Hoseini Sayed Shahabuddin, Cheung Nai-Kong V
Department of Pediatrics, Memorial Sloan Kettering Cancer Center, United States.
Department of Pediatrics, Memorial Sloan Kettering Cancer Center, United States.
Cancer Lett. 2017 Jul 28;399:44-52. doi: 10.1016/j.canlet.2017.04.013. Epub 2017 Apr 17.
Hepatocellular carcinoma (HCC) is one of the most lethal cancers worldwide with an overall survival rate of less than 15% in developed countries. Despite attempts at new therapeutic strategies, the majority of patients succumb to this cancer. Buttressed by the highly successful clinical impact in melanoma, immunotherapy is gaining momentum as the next treatment modality for many human cancers. Chimeric antigen receptors (CAR) contain the antigen binding moieties of a monoclonal antibody and the co-stimulatory and signaling domains associated with effector receptor signaling. Bispecific antibodies (BsAb) combine the binding specificities of two different monoclonal antibodies, one activating a receptor on a killer effector cell, while the other engaging a tumor-associated antigen to initiate tumor cytotoxicity. In this review, we survey the HCC targets for which CARs and bispecific antibodies have been generated. The pros and cons of these targets for T-cell and Natural Killer cell based immunotherapy will be discussed.
肝细胞癌(HCC)是全球最致命的癌症之一,在发达国家总体生存率低于15%。尽管尝试了新的治疗策略,但大多数患者仍死于这种癌症。受黑色素瘤临床治疗取得巨大成功的推动,免疫疗法作为许多人类癌症的下一种治疗方式正获得越来越多的关注。嵌合抗原受体(CAR)包含单克隆抗体的抗原结合部分以及与效应受体信号传导相关的共刺激和信号传导结构域。双特异性抗体(BsAb)结合了两种不同单克隆抗体的结合特异性,一种激活杀伤效应细胞上的受体,另一种与肿瘤相关抗原结合以启动肿瘤细胞毒性。在本综述中,我们调查了已开发出CAR和双特异性抗体的HCC靶点。将讨论这些靶点在基于T细胞和自然杀伤细胞的免疫疗法中的优缺点。