Molecular and Systems Pharmacology Graduate Program, Graduate Division of Biological and Biomedical Sciences, Laney Graduate School, Emory University School of Medicine, Atlanta, GA, USA.
Cell and Gene Therapy Program, Department of Pediatrics, Aflac Cancer and Blood Disorders Center, Children's Healthcare of Atlanta and Emory University School of Medicine, Atlanta, GA, USA.
J Hematol Oncol. 2019 Dec 29;12(1):141. doi: 10.1186/s13045-019-0801-y.
Chimeric antigen receptor (CAR) T cell therapy has been successful in treating B cell malignancies in clinical trials; however, fewer studies have evaluated CAR T cell therapy for the treatment of T cell malignancies. There are many challenges in translating this therapy for T cell disease, including fratricide, T cell aplasia, and product contamination. To the best of our knowledge, no tumor-specific antigen has been identified with universal expression on cancerous T cells, hindering CAR T cell therapy for these malignancies. Numerous approaches have been assessed to address each of these challenges, such as (i) disrupting target antigen expression on CAR-modified T cells, (ii) targeting antigens with limited expression on T cells, and (iii) using third party donor cells that are either non-alloreactive or have been genome edited at the T cell receptor α constant (TRAC) locus. In this review, we discuss CAR approaches that have been explored both in preclinical and clinical studies targeting T cell antigens, as well as examine other potential strategies that can be used to successfully translate this therapy for T cell disease.
嵌合抗原受体 (CAR) T 细胞疗法在临床试验中已成功用于治疗 B 细胞恶性肿瘤;然而,较少的研究评估了 CAR T 细胞疗法治疗 T 细胞恶性肿瘤。将这种疗法转化为 T 细胞疾病存在许多挑战,包括同种细胞杀伤、T 细胞发育不全和产品污染。据我们所知,尚未发现在癌细胞上普遍表达的肿瘤特异性抗原,这阻碍了 CAR T 细胞疗法治疗这些恶性肿瘤。已经评估了许多方法来解决这些挑战,例如:(i) 破坏 CAR 修饰的 T 细胞上靶抗原的表达,(ii) 靶向在 T 细胞上表达有限的抗原,以及 (iii) 使用非同种异体反应或已在 T 细胞受体 α 恒定 (TRAC) 基因座进行基因组编辑的第三方供体细胞。在这篇综述中,我们讨论了针对 T 细胞抗原的临床前和临床研究中探索的 CAR 方法,并研究了其他可用于成功将该疗法转化为 T 细胞疾病的潜在策略。