Recent progress in chimeric antigen receptor therapy for acute myeloid leukemia

被引:1
作者
Wang, Xiangyu [1 ]
Zhang, Yanming [1 ]
Xue, Shengli [2 ]
机构
[1] Xuzhou Med Univ, Huaian Hosp, Huaian Peoples Hosp 2, Dept Hematol, Huaian 223002, Peoples R China
[2] Soochow Univ, Affiliated Hosp 1, Jiangsu Inst Hematol, Natl Clin Res Ctr Hematol Dis, Suzhou 215006, Peoples R China
基金
国家重点研发计划; 中国国家自然科学基金;
关键词
Chimeric antigen receptor; Acute myeloid leukemia; Immunotherapy; Targeted therapy; MODIFIED T-CELLS; GEMTUZUMAB OZOGAMICIN; ALPHA CHAIN; CAR; IMMUNOTHERAPY; EXPRESSION; TARGET; NKG2D; FLT3; GENE;
D O I
10.1007/s00277-023-05601-y
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Although CAR-T cell therapy has been particularly successful as a treatment for B cell malignancies, effectively treating acute myeloid leukemia with CAR remains a greater challenge. Multiple preclinical studies and clinical trials are underway, including on AML-related surface markers that CAR-T cells can target, such as CD123, CD33, NKG2D, CLL1, CD7, FLT3, Lewis Y and CD70, all of which provide opportunities for developing CAR-T therapies with improved specificity and efficacy. We also explored specific strategies for CAR-T cell treatment of AML, including immune checkpoints, suicide genes, dual targeting, genomic tools and the potential for universal CAR. In addition, CAR-T cell therapy for AML still has certain risks and challenges, including cytokine release syndrome (CRS) and haematotoxicity. Despite these challenges, as a new targeting method for AML treatment, CAR-T cell therapy still has great prospects. Ongoing research aims to further optimize this treatment mode.
引用
收藏
页码:1843 / 1857
页数:15
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