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Nat Commun. 2017 Feb 13;8:14340. doi: 10.1038/ncomms14340.

Intratumoral modulation of the inducible co-stimulator ICOS by recombinant oncolytic virus promotes systemic anti-tumour immunity.

Author information

1
Department of Medicine, Memorial Sloan Kettering Cancer Center, New York, New York 10065, USA.
2
Weill Cornell Medical College, New York, New York 10065, USA.
3
Ludwig Collaborative Laboratory, Memorial Sloan Kettering Cancer Center, New York, New York 10065, USA.
4
Swim Across America Laboratory, Memorial Sloan Kettering Cancer Center, New York, New York 10065, USA.
5
Department of Microbiology, Icahn School of Medicine at Mount Sinai, New York, New York 10029, USA.
6
Department of Immunology, MD Anderson Cancer Center, Houston, Texas 77030, USA.

Abstract

Emerging data suggest that locoregional cancer therapeutic approaches with oncolytic viruses can lead to systemic anti-tumour immunity, although the appropriate targets for intratumoral immunomodulation using this strategy are not known. Here we find that intratumoral therapy with Newcastle disease virus (NDV), in addition to the activation of innate immunity, upregulates the expression of T-cell co-stimulatory receptors, with the inducible co-stimulator (ICOS) being most notable. To explore ICOS as a direct target in the tumour, we engineered a recombinant NDV-expressing ICOS ligand (NDV-ICOSL). In the bilateral flank tumour models, intratumoral administration of NDV-ICOSL results in enhanced infiltration with activated T cells in both virus-injected and distant tumours, and leads to effective rejection of both tumours when used in combination with systemic CTLA-4 blockade. These findings highlight that intratumoral immunomodulation with an oncolytic virus expressing a rationally selected ligand can be an effective strategy to drive systemic efficacy of immune checkpoint blockade.

PMID:
28194010
PMCID:
PMC5316835
DOI:
10.1038/ncomms14340
[Indexed for MEDLINE]
Free PMC Article

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