While the irrelevant DsiRNA placebo had no significant effect on the tumor immune compartment, DCR-BCAT treatment resulted in highly significant increases in total T cells (CD3), cytotoxic T cells (CD8), antigen-presenting dendritic cells (CD103), and the PD-1 T cell checkpoint.
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RNAi-Mediated β-Catenin Inhibition Promotes T Cell Infiltration and Antitumor Activity in Combination with Immune Checkpoint Blockade.
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