| Literature DB >> 30691374 |
Mathias Vormehr1,2, Özlem Türeci1, Ugur Sahin1,2,3.
Abstract
T cells are key effectors of anticancer immunity. They are capable of distinguishing tumor cells from normal ones by recognizing major histocompatibility complex-bound cancer-specific peptides. Accumulating evidence suggests that peptides associated with T cell-mediated tumor rejection arise predominantly from somatically mutated proteins and are unique to every patient's tumor. Knowledge of an individual's cancer mutanome (the entirety of cancer mutations) allows harnessing this enormous tumor cell-specific repertoire of highly immunogenic antigens for individualized cancer vaccines. This review outlines the preclinical and clinical state of individualized cancer vaccine development and the challenges ahead.Entities:
Keywords: T cells; cancer; immunotherapy; individualized therapy; vaccines
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Year: 2019 PMID: 30691374 DOI: 10.1146/annurev-med-042617-101816
Source DB: PubMed Journal: Annu Rev Med ISSN: 0066-4219 Impact factor: 13.739