Mice that received the i.n. FPV-HIV-IL-4C118/i.m. VV-HIV-IL-4C118 vaccination showed better protective efficacy compared the previously tested IL-13Rα2 adjuvanted vaccines [23] (Fig. 7A and B). The IL-4C118 and adjuvanted group showed significantly higher (p < 0.05) recovery rates compared to the wild type BALB/c mice that received the control vaccination, specifically at peak influenza infection ( Fig. 7A). The above protective data were also consistent with the slower dissociation rates ( Fig. 1) the enhanced KdGag197–205 tetramer CD8+ T cell staining ( Fig. 2) and the polyfunctional IFN-γ/IL-2 CD8 T cell responses
observed in the systemic and mucosal compartments ( Fig. 4), following immunisation with the IL-4C118 antagonist vaccine. As shown in Gefitinib clinical trial C646 chemical structure Fig. 6, both IgG1 and IgG2a anti-Gag p55 responses were similar between mice immunised with either the control or the IL-4C118 adjuvanted vaccines. Suggesting that antibody had little influence upon the outcome of the PR8-KdGag197–205
challenge and the difference in immune protection observed was determined predominantly by the HIV-Gag specific CD8+ T cell response. We have previously demonstrated that the i.m./i.m. poxvirus vectored heterologous prime-boost vaccine strategy induces elevated numbers of HIV-specific CD8+ T cells of lower avidity expressing IL-4 and IL-13 compared to a purely mucosal vaccination [20] and [21]. These studies also demonstrated that the magnitude of HIV-specific CTLs did not correlate with the avidity measured by MHC-1/CD8 T cell interaction. Using gene knockout mice it was later established that a higher avidity HIV specific CD8+ T cell Phosphatidylinositol diacylglycerol-lyase response can be generated in the absence of IL-13, with enhanced protective efficacy following a surrogate influenza-HIV
challenge [23] and [44] These observations suggested that IL-4 and IL-13 cytokines influenced the induction and/or expansion of the CD8+ T cell population following vaccination. The current studies demonstrated that the IL-4C118 adjuvant, an antagonist for both type I/II IL-4R receptors which blocks both IL-4 and IL-13 cell signalling (see Suppl. Diagram 1), included in both the prime and booster HIV vaccine strategy (i) significantly enhanced HIV specific KdGag197–205 positive CD8+ T cell response (average 20% of total CD8+ T cells), compared to the non-adjuvant vaccine eliciting average 7% of CD8+ T cells, (ii) induced enhanced numbers of effector and memory mucosal and systemic HIV specific CD8+ T cells that expressed IFN-γ, TNF-α and IL-2 which associated with high avidity T cells of better protective efficacy following a surrogate influenza-KdGag197–205 challenge, compared to the control vaccination.
No related posts.