Identification of immunogenic consensus T-cell epitopes in globally distributed influenza-A H1N1 neuraminidase

被引:23
作者
Gupta, Shishir K. [1 ]
Srivastava, Mugdha [1 ]
Akhoon, Bashir A. [2 ]
Smita, Suchi [3 ]
Schmitz, Ulf [4 ]
Wolkenhauer, Olaf [4 ]
Vera, Julio [4 ]
Gupta, Shailendra K. [4 ,5 ]
机构
[1] Soc Biol Res & Rural Dev, Lucknow 226010, UP, India
[2] SMVD Univ, Ctr Bioinformat, Dept Biotechnol, Jammu, India
[3] Integral Univ, Dept Bioinformat, Lucknow, UP, India
[4] Univ Rostock, D-2500 Rostock 1, Germany
[5] CSIR, Indian Inst Toxicol Res, Lucknow, Uttar Pradesh, India
关键词
H1N1; Neuraminidase; Epitope prediction; Swine influenza; DE-NOVO PEPTIDE; CLASS-I; BINDING-AFFINITY; VIRUS; PREDICTION; ALIGNMENT; COMPLEX; SPECIFICITIES; OPTIMIZATION; TUBERCULOSIS;
D O I
10.1016/j.meegid.2010.10.013
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
Antigenic drift is the ability of the swine influenza virus to undergo continuous and progressive changes in response to the host immune system. These changes dictate influenza vaccine updates annually to ensure inclusion of antigens of the most current strains. The identification of those peptides that stimulate T-cell responses, termed T-cell epitopes, is essential for the development of successful vaccines. In this study, the highly conserved and specific epitopes from neuraminidase of globally distributed H1N1 strains were predicted so that these potential vaccine candidates may escape with antigenic drift. A total of nine novel CD8(+) T-cell epitopes for MHC class-I and eight novel CD4(+) T-cell epitopes for MHC class-II alleles were proposed as novel epitope based vaccine candidates. Additionally, the epitope FSYKYGNCV was identified as a highly conserved, immunogenic and potential vaccine candidate, capable for generating both CD8(+) and CD4(+) responses. (c) 2010 Elsevier B.V. All rights reserved.
引用
收藏
页码:308 / 319
页数:12
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