To assess the role of bacterial and viral stimuli in Th2 differentiation, CD4+ T cells from cord blood were assayed in an MLR together with different strains of bacteria and virus. To compare the effect of the different microbes on cytokine secretion, we assessed the relative change in cytokine production for each microbe. The relative change was calculated using the amount of cytokine produced in MLR cultures containing a specific microbe, divided by the cytokine amount secreted in an MLR lacking microbe. All enveloped viruses tested (coronavirus, CMV, HSV-1, influenza virus and morbillivirus)

downregulated the IL-13 responses in cord blood cocultures (Fig. 3E,F). The non-enveloped AP24534 in vitro viruses, adenovirus and poliovirus had no effect on the IL-13 production in cord MLR cultures using either pDC (Fig. 3F) or mDC (Fig. 3E) from cord blood as antigen presenting cells. Neither did any of the bacteria reduce the IL-13 responses. Instead, S. aureus stimulated pDC increased the IL-13 production in responding CD4+ cord T cells (Fig. 4F). We were not able to document any significant inhibitory effects on the IL-5 production by the virus, most likely due to the very low initial production selleck screening library of this

cytokine (not shown). The effect of viral and bacterial stimuli on Th1 cytokine secretion was assessed using cord CD4+ T cells cocultured with allogenic pDC or mDC from cord blood. Both bacteria and virus could affect IL-2 and IFN-γ secretion by cord CD4+ T cells (Figs 3 and 4). Influenza virus was the most Terminal deoxynucleotidyl transferase efficient inducer of IL-2 and significantly enhanced the responses in cord CD4+ T cells exposed to cord pDC (Fig. 3B) and to cord mDC (Fig. 3A). Influenza virus also enhanced the IFN-γ responses, but only in cord T cell/mDC cultures (Fig. 3C). None of the other viruses tested affected the IL-2 or IFN-γ production in these cocultures except CMV that reduced the IL-2 production from cord CD4+ T cells and pDC cocultures (Fig. 3B), that is from the

cells with the highest initial IL-2 production (Fig. 2A). Staphlococcus aureus was the only bacteria that enhanced IL-2 responses by cord CD4+ T cells exposed to both mDC (Fig. 4A) and pDC (Fig. 4B). Staphlococcus aureus was also a potent inducer of IFN-γ responses in both pDC and mDC stimulated cord CD4+ T cells (Fig. 4C,D). To assess innate cytokine secretion in cord DC, pDC and mDC from cord blood were stimulated with different strains of bacteria and virus together with allogenic cord CD4+ T cells. We found that all Gram-positive bacteria, but not E. coli or any of the viruses, promoted an IL-12 p40 response in MLR cultures with mDC (Fig. 5A,C) but not with pDC (not shown). The increase in IL-12 production in C. difficile stimulated cell cultures was, however, not statistically significant, even though there was a strong trend (Fig. 5A). We also analysed the ability of virus and bacteria in evoking an IFN-α response in pDC.