A Roadmap Toward the Definition of Actionable Tumor-Specific Antigens

被引:24
|
作者
Minati, Robin [1 ,2 ]
Perreault, Claude [2 ,3 ]
Thibault, Pierre [2 ,4 ]
机构
[1] Univ Lyon, Univ Claude Bernard Lyon 1, Ecole Normale Super Lyon, Lyon, France
[2] Univ Montreal, Inst Res Immunol & Canc, Montreal, PQ, Canada
[3] Univ Montreal, Dept Med, Montreal, PQ, Canada
[4] Univ Montreal, Dept Chem, Montreal, PQ, Canada
来源
FRONTIERS IN IMMUNOLOGY | 2020年 / 11卷
关键词
tumor-specific antigens; neoantigens; immunopeptidome; proteogenomics; alternative antigens; cancer immunotherapy; pan-cancer antigen research; MHC CLASS-I; CHRONIC MYELOGENOUS LEUKEMIA; CHRONIC MYELOID-LEUKEMIA; OPEN READING FRAME; T-CELL EPITOPES; MICROSATELLITE INSTABILITY; CITRULLINATED VIMENTIN; RHEUMATOID-ARTHRITIS; COLORECTAL CANCERS; GENE FUSIONS;
D O I
10.3389/fimmu.2020.583287
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
The search for tumor-specific antigens (TSAs) has considerably accelerated during the past decade due to the improvement of proteogenomic detection methods. This provides new opportunities for the development of novel antitumoral immunotherapies to mount an efficient T cell response against one or multiple types of tumors. While the identification of mutated antigens originating from coding exons has provided relatively few TSA candidates, the possibility of enlarging the repertoire of targetable TSAs by looking at antigens arising from non-canonical open reading frames opens up interesting avenues for cancer immunotherapy. In this review, we outline the potential sources of TSAs and the mechanisms responsible for their expression strictly in cancer cells. In line with the heterogeneity of cancer, we propose that discrete families of TSAs may be enriched in specific cancer types.
引用
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页数:15
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