Skip to main content
Advertisement
Browse Subject Areas
?

Click through the PLOS taxonomy to find articles in your field.

For more information about PLOS Subject Areas, click here.

< Back to Article

Table 1.

Randomized study groups, doses and routes of HIV-DNA and HIV-MVA vaccinations.

More »

Table 1 Expand

Fig 1.

Number of individuals screened, randomized and allocated to the three vaccination groups and withdrawn from the trial.

More »

Fig 1 Expand

Table 2.

Baseline characteristics.

More »

Table 2 Expand

Fig 2.

Proportion and number of participants with (A) local and (B) systemic solicited adverse events post HIV-DNA and HIV-MVA by randomization arm.

More »

Fig 2 Expand

Table 3.

Numbers and percent of non-solicited clinical adverse events by grade and relationship to vaccination.

More »

Table 3 Expand

Table 4.

Proportion of ELISpot responders to Gag and/or Env peptides two weeks post first and second HIV-MVA vaccination in each of the HIV-DNA primed groups.

More »

Table 4 Expand

Fig 3.

Magnitude of IFN-γ ELISpot responses.

The magnitude of IFN-γ ELISpot responses to (A) Gag and (B) Env two weeks after the first HIV-MVA vaccination and to (C) Gag and (D) Env two weeks after the second HIV-MVA vaccination. Data is shown for each of the HIV-DNA primed groups. ELISpot responses were considered positive if the number of SFC was >55 spots/million PBMCs and 4 times the background value. The dashed line is at a cut-off of 55 SFC/million PBMCs. Responders are shown by filled circles and non-responders are shown by open circles.

More »

Fig 3 Expand

Table 5.

Magnitude of ELISpot responses measured as SFC/106 PBMCs 2 weeks after the first and second HIV-MVA vaccination in each of the HIV-DNA primed groups.

More »

Table 5 Expand

Fig 4.

Magnitude of HIV-specific IFN-γ/IL-2 T cell responses.

The magnitude of HIV-specific IFN-γ/IL-2 T cell responses in responders as assessed by 4-colour ICS two weeks after the first (upper panel) and second (lower panel) HIV-MVA vaccination presented as Gag reactivity of CD4+ T cells (panels A and E) and of CD8+ T cells (panels B and F), and Env reactivity of CD4+ T cells (panels C and G) and of CD8+ T cells (panels D and H). The Gag-reactivity represents reactivity to either the MVA-CMDR-specific peptide pools or the HIV-DNA-specific peptide pool. A Gag HIV-DNA-specific peptide pool response is only given when the Gag MVA-CMDR-specific peptide pool response is negative. Gag-HIV-DNA-specific responses are given by triangles, while Gag and Env-HIV-CMDR-specific responses are given by circles.

More »

Fig 4 Expand

Table 6.

The proportion of ICS responders to Gag or Env peptide pools two weeks after the first and second HIV-MVA vaccination in each of the HIV-DNA primed groups.

More »

Table 6 Expand

Fig 5.

Antibody endpoint titers.

Antibody endpoint titers to native HIV-1IIIB subtype B gp160 one month after the second HIV-MVA vaccination. Data is shown for each of the HIV-DNA priming groups. The dashed line shows a titer of 100, corresponding to a 1:100 serum dilution, the lowest dilution used in the assay.

More »

Fig 5 Expand