2b and 3a). The reason for this discrepancy is not clear but might be attributed to the nature of the stains used in both studies. In contrast to induction of Ifng mRNA, the expression of Il12 mRNA induced by the four strains in early period after the infection was negligible. The results showed consistency with the results of Reiner et al., suggesting that Leishmania spp. avoid the induction of IL-12 from the host macrophages in vitro and in vivo, during the first week post-infection. During this period, the parasites have the opportunity to survive and replicate within the macrophages [25]. However, in

parallel to the expression of Ifng mRNA, the induction of Il12 mRNA expression was observed at the late period post-infection, particularly in LN of mice infected with DA39 strain. Taken together, in addition to inducing the highest expression of Ifng mRNA at the early and late stages of the infection, DA39 strain 17-AAG manufacturer has the ability to induce another Th1 related cytokine, that is, Il12 at transcriptional level during late periods after the infection. Considering that IL-12 has a main role in initiation of a protective immune response [26] and is necessary for control of selleck chemicals the parasite in the host [25], it seems that DA39 strain has the ability to induce the lowest load of the parasite and the highest expression levels of IFN-γ and IL-12 cytokines

in LN of the infected BALB/c mice. On the SPTLC1 other hand, a burst of Il4 mRNA expression was observed in draining LN of all mice infected by the four strains at the early periods. Reports suggest that rapid expression of Il4 mRNA in draining LN of BALB/c mice infected with L. major is produced by Vβ4- Vα8CD4+ T cells [27, 28]. Our data showed that different strains of L. major induce considerable expressions of Il4 mRNA in draining LN of the susceptible mice at the beginning of the infection, but in different profiles. DA39 strain showed the highest level of expression at 16 h post-infection. The result shows consistency with the results of Launois et al. [29] who have described the peak of Il4 transcripts at 16 h post-infection.

Moreover, in the late period post-infection, all strains displayed augmented level of Il4 mRNA expression at W1 post-infection, and amongst them, DE5 strain showed the highest levels of Il4 mRNA expression, 1 week post-infection. However, the expression of Il4 transcripts induced by all strains were gradually reduced at W3 and W5 post-infection and reached to the lowest levels at W8 in LN of the mice, inoculated by all strains. Interestingly, DA39 strain showed the lowest expression of Il4 mRNA during the 3rd, 5th and 8th weeks post-infection. The reduction in Il4 mRNA at late stages of the infection shows a tendency of BALB/c mice to cure at W8 post-infection in all groups. However, it seems that the control of the infection needs a stronger Th1 cytokines expression in LN of the inoculated BALB/c mice.