Borrello Ivan, Noonan Kimberly A
Department of Oncology, Johns Hopkins University , Baltimore, MD , USA.
Front Immunol. 2016 Mar 30;7:112. doi: 10.3389/fimmu.2016.00112. eCollection 2016.
The past several years have witnessed the acceptance of immunotherapy into the mainstream of therapies for patients with cancer. This has been driven by the clinical successes of antibodies to the checkpoint inhibitors, CTLA-4 and PD-1, capable of imparting long-term remissions in several solid tumors as well as Hodgkin's lymphoma (1) and the therapeutic successes of adoptive T-cell transfer with chimeric antigen receptors (2) or modified T-cell receptors (3) that have mostly utilized peripheral T-cells. One emerging area of therapeutic T cell intervention has been the utilization of marrow-infiltrating lymphocytes (MILs) - a novel form of adoptive T-cell therapy. This approach was initially developed to increase the likelihood of a precursor T-cell population with an enhanced tumor specificity in bone marrow (BM)-derived malignancies. However, the unique attributes of BM T-cells and their interaction with their microenvironment provide significant rationale to utilize these cells therapeutically in diseases that extend beyond hematologic malignancies.
在过去几年中,免疫疗法已被纳入癌症患者的主流治疗方法。这是由针对检查点抑制剂CTLA-4和PD-1的抗体在临床上取得的成功所推动的,这些抗体能够使多种实体瘤以及霍奇金淋巴瘤实现长期缓解(1),以及嵌合抗原受体(2)或主要利用外周T细胞的修饰T细胞受体进行过继性T细胞转移的治疗成功(3)。治疗性T细胞干预的一个新兴领域是利用骨髓浸润淋巴细胞(MIL)——一种新型的过继性T细胞疗法。这种方法最初是为了提高在骨髓(BM)来源的恶性肿瘤中具有增强肿瘤特异性的前体T细胞群体的可能性而开发的。然而,BM T细胞的独特特性及其与微环境的相互作用为在血液系统恶性肿瘤以外的疾病中治疗性利用这些细胞提供了重要的理论依据。