SJI 2020 special issue: A catalogue of Ovarian Cancer targets for CAR therapy

被引:9
作者
Benard, Emmanuelle [1 ]
Casey, Nicholas P. [1 ]
Inderberg, Else Marit [1 ]
Walchli, Sebastien [1 ]
机构
[1] Oslo Univ Hosp, Dept Oncol, Translat Res Unit, Sect Cellular Therapy, Oslo, Norway
基金
芬兰科学院;
关键词
CAR T cell; ovarian cancer; tumour microenvironment; CHIMERIC ANTIGEN RECEPTOR; T-CELL THERAPY; 5T4 ONCOFETAL ANTIGEN; ANTITUMOR-ACTIVITY; SOLID TUMORS; PHAGE DISPLAY; TRANSCOELOMIC METASTASIS; PHASE-I; MESOTHELIN; EXPRESSION;
D O I
10.1111/sji.12917
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Ovarian Cancer (OC) is currently difficult to cure, mainly due to its late detection and the advanced state of the disease at the time of diagnosis. Therefore, conventional treatments such as debulking surgery and combination chemotherapy are rarely able to control progression of the tumour, and relapses are frequent. Alternative therapies are currently being evaluated, including immunotherapy and advanced T cell-based therapy. In the present review, we will focus on a description of those Chimeric Antigen Receptors (CARs) that have been validated in the laboratory or are being tested in the clinic. Numerous target antigens have been defined due to the identification of OC biomarkers, and many are being used as CAR targets. We provide an exhaustive list of these constructs and their current status. Despite being innovative and efficient, the OC-specific CARs face a barrier to their clinical efficacy: the tumour microenvironment (TME). Indeed, effector cells expressing CARs have been shown to be severely inhibited, rendering the CAR T cells useless once at the tumour site. Herein, we give a thorough description of the highly immunosuppressive OC TME and present recent studies and innovations that have enabled CAR T cells to counteract this negative environment and to destroy tumours.
引用
收藏
页数:17
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