| Literature DB >> 31672285 |
Changwen Deng1, Jingjing Zhao1, Shixin Zhou1, Jiebin Dong1, Jixiang Cao1, Junshuang Gao1, Yun Bai2, Hongkui Deng3.
Abstract
Chimeric antigen receptor (CAR) T cell therapy remains relatively ineffective against solid tumors due to inadequate infiltration and in vivo expansion of CAR-T cells. Unlike hematological malignancies, solid tumors have vascular barriers that hinder CAR-T cells from reaching the tumor site. Here, we demonstrated that combretastatin A-4 phosphate (CA4P), a vascular disrupting agent (VDA), can significantly improve the infiltration ability of CAR-T cells in solid tumors as evidenced by elevated levels of IFN-γ. Moreover, combined treatment with CA4P and CAR-T cells greatly increased the therapeutic efficiency of the CAR-T cells in subcutaneous ovarian cancer mouse xenograft models and patient-derived xenograft (PDX) models of colon and ovarian carcinoma. Our findings highlight CA4P as an effective antitumor agent candidate for combination with CAR-T cells in clinical applications to treat solid tumors.Entities:
Keywords: chimeric antigen receptor; combretastatin A-4 phosphate; solid tumors; vascular disrupting agent
Year: 2019 PMID: 31672285 PMCID: PMC6953963 DOI: 10.1016/j.ymthe.2019.10.010
Source DB: PubMed Journal: Mol Ther ISSN: 1525-0016 Impact factor: 11.454