Acute lymphoblastic leukemia relapse after CD19-targeted chimeric antigen receptor T cell therapy

被引:41
作者
Wang, Jiasheng [1 ]
Hu, Yongxian [1 ]
Huang, He [1 ]
机构
[1] Zhejiang Univ, Bone Marrow Transplantat Ctr, Affiliated Hosp 1, Sch Med, Hangzhou, Zhejiang, Peoples R China
关键词
immunotherapy; CAR T cell; bone marrow microenvironment; T cell exhaustion; checkpoint inhibitors; B-CELL; SIGNAL-TRANSDUCTION; ANTITUMOR EFFICACY; LINEAGE SWITCH; CAR; IMMUNOTHERAPY; MALIGNANCIES; RESISTANCE; PROLIFERATION; MUTATIONS;
D O I
10.1189/jlb.5RU0817-315R
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
CART19 therapy has revolutionized the treatment of CD19(+) acute lymphoblastic leukemia, demonstrating an unprecedented complete remission rate; however, as follow-up prolongs, a high relapse rate after CART19 therapy has emerged as one of the major problems. Relapse can be attributed to the loss of leukemic cell immunogenicity, diminished function and amount of CART19 cells, and the inhibitory bone marrow microenvironment. Although studies to prevent and treat relapse have begun, some encouraging results have demonstrated the possibility of decreasing the relapse rate. In this review, we focus on the possible mechanisms behind relapse. We will summarize and propose strategies to prevent and manage relapse on the basis of these potential mechanisms.
引用
收藏
页码:1347 / 1356
页数:10
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