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ANT308 PEG is a long-acting, PEGylated peptide antagonist of the vasoactive intestinal peptide (VIP) receptor. VIP is an immunosuppressive neuropeptide that is overexpressed in certain cancers, including acute myeloid leukemia (AML), where it functions as an alternative immune checkpoint. By inhibiting VIP receptor signaling, ANT308 PEG promotes T-cell activation, enhances the expression of effector markers such as Ki67 and TCF1, and increases the presence of chemokine receptors (CXCR3, CX3CR1) associated with tumor homing. In preclinical murine AML models, ANT308 PEG demonstrated superior anti-leukemia activity and improved survival compared to the non-PEGylated parent peptide, particularly when used in combination with PD-1 blockade.
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