Figure 5
Figure 5. Inefficient recognition of the L268M mutant by public TRBV4-3/TRBJ1-3 clonotypes. (A) In vivo dominance of public TRBV4-3/TRBJ1-3 clonotypes and prevalent viral variants at the time of sampling. *Codominant viral KK10 sequences. (B) Ag sensitivity of representative CD8+ T-cell clones for the wt KK10 and L268M mutant epitopes was measured in Cr51 cytotoxicity assays using EBV-transformed HLA-B*2705+ B cells pulsed with the corresponding peptides across a range of concentrations. (C) Suppression of HIV replication in HLA-B*2705+ CD4+ T cells infected with wt (HIVNL4-3) virus (■) or a mutant virus encoding the L268M epitope mutation () by representative CD8+ T-cell clones at 3 different E:T ratios. The percentage of p24+ CD4+ T cells was measured by flow cytometry at day 3 postinfection.

Inefficient recognition of the L268M mutant by public TRBV4-3/TRBJ1-3 clonotypes. (A) In vivo dominance of public TRBV4-3/TRBJ1-3 clonotypes and prevalent viral variants at the time of sampling. *Codominant viral KK10 sequences. (B) Ag sensitivity of representative CD8+ T-cell clones for the wt KK10 and L268M mutant epitopes was measured in Cr51 cytotoxicity assays using EBV-transformed HLA-B*2705+ B cells pulsed with the corresponding peptides across a range of concentrations. (C) Suppression of HIV replication in HLA-B*2705+ CD4+ T cells infected with wt (HIVNL4-3) virus (■) or a mutant virus encoding the L268M epitope mutation () by representative CD8+ T-cell clones at 3 different E:T ratios. The percentage of p24+ CD4+ T cells was measured by flow cytometry at day 3 postinfection.

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