Drexel University College of Medicine, Philadelphia, PA 19129, USA.
J Hematol Oncol. 2013 Jul 8;6:47. doi: 10.1186/1756-8722-6-47.
Recent years have witnessed much progress in both basic research and clinical trials regarding cancer immunotherapy with chimeric antigen receptor (CAR)-engineered T cells. The unique structure of CAR endows T cell tumor specific cytotoxicity and resistance to immunosuppressive microenvironment in cancers, which helps patients to better tackle the issue of immunological tolerance. Adoptive immunotherapy (AIT) using this supernatural T cell have gained momentum after decades of intense debates because of the promising results obtained from preclinical models and clinical trials. However, it is very important for us to evaluate thoroughly the challenges/obstacles before widespread clinical application, which clearly warrants more studies to improve our understanding of the mechanism underlying AIT. In this review, we focus on the critical issues related to the clinical outcomes of CAR-based adoptive immunotherapy and discuss the rationales to refine this new cancer therapeutic modality.
近年来,嵌合抗原受体(CAR)修饰 T 细胞的癌症免疫疗法在基础研究和临床试验方面都取得了很大进展。CAR 的独特结构赋予了 T 细胞对肿瘤的特异性细胞毒性和对癌症中免疫抑制微环境的抗性,这有助于患者更好地解决免疫耐受问题。经过几十年的激烈争论,采用这种超自然 T 细胞的过继免疫疗法(AIT)因临床前模型和临床试验取得的有希望的结果而受到关注。然而,在广泛的临床应用之前,我们非常有必要全面评估挑战/障碍,这显然需要更多的研究来加深我们对 AIT 机制的理解。在这篇综述中,我们重点讨论了与基于 CAR 的过继免疫疗法的临床结果相关的关键问题,并讨论了完善这种新的癌症治疗模式的基本原理。