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An unnamed, preclinical **replication-competent oncolytic adenovirus** engineered to locally express a transforming growth factor-beta blocker and interferon-gamma. The vector is being investigated by the University of Minnesota as an intratumoral viro-immunotherapy for pancreatic ductal adenocarcinoma. It is intended to combine adenovirus-mediated tumor-cell lysis with reversal of TGF-beta-associated immunosuppression and fibrosis, plus IFN-gamma-driven immune activation. In mouse pancreatic cancer models, the dual-transgene vector produced greater antitumor activity than single-transgene constructs, induced immune-cell infiltration, reduced fibrosis, generated abscopal activity, and enhanced responses when combined with CAR-T cells.
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