Haploidentical CD19/CD22 bispecific CAR-T cells induced MRD-negative remission in a patient with relapsed and refractory adult B-ALL after haploidentical hematopoietic stem cell transplantation

被引:48
|
作者
Jia, Hejin [1 ]
Wang, Zhenguang [1 ]
Wang, Yao [1 ]
Liu, Yang [2 ]
Dai, Hanren [1 ]
Tong, Chuan [1 ]
Guo, Yelei [1 ]
Guo, Bo [2 ]
Ti, Dongdong [1 ]
Han, Xiao [1 ]
Yang, Qingming [1 ]
Wu, Zhiqiang [1 ]
Han, Weidong [1 ]
机构
[1] Chinese Peoples Liberat Army Gen Hosp, Biotherapeut Dept, Mol & Immunol Dept, 28 Fuxing Rd, Beijing 100853, Peoples R China
[2] Chinese Peoples Liberat Army Gen Hosp, Dept Geriatr Hematol, 28 Fuxing Rd, Beijing 100853, Peoples R China
基金
中国国家自然科学基金;
关键词
Chimeric antigen receptor; CAR-T; Bispecific CAR-T; GVHD; Haploidentical CAR-T; VERSUS-HOST-DISEASE; PHASE-I; GRAFT; INFUSION; LEUKEMIA; CHILDREN;
D O I
10.1186/s13045-019-0741-6
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
BackgroundChimeric antigen receptor T (CAR-T) cell therapy simultaneously against CD19 and CD22 is an attractive strategy to address the antigen escape relapse after CD19-directed CAR-T cell therapies. However, the potential of optimizing the durability of remission by this approach in patients with B cell acute lymphoblastic leukemia (B-ALL) remains a critical unanswered question so far.Case presentationWe treated an adult patient with relapsed and refractory B-ALL after haploidentical hematopoietic stem cell transplantation (HSCT) by administering haploidentical CAR-T cells targeting both CD19 and CD22 following preparative lymphodepleting chemotherapy. This patient has remained in minimal residual disease-negative remission for more than 14months and has been tapered off graft versus host disease prophylaxis.ConclusionsCAR simultaneously targeting CD19 and CD22 has the potential of inducing long-term remission in patients with B-ALL.
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页数:9
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