50 μg/ml of anti-H-2Kd competitive binding antibody (BD PharMigen, San Diego, USA) was added to each well to prevent dissociated tetramer from re-binding and plates were incubated at 37 °C, 5% CO2. At each time point, cells were transferred into ice-cold FACS selleck chemicals buffer to stop the reaction, washed and resuspended in 100 μl of FACS buffer containing 0.5% paraformaldehyde. 100,000 events were acquired on a FACs Calibur flow cytometer (Becton-Dickinson, San Diego, USA) and analysed using Cell Quest Pro software.

In tetramer dissociation assays, lower dissociation rates or stronger MHC-I/peptide complex binding to the TCR complex of CD8 T cell, is associated with higher avidity [43]. IFN-γ or IL-2 capture ELISpot assays was used to assess IFN-γ or IL-2 HIV-specific T cell responses [40]. Briefly, 2 × 105 spleen or GN cells were added to 96-well Millipore PVDF

plates (Millipore, selleck MA, Ireland) coated with 5 μg/ml of mouse anti-IFN-γ or IL-2 capture antibodies (BD PharMigen, San Diego, CA), and stimulated for 12 h or 22 h respectively for IL-2 or IFN-γ ELISpot, in the presence of H-2Kd immuno-dominant CD8+ T cell epitope, Gag197–205 AMQMLKETI (synthesised at the Bio-Molecular Resource Facility at JCSMR). ConA-stimulated cells (Sigma, USA) were used as positive controls and unstimulated cells as negative controls. For both ELISpot assays, all steps were carried out exactly as described previously [20] and [40]. The graphed data are expressed as SFU (spot-forming units) per 106 T cells and represent mean values ± SD. Unstimulated cell counts were subtracted from each stimulated value before plotting the data. In all assays the background SFU counts were between 4–10 SFU for IFN-γ and 5–18 SFU for IL-2 ELISpot. Also the unimmunised animals did not show any responses following Gag197–205-AMQMLKETI stimulation. IFN-γ and TNF-α producing HIV-specific CD8 T cells, were analysed as described in Ranasinghe

et al. [20] and [40]. Briefly, 2 × 106 lymphocytes were stimulated with AMQMLKETI peptide at 37 °C for 16 h, and further incubated with Brefeldin A (eBioscience, CA, USA) for 4 h. Cells were surface-stained with CD8-Allophycocyanin (Biolegend, USA) then fixed and permeabilized prior to intracellular staining with IFN-γ-FITC and TNF-α-PE (Biolegend, USA). Total 100,000 gated events per sample were collected using FACS Calibur flow Mannose-binding protein-associated serine protease cytometer (Becton Dickinson, San Diego, CA), and results were analysed using Cell Quest Pro software. Prior to plotting the graphs the unstimulated background values were subtracted from the data, The IFN-γ+ cell counts were less than 0.05–0.1% in unimmunised or unstimulated samples similar to our previous studies [23]. Female BALB/c mice n = 8 were i.n./i.m. prime-boost immunised using the strategies 1, 4 and 5 indicated in Table 1. ELISA was used to determine HIV-1 p55 gag-specific IgG1 and IgG2a serum antibody titres similar to as described in Ranasinghe et al. [40].