Kuramitsu Shunichiro, Yamamichi Akane, Ohka Fumiharu, Motomura Kazuya, Hara Masahito, Natsume Atsushi
Department of Neurosurgery, Nagoya University School of Medicine, 65 Tsurumai, Showa-ku, Nagoya 466-8550, Japan.
Immunotherapy. 2016 Dec;8(12):1393-1404. doi: 10.2217/imt-2016-0076.
Patients with glioblastoma have a very poor prognosis. Adoptive cellular therapy (ACT) is defined as the collection of circulating or tumor-infiltrating lymphocytes, their selection, modification, expansion and activation, and their re-administration to patients in order to induce antitumor activity. Although various ACTs have been attempted, most failed to improve the outcome. Immune checkpoint blockade antibodies and T cell engineering with tumor-specific chimeric antigen receptors suggest the emergence of a new era of immunotherapy. Here, we summarize approaches with ACTs using genetically modified T cells, which have been improved by enhancing their antitumor activity, and discuss strategies to develop these therapies. The mechanisms by which gliomas modulate and evade the immune system are also discussed.
胶质母细胞瘤患者的预后非常差。过继性细胞疗法(ACT)的定义为收集循环淋巴细胞或肿瘤浸润淋巴细胞,对其进行筛选、改造、扩增和激活,然后重新注入患者体内以诱导抗肿瘤活性。尽管已经尝试了各种ACT疗法,但大多数都未能改善治疗结果。免疫检查点阻断抗体和带有肿瘤特异性嵌合抗原受体的T细胞工程技术预示着免疫治疗新时代的到来。在此,我们总结了使用基因改造T细胞的ACT疗法,这些疗法通过增强抗肿瘤活性得到了改进,并讨论了开发这些疗法的策略。我们还讨论了胶质瘤调节和逃避免疫系统的机制。