Abstract

Adoptive T-cell therapy using tumor-infiltrating lymphocytes (TIL) has demonstrated that potent and long-lasting antitumor responses can be achieved with cellular cancer immunotherapy in solid tumor patients. Yet, the therapy yields various toxicities, due to toxic lymphodepleting preconditioning and IL-2 postconditioning. With the intent of decreasing conditioning-related toxicities, while retaining efficacy, we developed TILT-123 (Ad5/3-E2F-D24-hTNFa-IRES-hIL2), a novel oncolytic adenovirus designed to reinvigorate antitumor T-cells.

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