期刊:Science [American Association for the Advancement of Science (AAAS)] 日期:2020-01-23卷期号:367 (6476): 401.5-402
标识
DOI:10.1126/science.367.6476.401-e
摘要
Cancer Immunotherapy
Chimeric antigen receptor (CAR)–T cells have been clinically effective in killing certain hematological malignancies, but achieving long-term patient responses for solid tumors remains a challenge. Reinhard et al. describe a two-part “CARVac” strategy to overcome poor CAR-T cell stimulation and responses in vivo. They introduce the tight junction protein claudin 6 (CLDN6) as a new CAR-T cell target and designed a nanoparticulate RNA vaccine encoding a chimeric receptor directed toward CLDN6. This lipoplex RNA vaccine promotes CLDN6 expression on the surface of dendritic cells, which in turn stimulates and enhances the efficacy of CLDN6-CAR-T cells for improved tumor therapy.
Science , this issue p. [446][1]
[1]: /lookup/doi/10.1126/science.aay5967