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Anti-mesothelin CAR-T immunotherapy in patients with ovarian cancer.
Chen, Jiannan; Hu, Jianhua; Gu, Lili; Ji, Feng; Zhang, Fan; Zhang, Miaomiao; Li, Jun; Chen, Zhengliang; Jiang, Longwei; Zhang, Yan; Shi, Ruifang; Ma, Lihua; Jia, Shaochang; Zhang, Ying; Zhang, Qi; Liang, Junqing; Yao, Shunyu; Hu, Zhigang; Guo, Zhigang.
  • Chen J; Jiangsu Key Laboratory for Molecular and Medical Biotechnology, College of Life Sciences, Nanjing Normal University, Nanjing, 210023, China.
  • Hu J; Department of Biotherapy, Jinling Hospital of Nanjing University School of Medicine, Nanjing, 210002, China.
  • Gu L; Jiangsu Key Laboratory for Molecular and Medical Biotechnology, College of Life Sciences, Nanjing Normal University, Nanjing, 210023, China.
  • Ji F; Jiangsu Key Laboratory for Molecular and Medical Biotechnology, College of Life Sciences, Nanjing Normal University, Nanjing, 210023, China.
  • Zhang F; Jiangsu Key Laboratory for Molecular and Medical Biotechnology, College of Life Sciences, Nanjing Normal University, Nanjing, 210023, China.
  • Zhang M; Jiangsu Key Laboratory for Molecular and Medical Biotechnology, College of Life Sciences, Nanjing Normal University, Nanjing, 210023, China.
  • Li J; Nanjing Blue Shield Biotechnology Co., Ltd., Nanjing, 210023, China.
  • Chen Z; Nanjing Blue Shield Biotechnology Co., Ltd., Nanjing, 210023, China.
  • Jiang L; Department of Biotherapy, Jinling Hospital of Nanjing University School of Medicine, Nanjing, 210002, China.
  • Zhang Y; Department of Biotherapy, Jinling Hospital of Nanjing University School of Medicine, Nanjing, 210002, China.
  • Shi R; Department of Biotherapy, Jinling Hospital of Nanjing University School of Medicine, Nanjing, 210002, China.
  • Ma L; Department of Biotherapy, Jinling Hospital of Nanjing University School of Medicine, Nanjing, 210002, China.
  • Jia S; Department of Biotherapy, Jinling Hospital of Nanjing University School of Medicine, Nanjing, 210002, China.
  • Zhang Y; Department of Pathology, Jinling Hospital of Nanjing University School of Medicine, Nanjing, 210002, China.
  • Zhang Q; Center of Interventional Radiology and Vascular Surgery, Department of Radiology, Zhongda Hospital, Medical School, Southeast University, Nanjing, 210009, China.
  • Liang J; Inner Mongolia Autonomous Region Cancer Hospital, Hohhot, 010010, China.
  • Yao S; Baylor University, 1311 S 5th St, Waco, USA.
  • Hu Z; Jiangsu Key Laboratory for Molecular and Medical Biotechnology, College of Life Sciences, Nanjing Normal University, Nanjing, 210023, China. huzg_2000@126.com.
  • Guo Z; Jiangsu Key Laboratory for Molecular and Medical Biotechnology, College of Life Sciences, Nanjing Normal University, Nanjing, 210023, China. guo@njnu.edu.cn.
Cancer Immunol Immunother ; 72(2): 409-425, 2023 Feb.
Article en En | MEDLINE | ID: mdl-35925286
ABSTRACT
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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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Neoplasias Ováricas / Inmunoterapia Adoptiva / Receptores Quiméricos de Antígenos Límite: Animals / Female / Humans Idioma: En Año: 2023 Tipo del documento: Article

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Neoplasias Ováricas / Inmunoterapia Adoptiva / Receptores Quiméricos de Antígenos Límite: Animals / Female / Humans Idioma: En Año: 2023 Tipo del documento: Article