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Abstract
The authors would like to correct panel H in Fig 3 to show the correct MFI values of PD-L1 expression on human CD4+ T cells. The error occurred during preparation of the figure for manuscript revision. The percentages of infected CD4 cells expressing PD-L1 were accidentally duplicated from panel I in Fig 3. Please see the corrected version of Fig 3 here. Fig 3 PD-L1 expression on cells infected in vitro with FV or HIV.
Highlights
In vitro. mRNA from infected and non-infected cells was isolated for real time PCR quantification of the IFNα mRNA expression
Spleen cells were isolated from naїve wild type mice or from naïve IFNAR1-/- mice and cultivated with F-MuLV infected Mus Dunni cells to infect mouse cells in vitro
Multi-parameter flow cytometry was used to determine the expression of PD-L1 on the sur-face of gp70+Ter119+, gp70+CD19+, and gp70+Gr-1+ cells isolated from spleens of 6 day FV infected WT and IFNAR1-/- mice
Summary
MRNA from infected and non-infected cells was isolated for real time PCR quantification of the IFNα mRNA expression. The numbers of IFNα mRNA copies in relation to 105 copies of mRNA for β-actin is shown. Spleen cells were isolated from naїve wild type mice or from naïve IFNAR1-/- mice and cultivated with F-MuLV infected Mus Dunni cells to infect mouse cells in vitro.
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