T and NK cells-derived exosomes with the cytotoxic activity of their original cells.
基因工程表达嵌合抗原受体 (CAR) 的 T 和 NK 细胞是治疗血液系统恶性肿瘤和实体瘤的有前途的细胞毒性细胞。尽管使用 CAR-T 细胞进行了成功的治疗,但它们也存在一些缺点,例如细胞因子释放综合征 (CRS)、神经毒性或移植物抗宿主病 (GVHD)。CAR-NK 细胞缺乏或极少发生细胞因子释放综合征和神经毒性,但也具有多种细胞毒性作用机制。NK 细胞适合开发“现成”的治疗产品,几乎不会或不会引起移植物抗宿主病 (GvHD),但与 CAR-T 细胞相比,它们对细胞凋亡更敏感,基因表达水平更低。为了避免这些不良反应,需要进一步考虑开发,以提高过继细胞免疫疗法的有效性。增强过继细胞免疫疗法的有效性的一种有前途的方法是克服 T 细胞的终末分化或衰老和耗竭。在这种情况下,与药物联合治疗的免疫细胞衍生的 EV 可能被认为是癌症患者的治疗方法,特别是具有其原始细胞细胞毒性作用的效应 T 和 NK 细胞衍生的外泌体。