| Literature DB >> 31582530 |
Jinsheng Han1, Fei Gao1,2, Songsong Geng3, Xueshuai Ye1,3, Tie Wang4, Pingping Du3, Ziqi Cai3, Zexian Fu3,5, Zhilong Zhao3,6, Long Shi3,7, Qingxia Li2, Jianhui Cai8,2,3.
Abstract
Viral-based chimeric antigen receptor-engineered T (CAR T)-cell manufacturing has potential safety risks and relatively high costs. The nonviral minicircle DNA (mcDNA) is safer for patients, cheaper to produce, and may be a more suitable technique to generate CAR T cells. In this study, we produced mcDNA-based CAR T cells specifically targeting prostate stem cell antigen (PSCA; mcDNA-PSCA-CAR T cells). Our results showed that mcDNA-PSCA-CAR T cells persisted in mouse peripheral blood as long as 28 days and demonstrated more CAR T-cell infiltration, higher cytokine secretion levels, and better antitumor effects. Together, our results suggest that mcDNA-CAR can be a safe and cost-effective platform to produce CAR T cells. ©2019 American Association for Cancer Research.Entities:
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Year: 2019 PMID: 31582530 DOI: 10.1158/1535-7163.MCT-19-0204
Source DB: PubMed Journal: Mol Cancer Ther ISSN: 1535-7163 Impact factor: 6.261