Efficacy and safety of CAR19/22 T-cell cocktail therapy in patients with refractory/relapsed B-cell malignancies

Author:

Wang Na12,Hu Xuelian12,Cao Wenyue12,Li Chunrui12,Xiao Yi12,Cao Yang12,Gu Chaojiang34,Zhang Shangkun4,Chen Liting12ORCID,Cheng Jiali12,Wang Gaoxiang12,Zhou Xiaoxi12,Zheng Miao12,Mao Xia12,Jiang Lijun12,Wang Di12,Wang Qiuxiang12,Lou Yaoyao12,Cai Haodong12,Yan Dandan5,Zhang Yicheng12,Zhang Tongcun34,Zhou Jianfeng12,Huang Liang12ORCID

Affiliation:

1. Department of Hematology, Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, China;

2. Immunotherapy Research Center for Hematologic Diseases of Hubei Province, Wuhan, China;

3. College of Life Science and Health, Wuhan University of Science and Technology, Wuhan, China;

4. Wuhan Bio-Raid Biotechnology Co., Ltd., Wuhan, China; and

5. Department of Health Toxicology, Ministry of Education (MOE) Key Laboratory of Environment and Health, School of Public Health, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, China

Abstract

Relapse following chemeric antigen receptor (CAR) T-cell therapy can arise from progressive loss of the CAR T cells or from loss of the target antigen by tumor cells. Wang et al report that using a mix of CAR T cells targeting CD19 and CD22 reduces relapse with antigen-negative tumor cells. However, a lack of CAR T-cell persistence leads to increased relapse with antigen-positive cells.

Publisher

American Society of Hematology

Subject

Cell Biology,Hematology,Immunology,Biochemistry

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