A second‐generation CD38‐CAR‐T cell for the treatment of multiple myeloma

Author:

Li Hongwen12,Li Jing3,Wu Jiazhuo124,Shi Zhuangzhuang124,Gao Yuyang124,Song Wenting124,Li Jiwei12,Li Zhaoming12,Zhang Mingzhi12ORCID

Affiliation:

1. Department of Oncology The First Affiliated Hospital of Zhengzhou University Zhengzhou China

2. State Key Laboratory of Esophageal Cancer Prevention and Treatment and Henan Key Laboratory for Esophageal Cancer Research The First Affiliated Hospital of Zhengzhou University Zhengzhou China

3. Department of Medical Oncology, State Key Laboratory of Oncology in South China, Collaborative Innovation Center for Cancer Medicine Sun Yat‐sen University Cancer Center Guangzhou China

4. Academy of Medical Sciences of Zhengzhou University Zhengzhou China

Abstract

AbstractBackgroundMultiple myeloma (MM) is an aggressive plasma cell malignancy, causing a number of deaths worldwide every year. Chimeric antigen receptor (CAR) transduced T‐cell therapy has been a promising immunotherapy against hematological malignancies.MethodsIn this study, we developed a second‐generation CAR construct and generated CAR‐T cells targeting CD38 molecule. Then effects of CAR‐T cells against MM cell lines were evaluated.ResultsCD38‐CAR‐T cells showed higher cytotoxicity to MM cell lines and primary MM cells than that of control T cells in vitro. Over 50% MM1.s and RPMI8226 cells were killed by CAR‐T cells even at effector to target ratio of 1:100. CAR‐T cells also showed an enhanced cytotoxicity against primary MM cells. CAR‐T cells could be activated and produced a variety of cytokines in a target‐dependent manner. In vivo test indicated that CAR‐T cells also showed significant antitumor effect on xenograft mice models.ConclusionThese results indicated a promising therapeutic strategy of CD38‐CAR‐T cells against MM.

Funder

National Natural Science Foundation of China

Publisher

Wiley

Subject

Cancer Research,Radiology, Nuclear Medicine and imaging,Oncology

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