Topics
Treatment, Outcomes / Survival, Side effects / Toxicity
Modality
Immunotherapy, Targeted therapy, Cell therapy, Imaging
Study type
Lab / Preclinical
Abstract
Immune checkpoint inhibitor (ICI) therapy has significantly improved the treatment of solid tumors such as hepatocellular carcinoma (HCC); however, most patients fail to respond. Here, we examined whether co-administration of the tumor-penetrating internalizing (i)RGD peptide, which selectively increases tumor vascular permeability in a neuropilin-1-dependent…
Authors
Jan Henrik Klug, Blerina Aliraj, Lucia Alcober-Boquet, Dominic Denk +10
AI-generated summary
Co-administered internalizing RGD peptide boosts anti-PD-L1 therapy in hepatocellular carcinoma. reports: Immune checkpoint inhibitor (ICI) therapy has significantly improved the treatment of solid tumors such as hepatocellular carcinoma (HCC); however, most patients fail to respond. Here, we examined whether co-administration of the tumor-penetrating internalizing (i)RGD peptide, which selectively increases tumor vascular permeability in a neuropilin-1-dependent manner, enhances intratumoral delivery and therapeutic efficacy of αPD-L1 in mouse models of HCC. αPD-L1, with or without iRGD, was administered intravenously to mice bearing endogenous HCCs (TGFα/c-myc and diethylnitrosamine [DEN]/carbon tetrachloride [CCl 4 ] models).
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Primary source: PubMed.