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Frameshift mutations, neoantigens and tumor-specific CD8(+) T cells in microsatellite unstable colorectal cancers
Pauline Maby1, Jérôme Galon2, Jean-Baptiste Latouche3
1Inserm U1079, Institute for Research and Innovation in Biomedecine (IRIB), Rouen, France; Inserm U872, Laboratory of Integrative Cancer Immunology, Paris, France; Université Paris Descartes, Paris, France; Cordeliers Research Center, Université Pierre et Marie Curie, Paris 6, Paris, France.
Abstract:
Microsatellite unstable colorectal cancers (CRC) express frameshift mutation-derived tumor-specific neoantigens. We recently showed that: (i) frameshift mutations were correlated with tumor-infiltrating CD8(+) T cell density, (ii) neoantigen-specific cytotoxic T cells could be obtained in patients whose tumors harbored these mutations, underlining the interest of developing personalized immunotherapy strategies in these cancers.
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