HLArestrictor-a tool for patient-specific predictions of HLA restriction elements and optimal epitopes within peptides

被引:46
作者
Larsen, Malene Erup [1 ]
Kloverpris, Henrik [2 ]
Stryhn, Anette [3 ]
Koofhethile, Catherine K. [2 ]
Sims, Stuart [2 ]
Ndung'u, Thumbi [4 ,5 ,6 ]
Goulder, Philip [2 ]
Buus, Soren [3 ]
Nielsen, Morten [1 ]
机构
[1] Tech Univ Denmark, Ctr Biol Sequence Anal, DTU Syst Biol, DK-2800 Lyngby, Denmark
[2] Univ Oxford, Oxford OX1 3SY, England
[3] Univ Copenhagen, Expt Immunol Lab, Fac Hlth Sci, Copenhagen, Denmark
[4] Univ KwaZulu Natal, HIV Pathogenesis Programme, Doris Duke Med Res Inst, Durban, South Africa
[5] Massachusetts Gen Hosp, Ragon Inst, MIT, Charlestown, MA 02129 USA
[6] Harvard Univ, Charlestown, MA 02129 USA
关键词
HLA restriction; Epitope prediction; MHC class I; Peptide binding; T cell epitope validation; HLA tetramer validation; MAJOR HISTOCOMPATIBILITY COMPLEX; T-CELL RESPONSES; BINDING-AFFINITY; VACCINIA VIRUS; HIV;
D O I
10.1007/s00251-010-0493-5
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Traditionally, T cell epitope discovery requires considerable amounts of tedious, slow, and costly experimental work. During the last decade, prediction tools have emerged as essential tools allowing researchers to select a manageable list of epitope candidates to test from a larger peptide, protein, or even proteome. However, no current tools address the complexity caused by the highly polymorphic nature of the restricting HLA molecules, which effectively individualizes T cell responses. To fill this gap, we here present an easy-to-use prediction tool named HLArestrictor (http://www.cbs.dtu.dk/services/HLArestrictor), which is based on the highly versatile and accurate NetMHCpan predictor, which here has been optimized for the identification of both the MHC restriction element and the corresponding minimal epitope of a T cell response in a given individual. As input, it requires high-resolution (i.e., 4-digit) HLA typing of the individual. HLArestrictor then predicts all 8-11mer peptide binders within one or more larger peptides and provides an overview of the predicted HLA restrictions and minimal epitopes. The method was tested on a large dataset of HIV IFN gamma ELIspot peptide responses and was shown to identify HLA restrictions and minimal epitopes for about 90% of the positive peptide/patient pairs while rejecting more than 95% of the negative peptide-HLA pairs. Furthermore, for 18 peptide/HLA tetramer validated responses, HLArestrictor in all cases predicted both the HLA restriction element and minimal epitope. Thus, HLArestrictor should be a valuable tool in any T cell epitope discovery process aimed at identifying new epitopes from infectious diseases and other disease models.
引用
收藏
页码:43 / 55
页数:13
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