溶瘤病毒
癌症研究
肿瘤细胞
抗原
免疫疗法
癌症
嵌合抗原受体
医学
免疫学
实体瘤
肿瘤微环境
免疫系统
内科学
作者
Xin‐Ying Tang,Yushi Ding,Tao Zhou,Xu Wang,Yong Yang
出处
期刊:Cancer Letters
[Elsevier BV]
日期:2021-01-19
卷期号:503: 69-74
被引量:21
标识
DOI:10.1016/j.canlet.2021.01.014
摘要
Chimeric antigen receptor (CAR) T cell therapy is one of the most promising immunotherapies in the past decade. It brings hope for cure to patients with previously refractory hematological malignancies. However, when translating this strategy into non-hematologic malignancies, the antitumor activity from multiple clinical studies seemed to be subtle or transient. The less satisfying efficacy in solid tumors might at least due to antigen heterogeneity, suboptimal CAR-T cell trafficking and tumor immunosuppressive environment. Here, we will review the updating strategies to challenge the therapeutic impediments of CAR-T therapy in non-hematologic malignancies. We mainly focus on the combination with oncolytic viruses (OV), the born allies for CAR-T cells. In addition to previously reported OVs-arming strategy, we discuss recently proposed tumor-tagging concept by OVs as CAR-T targets, as well as the possible improvements. Overall, tumor-tagging strategy by OVs combination with CAR-T would be a novel and promising solution for the heterogeneity and immunosuppressive microenvironment of solid tumors.
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