间皮素
卵巢癌
医学
免疫疗法
癌症研究
细胞因子
癌症
过继性细胞移植
抗原
嵌合抗原受体
肿瘤科
免疫学
T细胞
内科学
免疫系统
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
标识
DOI:10.1007/s00262-022-03238-w
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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