Department of Melanoma Medical Oncology and Department of Immunology, MD Anderson Cancer Center, Houston, TX, USA.
Immunol Rev. 2014 Jan;257(1):250-63. doi: 10.1111/imr.12134.
Adoptive T-cell therapy involves the ex vivo enrichment and expansion of tumor-reactive T cells for infusion. As an immune-based approach, adoptive therapy has become an increasingly attractive modality for the treatment of patients with cancer due to its potential for high specificity, non-cross resistance with conventional therapies, and promise of long-term immunoprotection. In recent years, a resurgence in discoveries underlying T-cell recognition, tumor immune evasion, and T-cell memory and differentiation coupled with the development of several enabling technologies have facilitated a renewed focus in the field of adoptive therapy and its transition to the clinical arena as a treatment modality for patients with cancer. In this review, endogenous T cells derived from peripheral blood or tumor sites will be presented as a source of effector cells for adoptive therapy and strategies to isolate, manipulate, and enhance the function of antigen-specific T cells in vitro and to augment their in vivo efficacy and persistence by host immunomodulation are presented in the context of an ever-increasing inventory of preclinical and clinically available reagents. Optimizing the combination of adoptive cellular therapy and other immune-based and conventional approaches will herald a new generation of research and clinical opportunities for cancer immunotherapy.
过继性 T 细胞疗法包括体外富集和扩增肿瘤反应性 T 细胞以进行输注。作为一种基于免疫的方法,过继性疗法由于其具有高特异性、与常规疗法无交叉耐药性以及长期免疫保护的潜力,已成为治疗癌症患者的一种越来越有吸引力的治疗方式。近年来,T 细胞识别、肿瘤免疫逃逸以及 T 细胞记忆和分化的基础发现出现了复兴,再加上几种使能技术的发展,促使人们重新关注过继性治疗领域,并将其作为癌症患者的一种治疗方式推向临床领域。在本综述中,将外周血或肿瘤部位来源的内源性 T 细胞作为过继性治疗的效应细胞来源,并介绍了在不断增加的临床前和临床可用试剂的背景下,分离、操纵和体外增强抗原特异性 T 细胞功能,以及通过宿主免疫调节增强其体内疗效和持久性的策略。优化过继性细胞治疗与其他基于免疫和常规方法的联合应用,将为癌症免疫治疗带来新一代的研究和临床机会。