Neoantigens encoded in the cancer genome.

Abstract:

:Somatic mutations in the genome represent one of the major drivers of malignancy. However, non-synonymous mutations are also a source of mutated peptides that are presented by HLA molecules to induce protective CD4 and CD8 T cell responses. Consistent with this notion, the mutation burden of a tumor is correlated with local immunity as well as outcome of therapy and patient survival. Furthermore, neoantigen-specific T cells appear sufficient to control tumors prophylactically and therapeutically. While the role of neoantigens as a determinant of the foreignness of human cancers is now well established, major questions, including the relative importance of clonal vs subclonal neoantigens, and CD4 vs CD8 T cells, remain unanswered. We expect continued animal studies to address some of the open issues and ongoing clinical trials to establish the utility of therapeutic strategies to enhance neoantigen-specific T cell responses in human cancer.

journal_name

Curr Opin Immunol

authors

Schumacher TN,Hacohen N

doi

10.1016/j.coi.2016.07.005

subject

Has Abstract

pub_date

2016-08-01 00:00:00

pages

98-103

eissn

0952-7915

issn

1879-0372

pii

S0952-7915(16)30071-1

journal_volume

41

pub_type

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