1A, upper right quadrant). Interestingly, there was considerable heterogeneity in CD11c staining within the Y-Ae+ population (Fig. 1B) with several different populations with different levels of Y-Ae staining or CD11c expression clearly evident. In this experiment, approximately 50% of CD11chigh cells from EαGFP-immunised mice were Y-Ae+ (Fig. 1B, upper panel, upper right quadrant), however, there were a smaller percentage (∼28%; ∼0.6% of live cells) with a Y-Ae+CD11clow/− phenotype (Fig. 1B, upper panel, upper left quadrant). At present we have not attempted to further characterise these Y-Ae+CD11clow/− cells. EαGFP Ag was demonstrated at both

the injection site (Fig. 1C) and in the local draining lymph nodes (Fig. 1D and E) 30 min after injection. EαGFP appeared to flow from one side of the lymph node, from the subcapsular sinus into the paracortical areas (Fig. 1E) as has been observed previously for other protein Ags, including EαRFP [1]. this website To maximise the sensitivity of Ag detection in lymphoid tissues, we used GFP-specific

rabbit IgG to amplify the GFP signal (Fig. 1F). At 24 h we observed that large areas of the draining lymph nodes were Y-Ae+ (Fig. 1G) as has been reported previously [1]. B cell follicular areas were not stained with Y-Ae, with the majority of Y-Ae+ cells being Selleck Anti-cancer Compound Library found in the interfollicular areas, paracortex and subcapsular sinus. As was observed by flow cytometry, Y-Ae staining co-localised with CD11c+ cells (Fig. 1H, yellow), however there were some Y-Ae+CD11clow/− cells (red). The maximum amount of Ag detected following DNA vaccination is known to be in the nanogram range in muscle and serum [10] and [16], however the amount of Ag that reaches lymphoid tissues is

unknown. Estimates are that fewer than 2% of all CD11c+ cells may contain plasmid-encoded Ag following transdermal gene gun delivery [17] and it is not known how many of these 17-DMAG (Alvespimycin) HCl cells present Ag to naïve lymphocytes. Therefore we wished to establish sensitive methodologies to study those cells that acquire and present DNA-encoded Ag, particularly in lymphoid tissue. To determine the minimum amount of protein Ag that could be detected in vivo and how much Ag is needed to be able to detect cells displaying pMHC complexes, we administered a range of doses of EαGFP protein and examined the draining lymph nodes for cell-associated Ag and cells displaying pMHC complexes. The aim of this protein injection study was to demonstrate the sensitivity of the assay systems in a widely studied situation such as subcutaneous injection. Both Ag distribution and the proportion of GFP+ cells were influenced by Ag dose (Fig. 2A and B). GFP+ cells were detected in the CLNs (Fig. 2A and B), BLNs and ILNs (data not shown), 24 h after injection of 100 μg Ag (n = 3, p < 0.05). However, lower Ag doses yielded far fewer GFP+ within both the CD11c+ ( Fig. 2A) and CD11clow/− ( Fig. 2B) populations.