Figure 1.
Figure 1. Expression of CD4, HIV p24 antigen, and MHC class I molecules on HIV-infected primary CD4- T-cell blasts. HIV-1SF162-infected primary T-cell blasts were depleted of CD4+ cells before their use as target cells in the cytotoxicity assay. CD4-depleted HIV-infected cells (bold lines) were stained with fluorochrome-conjugated anti-CD4 antibody (A,C) or human anti-HIV p24 antibody, together with fluorochrome-conjugated goat anti-human IgG antibody (B,D). Cells were then stained with fluorochrome-conjugated anti-MHC class I antibody (C-D). As controls, uninfected CD4+ T cells (thin solid lines) were also stained with the same antibody. MHC class I molecules expressed on 104 uninfected CD4+ control cells (C-D), 104 HIV p24 antigen-positive cells (D), and 104 CD4- cells (C) were determined. Dotted lines indicate isotype control antibody (Ab).

Expression of CD4, HIV p24 antigen, and MHC class I molecules on HIV-infected primary CD4- T-cell blasts. HIV-1SF162-infected primary T-cell blasts were depleted of CD4+ cells before their use as target cells in the cytotoxicity assay. CD4-depleted HIV-infected cells (bold lines) were stained with fluorochrome-conjugated anti-CD4 antibody (A,C) or human anti-HIV p24 antibody, together with fluorochrome-conjugated goat anti-human IgG antibody (B,D). Cells were then stained with fluorochrome-conjugated anti-MHC class I antibody (C-D). As controls, uninfected CD4+ T cells (thin solid lines) were also stained with the same antibody. MHC class I molecules expressed on 104 uninfected CD4+ control cells (C-D), 104 HIV p24 antigen-positive cells (D), and 104 CD4- cells (C) were determined. Dotted lines indicate isotype control antibody (Ab).

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