决定异体 CAR T 细胞排斥与扩增的细胞和分子机制
Cellular and molecular mechanisms determining allogeneic CAR T cell rejection and expansion.
我们评估了11例接受单一批次cemacabtagene ansegedleucel(cema-cel)治疗的大B细胞淋巴瘤患者,cemacabtagene ansegedleucel是一种异体抗CD19 CAR T产品。
英文原题:CAR-NK cell therapy for hematologic malignancies: advances, challenges and optimization strategies.
这些进展共同凸显了 CAR-NK 细胞疗法巨大的转化潜力,其良好的安全性特征和在治疗血液恶性肿瘤方面令人鼓舞的抗肿瘤活性进一步强化了这一平台。
CAR-T(CAR-T)细胞疗法在血液系统恶性肿瘤中疗效显著,但其临床应用受细胞因子释放综合征、免疫效应细胞相关神经毒性综合征及移植物抗宿主病等毒性限制。自然杀伤(NK)细胞是先天免疫系统的重要组成部分,无需预先进行抗原致敏即可直接识别并清除肿瘤细胞。利用其固有的异体相容性及现货型应用潜力,嵌合抗原受体 NK(CAR-NK)细胞疗法已成为 CAR-T 的一种有前景的替代方案。尽管 CAR-NK 细胞对血液系统肿瘤具有强效抗肿瘤活性,仍面临多项挑战:CAR 设计需要优化、体内持续性和扩增有限、免疫抑制性肿瘤微环境会抑制功能,以及抗原逃逸、同类相残、宿主免疫排斥和规模化生产等问题。本综述系统总结 CAR-NK 细胞治疗血液系统恶性肿瘤的最新进展,并概述提高疗效的策略,包括新型 CAR 设计、改善持续性和扩增、调节免疫抑制性肿瘤微环境及联合治疗。本文还讨论既往综述较少涉及的抗原逃逸、同类相残和宿主排斥防治,并考察细胞来源与生产流程的优化,特别关注受到较少讨论的新兴细胞分选和冷冻保存平台。此外,本文综述 CAR-NK 的当前临床格局及优化临床应用的潜在策略。总体而言,这些进展凸显 CAR-NK 细胞疗法的显著转化潜力,其良好安全性和令人鼓舞的抗肿瘤活性为治疗血液系统恶性肿瘤提供了支持。
Chimeric antigen receptor T (CAR-T) cell therapy has demonstrated remarkable efficacy in hematologic malignancies; however, its clinical application is limited by toxicities, such as cytokine release syndrome, immune effector cell-associated neurotoxicity syndrome, and graft-versus-host disease. Natural killer (NK) cells, as key components of the innate immune system, can directly recognize and eliminate tumor cells without prior antigen sensitization. Capitalizing on their inherent allogeneic compatibility and potential for off-the-shelf use, chimeric antigen receptor NK (CAR-NK) cell therapy has emerged as a promising alternative to CAR-T strategies. Despite their potent antitumor activity in hematologic cancers, CAR-NK cells face several challenges: the need for optimized CAR designs, limited in vivo persistence and expansion, functional suppression by the immunosuppressive tumor microenvironment, as well as issues of antigen evasion, fratricide, host immune rejection, and scalable manufacturing. This review systematically summarizes recent advances in CAR-NK cell therapy for hematologic malignancies and outlines strategies to enhance its efficacy. These strategies include novel CAR designs, improved persistence and expansion, modulation of the immunosuppressive tumor microenvironment, and synergistic combination therapies. We also address the prevention of antigen evasion, fratricide, and host rejection topics less comprehensively covered in prior reviews. Additionally, we examine the optimization of cell sources and manufacturing processes, with particular emphasis on emerging platforms for cell sorting and cryopreservation that have received limited attention. Furthermore, we discuss the current clinical landscape of CAR-NK cells and potential future strategies for optimizing clinical application. Together, these advances highlight the significant translational potential of CAR-NK cell therapy, a platform strengthened by its favorable safety profile and encouraging antitumor activity for treating hematologic malignancies.
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