Novel antigens of CAR T cell therapy: New roads; old destination

被引:27
|
作者
Kozani, Pooria Safarzadeh [1 ]
Kozani, Pouya Safarzadeh [2 ,3 ]
Rahbarizadeh, Fatemeh [1 ,4 ]
机构
[1] Tarbiat Modares Univ, Fac Med Sci, Dept Med Biotechnol, POB 14115-111, Tehran, Iran
[2] Guilan Univ Med Sci, Fac Paramed, Dept Med Biotechnol, Rasht, Iran
[3] Guilan Univ Med Sci, Sch Nursing Midwifery & Paramed, Med Biotechnol Res Ctr, Student Res Comm, Rasht, Iran
[4] Tarbiat Modares Univ, Res & Dev Ctr Biotechnol, Tehran, Iran
来源
TRANSLATIONAL ONCOLOGY | 2021年 / 14卷 / 07期
关键词
Cancer immunotherapy; Adoptive cell therapy; CasMab; Tumor-associated antigens; Chimeric antigen receptor; PHASE-I TRIAL; IMMUNE-RESPONSES; SOLID TUMORS; RECEPTOR; GENE; SAFETY; LYMPHOCYTES; EFFICACY; NANOBODY; SWITCH;
D O I
10.1016/j.tranon.2021.101079
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Chimeric antigen receptor T cell (CAR-T) therapy has so far proved itself as a reliable therapeutic option for the treatment of relapsed/refractory (R/R) B-cell acute lymphoblastic leukemia (B-ALL), diffuse large B-cell lymphoma (DLBCL), multiple myeloma (MM), and mantle cell lymphoma (MCL). However, this picture is not as colorful when it comes to the treatment of solid tumors mainly due to the lack of definitive tumor antigens, as well as the immunosuppressive tumor microenvironments and poor CAR-T infiltration. The recent developments in bioinformatics and cell biology, such as single-cell RNA sequencing, have offered silver linings in the subject of tumor antigen discovery. In the current review, we summarize the development of some CAR-T therapies that target novel tumor antigens, rather than the traditionally CAR-T-targeted ones, and briefly discuss the clinical antitumor achievements of those evaluated in patients, so far. Furthermore, we propose some tumor antigens that might someday be therapeutically beneficial while targeted by CAR-Ts based on the experimental evaluations of their specific monoclonal antibodies.
引用
收藏
页数:12
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