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IFN-gamma is required for cytotoxic T cell-dependent cancer genome immunoediting


Genetic evolution that occurs during cancer progression enables tumour heterogeneity, thereby fostering tumour adaptation, therapeutic resistance and metastatic potential. Immune responses are known to select (immunoedit) tumour cells displaying immunoevasive properties. Here we address the role of IFN-gamma in mediating the immunoediting process. We observe that, in several mouse tumour models such as HA-expressing 4T1 mammary carcinoma cells, OVA-expressing EG7 lymphoma cells and CMS5 MCA-induced fibrosarcoma cells naturally expressing mutated extracellular signal-regulated kinase (ERK) antigen, the action of antigen-specific cytotoxic T cell (CTL) in vivo results in the emergence of resistant cancer cell clones only in the presence of IFN-gamma within the tumour microenvironment. Moreover, we show that exposure of tumours to IFN-gamma-producing antigen-specific CTLs in vivo results in copy-number alterations (CNAs) associated with DNA damage response and modulation of DNA editing/repair gene expression. These results suggest that enhanced genetic instability might be one of the mechanisms by which CTLs and IFN-gamma immunoedits tumours, altering their immune resistance as a result of genetic evolution.

Type Journal
ISBN 2041-1723 (Electronic) 2041-1723 (Linking)
Authors Takeda, K.; Nakayama, M.; Hayakawa, Y.; Kojima, Y.; Ikeda, H.; Imai, N.; Ogasawara, K.; Okumura, K.; Thomas, D. M.; Smyth, M. J.
Responsible Garvan Author Prof David Thomas
Publisher Name Nature Communications
Published Date 2017-02-24
Published Volume 8
Published Pages 14607
Status Published in-print
DOI 10.1038/ncomms14607
URL link to publisher's version
OpenAccess link to author's accepted manuscript version