| Literature DB >> 29315598 |
Kamilla Kjaergaard Jensen1, Massimo Andreatta2, Paolo Marcatili1, Søren Buus3, Jason A Greenbaum4, Zhen Yan4, Alessandro Sette5,6, Bjoern Peters5,6, Morten Nielsen1,2.
Abstract
Major histocompatibility complex class II (MHC-II) molecules are expressed on the surface of professional antigen-presenting cells where they display peptides to T helper cells, which orchestrate the onset and outcome of many host immune responses. Understanding which peptides will be presented by the MHC-II molecule is therefore important for understanding the activation of T helper cells and can be used to identify T-cell epitopes. We here present updated versions of two MHC-II-peptide binding affinity prediction methods, NetMHCII and NetMHCIIpan. These were constructed using an extended data set of quantitative MHC-peptide binding affinity data obtained from the Immune Epitope Database covering HLA-DR, HLA-DQ, HLA-DP and H-2 mouse molecules. We show that training with this extended data set improved the performance for peptide binding predictions for both methods. Both methods are publicly available at www.cbs.dtu.dk/services/NetMHCII-2.3 and www.cbs.dtu.dk/services/NetMHCIIpan-3.2.Entities:
Keywords: MHC binding specificity; T-cell epitope; affinity predictions; immunogenic peptides; peptide-MHC binding
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Year: 2018 PMID: 29315598 PMCID: PMC6002223 DOI: 10.1111/imm.12889
Source DB: PubMed Journal: Immunology ISSN: 0019-2805 Impact factor: 7.397