Antigen-Specific TCR-T Cells for Acute Myeloid Leukemia: State of the Art and Challenges

被引:17
作者
Kang, Synat [1 ]
Li, Yisheng [2 ]
Qiao, Jingqiao [2 ]
Meng, Xiangyu [2 ]
He, Ziqian [2 ]
Gao, Xuefeng [1 ,2 ]
Yu, Li [1 ]
机构
[1] Shenzhen Univ, Shenzhen Univ Clin Med Acad, Shenzhen Univ Gen Hosp,Hlth Sci Ctr,Dept Hematol, Shenzhen Key Lab Precis Med Hematol Malignancies, Shenzhen, Peoples R China
[2] Shenzhen Univ Gen Hosp, Cent Lab, Shenzhen, Peoples R China
来源
FRONTIERS IN ONCOLOGY | 2022年 / 12卷
基金
中国国家自然科学基金;
关键词
acute myeloid leukemia; TCR-T cells; immunotherapy; allo-HSCT; immune escape; CHRONIC LYMPHOCYTIC-LEUKEMIA; TUMOR-ASSOCIATED ANTIGEN; MHC CLASS-II; GENE-THERAPY; GAMMA-DELTA; CANCER/TESTIS ANTIGENS; ADOPTIVE IMMUNOTHERAPY; CANCER REGRESSION; RELAPSED AML; CORD BLOOD;
D O I
10.3389/fonc.2022.787108
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The cytogenetic abnormalities and molecular mutations involved in acute myeloid leukemia (AML) lead to unique treatment challenges. Although adoptive T-cell therapies (ACT) such as chimeric antigen receptor (CAR) T-cell therapy have shown promising results in the treatment of leukemias, especially B-cell malignancies, the optimal target surface antigen has yet to be discovered for AML. Alternatively, T-cell receptor (TCR)-redirected T cells can target intracellular antigens presented by HLA molecules, allowing the exploration of a broader territory of new therapeutic targets. Immunotherapy using adoptive transfer of WT1 antigen-specific TCR-T cells, for example, has had positive clinical successes in patients with AML. Nevertheless, AML can escape from immune system elimination by producing immunosuppressive factors or releasing several cytokines. This review presents recent advances of antigen-specific TCR-T cells in treating AML and discusses their challenges and future directions in clinical applications.
引用
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页数:18
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