CAR-T therapy for ovarian cancer: Recent advances and future directions

被引:3
|
作者
Xin, Qianling [1 ]
Chen, Yizhao [2 ]
Sun, Xiaojing [1 ]
Li, Ruilin [3 ]
Wu, Yujing [2 ]
Huang, Xuegui [1 ]
机构
[1] Anhui Women & Childrens Med Ctr, Dept Obstet & Gynecol, Hefei 230001, Peoples R China
[2] Anhui Med Univ, Inst Clin Pharmacol, Anhui Collaborat Innovat Ctr Antiinflammatory & Im, Key Lab Antiinflammatory & Immune Med, Hefei, Peoples R China
[3] Anhui Med Univ, Affiliated Hosp 3, Hefei Peoples Hosp 1, Dept Pharm, Hefei, Peoples R China
关键词
Ovarian cancer; Immunotherapy; Chimeric antigen receptor; T cell; NK cell; Macrophage; SOLID TUMORS; CELLS; ANTIGEN; B7-H3; IMMUNOTHERAPY; EXPANSION; RESPONSES; SURVIVAL;
D O I
10.1016/j.bcp.2024.116349
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Ovarian cancer (OC) is a common gynecological tumor with high mortality, which is difficult to control its progression with conventional treatments and is prone to recurrence. Recent studies have identified OC as an immunogenic tumor that can be recognized by the host immune system. Immunotherapy for OC is being evaluated, but approaches such as immune checkpoint inhibitors have limited efficacy, adoptive cell therapy is an alternative therapy, in which CAR(chimeric antigen receptor)-T therapy has been applied to the clinical treatment of hematological malignancies. In addition, CAR-NK and CAR-macrophage (CAR-M) have also shown great potential in the treatment of solid tumors. Here, we discuss recent advances in preclinical and clinical studies of CAR-T for OC treatment, introduce the efforts made by researchers to modify the structure of CAR in order to achieve effective OC immunotherapy, as well as the research status of CAR-NK and CAR-M, and highlight emerging therapeutic opportunities that can be utilized to improve the survival of patients with OC using CARbased adoptive cell therapy.
引用
收藏
页数:10
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