| Literature DB >> 27928884 |
Frances-Rose Schumacher1, Lélia Delamarre2, Suchit Jhunjhunwala3, Zora Modrusan4, Qui T Phung5, Joshua E Elias6, Jennie R Lill1.
Abstract
Major histocompatibility complex Class I (MHCI) and Class II (MHCII) presented peptides powerfully modulate T cell immunity and play a vital role in generating effective anti-tumor and anti-viral immune responses in mammals. Characterizing these MHCI or MHCII presented peptides can help generate therapeutic treatments, afford information on T cell mediated biomarkers, provide insight into disease progression, and reduce adverse anti-drug side effects from engineered biotherapeutics. Here, we explore the tools and techniques commonly employed to discover both MHCI- and MHCII-presented peptides. We describe complementary strategies that enhance the characterization of these peptides and the informatics tools employed for both predicting and characterizing MHCI- and MHCII-presented epitopes. The evolution of methodologies for isolating MHC-presented peptides is discussed, as are the mass spectrometric workflows that can be employed for their characterization. We provide a perspective on where this field is headed, and how these tools may be applicable to the discovery and monitoring of epitopes in a variety of scenarios.Entities:
Keywords: Biomedicine; Cancer vaccines; Major histocompatibility complex; Next generation sequencing; T cell epitope
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Year: 2017 PMID: 27928884 DOI: 10.1002/pmic.201600061
Source DB: PubMed Journal: Proteomics ISSN: 1615-9853 Impact factor: 3.984