a Department of Medicine , Royal Marsden Hospital , Sutton , UK.
Expert Rev Hematol. 2016;9(2):123-35. doi: 10.1586/17474086.2016.1122513. Epub 2016 Jan 6.
Checkpoint inhibitors with monoclonal antibodies targeting the CTLA-4 or PD-1 axis have revolutionized treatment in some solid tumors, especially melanoma and lung. The role of the CTLA-4 and PD-1 pathways and their inhibition in lymphoma may be different compared to solid tumors. In heavily pretreated Hodgkin lymphoma, PD-1-directed treatment has led to high remission rates. Several studies are now conducted also including diffuse large B-cell and follicular lymphoma. Besides antibody-based immunotherapy, treatment with chimeric antigen receptor (CAR) T-cells has also come back to the focus of recent studies. Clinical evidence of CAR T-cell treatment in B-cell malignancies is limited to small series, because of the dedicated resources needed. However, impressive response rates have been observed, but toxicities associated with cytokine release can be very severe and fatal. We herein review the background, early clinical evidence, and future perspectives of T-cell-directed immune manipulation for lymphomas including checkpoint inhibitors and CAR T-cell therapies.
针对 CTLA-4 或 PD-1 轴的单克隆抗体检查点抑制剂已经彻底改变了某些实体瘤(尤其是黑色素瘤和肺癌)的治疗方法。与实体瘤相比,CTLA-4 和 PD-1 通路及其抑制在淋巴瘤中的作用可能有所不同。在经过大量预处理的霍奇金淋巴瘤中,PD-1 靶向治疗导致了高缓解率。目前正在进行几项研究,也包括弥漫性大 B 细胞淋巴瘤和滤泡性淋巴瘤。除了抗体免疫疗法外,嵌合抗原受体 (CAR) T 细胞的治疗也重新成为最近研究的焦点。CAR T 细胞治疗 B 细胞恶性肿瘤的临床证据仅限于小系列,因为需要专门的资源。然而,已经观察到令人印象深刻的缓解率,但与细胞因子释放相关的毒性可能非常严重和致命。我们在此回顾了针对淋巴瘤的 T 细胞定向免疫治疗的背景、早期临床证据和未来前景,包括检查点抑制剂和 CAR T 细胞疗法。