TY - JOUR
T1 - Identification of immunogenic consensus T-cell epitopes in globally distributed influenza-A H1N1 neuraminidase
AU - Gupta, Shishir K.
AU - Srivastava, Mugdha
AU - Akhoon, Bashir A.
AU - Smita, Suchi
AU - Schmitz, Ulf
AU - Wolkenhauer, Olaf
AU - Vera, Julio
AU - Gupta, Shailendra K.
PY - 2011/3
Y1 - 2011/3
N2 - 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 FSYKYGNGV was identified as a highly conserved, immunogenic and potential vaccine candidate, capable for generating both CD8+ and CD4+ responses.
AB - 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 FSYKYGNGV was identified as a highly conserved, immunogenic and potential vaccine candidate, capable for generating both CD8+ and CD4+ responses.
KW - Epitope prediction
KW - H1N1
KW - Neuraminidase
KW - Swine influenza
UR - https://www.scopus.com/pages/publications/79951944884
U2 - 10.1016/j.meegid.2010.10.013
DO - 10.1016/j.meegid.2010.10.013
M3 - Article
C2 - 21094280
AN - SCOPUS:79951944884
SN - 1567-1348
VL - 11
SP - 308
EP - 319
JO - Infection, Genetics and Evolution
JF - Infection, Genetics and Evolution
IS - 2
ER -