Anti-mesothelin CAR-T immunotherapy in patients with ovarian cancer

被引:0
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作者
Jiannan Chen
Jianhua Hu
Lili Gu
Feng Ji
Fan Zhang
Miaomiao Zhang
Jun Li
Zhengliang Chen
Longwei Jiang
Yan Zhang
Ruifang Shi
Lihua Ma
Shaochang Jia
Ying Zhang
Qi Zhang
Junqing Liang
Shunyu Yao
Zhigang Hu
Zhigang Guo
机构
[1] Nanjing Normal University,Jiangsu Key Laboratory for Molecular and Medical Biotechnology, College of Life Sciences
[2] Jinling Hospital of Nanjing University School of Medicine,Department of Biotherapy
[3] Nanjing Blue Shield Biotechnology Co.,Department of Pathology
[4] Ltd.,Center of Interventional Radiology and Vascular Surgery, Department of Radiology, Zhongda Hospital, Medical School
[5] Jinling Hospital of Nanjing University School of Medicine,undefined
[6] Southeast University,undefined
[7] Inner Mongolia Autonomous Region Cancer Hospital,undefined
[8] Baylor University,undefined
来源
关键词
CAR-T; Mesothelin; Immunotherapy; Ovarian cancer; Investigator-initiated clinical trial;
D O I
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中图分类号
学科分类号
摘要
Recently, chimeric antigen receptor T cell (CAR-T) therapy has received increasing attention as an adoptive cellular immunotherapy that targets tumors. However, numerous challenges remain for the effective use of CAR-T to treat solid tumors, including ovarian cancer, which is an aggressive and metastatic cancer with a poor therapeutic response. We screened for an effective anti-MSLN single-chain Fv antibody with comparable binding activity and non-off-target properties using human phage display library. A second-generation of anti-MSLN CAR was designed and generated. We demonstrated the efficacy of our anti-MSLN CAR-T cells for ovarian cancer treatment in an in vitro experiment to kill ovarian tumor cell lines. The anti-MSLN CAR-T cells impeded MSLN-positive tumor growth concomitant with a significant increase in cytokine levels compared with the control. Then, we demonstrated the efficacy of anti-MSLN CAR-T cells in an in vivo experiment against ovarian cancer cell-derived xenografts. Furthermore, we herein report three cases with ovarian cancer who were treated with autologous anti-MSLN CAR-T cells and evaluate the safety and effectiveness of adoptive cell therapy. In this investigator-initiated clinical trials, no patients experienced cytokine release syndrome or neurological symptoms over 2 grads. Disease stabilized in two patients, with progression-free survival times of 5.8 and 4.6 months. Transient CAR expression was detected in patient blood after infusion each time. The tumor partially subsided, and the patient’s condition was relieved. In conclusion, this work proves the efficacy of the anti-MSLN CAR-T treatment strategy in ovarian cancer and provides preliminary data for the development of further clinical trials.
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页码:409 / 425
页数:16
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