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:Chimeric antigen receptor T-cell therapy in patients with malignant glioma-From neuroimmunology to clinical trial design considerations.
评估嵌合抗原受体(CAR)T 细胞疗法用于恶性胶质瘤患者的临床试验,在儿童和成人患者中展现出一定的早期希望。
评估嵌合抗原受体(CAR)T细胞疗法治疗恶性胶质瘤患者的临床试验,在儿童和成人患者中均显示出初步疗效。然而,其长期获益和安全性仍有待确立。CAR T细胞疗法最终能否成功治疗恶性胶质瘤,取决于能否深入理解中枢神经系统(CNS)实质的免疫学特征,并制定策略以克服胶质瘤特异性抗原表达稀少且异质性显著的问题。此外,还需应对免疫抑制性的“冷”肿瘤微环境、CAR T细胞耗竭以及局部和全身性免疫抑制。本文讨论CAR T细胞疗法的基础知识与科学考量,并重点介绍近期临床试验。为帮助确定最佳CAR T细胞给药途径,我们总结了当前对CNS免疫学及T细胞向CNS归巢的认识,并讨论临床试验设计以及患者安全性监测方面的挑战与机遇。最后,我们探讨CAR T细胞疗法治疗恶性胶质瘤的前景,重点讨论联合治疗和新型工程化策略,以克服免疫调节机制。我们希望本综述能为多学科协作推动该领域发展奠定基础。
Clinical trials evaluating chimeric antigen receptor (CAR) T-cell therapy in patients with malignant gliomas have shown some early promise in pediatric and adult patients. However, the long-term benefits and safety for patients remain to be established. The ultimate success of CAR T-cell therapy for malignant glioma will require the integration of an in-depth understanding of the immunology of the central nervous system (CNS) parenchyma with strategies to overcome the paucity and heterogeneous expression of glioma-specific antigens. We also need to address the cold (immunosuppressive) microenvironment, exhaustion of the CAR T-cells, as well as local and systemic immunosuppression. Here, we discuss the basics and scientific considerations for CAR T-cell therapies and highlight recent clinical trials. To help identify optimal CAR T-cell administration routes, we summarize our current understanding of CNS immunology and T-cell homing to the CNS. We also discuss challenges and opportunities related to clinical trial design and patient safety/monitoring. Finally, we provide our perspective on future prospects in CAR T-cell therapy for malignant gliomas by discussing combinations and novel engineering strategies to overcome immuno-regulatory mechanisms. We hope this review will serve as a basis for advancing the field in a multiple discipline-based and collaborative manner.
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