Overcoming resistance to anti-CD19 CAR T-cell therapy in B-cell malignancies

被引:4
|
作者
Yang, Xingcheng [1 ,2 ]
Wei, Jia [1 ,2 ,3 ]
Zhou, Jianfeng [1 ,2 ]
机构
[1] Huazhong Univ Sci & Technol, Tongji Hosp, Dept Hematol, Tongji Med Coll, 1095 Jiefang Ave, Wuhan 430030, Hubei, Peoples R China
[2] Immunotherapy Res Ctr Hematol Dis Hubei Prov, Wuhan, Hubei, Peoples R China
[3] Huazhong Univ Sci & Technol, Dept Hematol, Shanxi Bethune Hosp,Tongji Med Coll, Shanxi Acad Med Sci,Shanxi Med Univ,Shanxi Tongji, Taiyuan, Peoples R China
基金
中国国家自然科学基金;
关键词
antigen escape; B-cell malignancy; CD19; chimeric antigen receptor; overcoming strategy; resistance; T cell exhaustion; CHIMERIC-ANTIGEN-RECEPTOR; MYELOID CELLS; PERIPHERAL-BLOOD; LINEAGE SWITCH; TUMOR-IMMUNITY; LEUKEMIA; LYMPHOMA; EFFICACY; ESCAPE; EXPRESSION;
D O I
10.1002/hon.3036
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Anti-CD19 chimeric antigen receptor (CAR) T-cell therapy has rapidly changed current treatment pattern, providing a better option for individuals with primary refractory or relapsed B-cell non-Hodgkin lymphoma (r/r B-NHL) and B-cell acute lymphoblastic leukemia (r/r B-ALL). However, despite the outstanding efficacy, a high relapse rate is still found in some B-cell malignancies after anti-CD19 CAR T-cell therapy, which emerges as a main barrier for improving the overall response and long-term outcomes. Understanding the resistance mechanism is crucial to improve current CAR T products, better incorporate them into the current therapy system and develop novel CAR approaches. Herein, we discuss the latest advances in understanding the mechanisms limiting efficacy of CAR T-cell therapy, resulting in CD19 negative (CD19(-)) and CD19 positive (CD19(+)) relapses. We also provide a whole scenario of current potential strategies to overcome these barriers.
引用
收藏
页码:821 / 834
页数:14
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