Recognition of homo- and heterosubtypic variants of influenza A viruses by human CD8+ T lymphocytes

被引:103
作者
Boon, ACM
de Mutsert, G
van Baarle, D
Smith, DJ
Lapedes, AS
Fouchier, RAM
Sintnicolaas, K
Osterhaus, ADME
Rimmelzwaan, GF
机构
[1] Erasmus MC, Inst Virol, Dept Virol, NL-3000 DR Rotterdam, Netherlands
[2] Erasmus MC, Inst Virol, WHO, Natl Influenza Ctr, NL-3000 DR Rotterdam, Netherlands
[3] Sanquin Res Cent Lab Bloodtransfus, Dept Clin Viroimmunol, Amsterdam, Netherlands
[4] Univ Cambridge, Dept Zool, Cambridge CB2 1TN, England
[5] Santa Fe Inst, Santa Fe, NM 87501 USA
[6] Los Alamos Natl Lab, Los Alamos, NM 87545 USA
[7] Lab Histocompatibil & Immungenet, Sanquin Bloodbank Rotterdam, Dordrecht, Netherlands
关键词
D O I
10.4049/jimmunol.172.4.2453
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
In the present study, the recognition of epitope variants of influenza A viruses by human CTL was investigated. To this end, human CD8(+) CTL clones, specific for natural variants of the HLA-B*3501-restricted epitope in the nucleoprotein (NP418-426), were generated. As determined in Cr-51 release assays and by flow cytometry with HLA-B*3501-peptide tetrameric complexes, CTL clones were found to be specific for epitopes within one subtype or cross-reactive with heterosubtypic variants of the epitope. Using eight natural variants of the epitope, positions in the 9-mer important for T cell recognition and involved in escape from CTL immunity were identified and visualized using multidimensional scaling. It was shown that positions 4 and 5 in the 9-mer epitope were important determinants of T cell specificity. The in vivo existence of CD8(+) cells cross-reactive with homo- and heterosubtypic variants of the epitope was further confirmed using polyclonal T cell populations obtained after stimulation of PBMC with different influenza A viruses. Based on the observed recognition patterns of the clonal and polyclonal T cell populations and serology, it is hypothesized that consecutive infections with influenza viruses containing different variants of the epitope select for cross-reactive T cells in vivo. The Journal of Immunology, 2004, 172: 2453-2460.
引用
收藏
页码:2453 / 2460
页数:8
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