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- W2154966612 abstract "It is recognized that host response following viral infection is characterized by immunodominance, but deciphering the different factors contributing to immunodominance has proved a challenge due to concurrent expression of multiple MHC class I alleles. To address this, we generated H2-K−/−/D−/− double-knockout transgenic mice expressing either one or two human MHC-I alleles. We hypothesized that co-expression of different allele combinations figures critically in immunodominance and examined this in influenza-infected, double Tg MHC-I mice. In A2/B7 or A2/B27 mice, using ELISpot assays with the A2-restricted matrix I.58–66, the B7-restricted NP418–426 or the B27-restricted NP383–391 influenza A (flu) epitopes, we observed the expected recognition of both peptides for both alleles. In contrast, in flu-infected B7/B27 mice, a significantly reduced level of B27/NP383-restricted CTL response was detected while there was no change in the B7/NP418-restricted CTL response. Flu-specific tetramer studies revealed a partial deletion of Vβ8.1+ NP383/B27-restricted CD8+ T cells, and a diminished Vβ12+ CD8+ T-cell expansion in B7/B27 Tg mice. Using HLA Tg chimeric mice, we confirmed these findings. These findings shed light on the immune consequences of co-dominant expression of MHC-I alleles for host immune response to pathogens." @default.
- W2154966612 created "2016-06-24" @default.
- W2154966612 creator A5028232629 @default.
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- W2154966612 date "2013-10-20" @default.
- W2154966612 modified "2023-09-27" @default.
- W2154966612 title "Co-expression of HLA-B7 and HLA-B27 alleles is associated with B7-restricted immunodominant responses following influenza infection" @default.
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- W2154966612 doi "https://doi.org/10.1002/eji.201343597" @default.
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