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. 2018 Nov 30;13(11):e0207794. doi: 10.1371/journal.pone.0207794

Fig 3. T cell responses to αDCIR.HIV5pep and αCD40.HIV5pep vaccines in naïve Rhesus macaques.

Fig 3

PBMCs were harvested at the indicated time points and analyzed by IFNγ ELISPOT using pools of overlapping Gag Pol and Nef peptides corresponding to sequences carried by the DC-targeting vector (HIV5 peptides, shown in light grey), or pools of overlapping Gag Pol and Nef peptides corresponding to sequences not carried by the DC-targeting vaccines but carried by MVA GagPolNef (non-HIV5 pep, shown in dark grey). (A) IFNγ ELISPOT data from animals vaccinated with three administrations of 250 μg αDCIR.HIV5pep (G3) or (B) αCD40.HIV5pep (G4) plus 1 mg poly-ICLC followed by a boost with MVA GagPolNef. Responses from individual animals in the indicated groups are shown as points and were summed for these two pool sets. The mid-line of the box denotes the median, and the ends of the box denote the 25th and 75th percentiles. The whiskers are the minimum/maximum value higher/lower than 1.5* Inter-Quartile Interval. Values after the second and third αDCIR.HIV5pep vaccinations at week 0 compared to weeks 6 or 14 were not significantly different (G3; ns; respectively, p = 0.03, p = 0.1). Values after the second and third αCD40.HIV5pep vaccinations at week 0 compared to weeks 6 or 14 were not significantly different (G4; *; respectively, p = 0.15, p = 0.03). (C) and (D) IFNγ ELISPOT data for individual Gag, Pol and Nef peptides stimulations as described above. The X-axis shows sampling time in weeks. S6 Table and S3 Table and S1 File show data corresponding to this figure.