3C). When analyzing the expression of CD137 in CD4+ T cells, mice vaccinated

with 10 μg mice showed a reduced expression, which diminished even more after these cells were re-stimulated in vitro with 10 μg LPG ( Fig. 3D). Together these data show that L. mexicana LPG negatively regulates CD8+ cell activation by enhancing PD-1 expression and concomitantly reducing CD137 expressions, where the degree of the modulation depends upon the dose of LPG used for immunization as well as the dose of the subsequent stimulus. In contrast to CD8+ T cells, vaccination with find more LPG had no inhibitory effect on CD4+ T cells, since it did not modify their PD-1 expression and re-stimulation with LPG reduced their PD-1 expression. Thus, LPG vaccination selleck chemical seems to exert the inhibitory effect only on CD8+ T cells, in a dose dependent fashion. To analyze whether parasite infection modulates PD-1 expression

in T lymphocytes, BALB/c mice were infected in the earlobe dermis with 1 × 104 or 1 × 105L. mexicana promastigotes. Mice were sacrificed prior to ulceration of the lesions. Splenocytes were isolated and re-stimulated in vitro with 1, 5 or 10 μg LPG during 24 h and PD-1 as well as CD137 were analyzed. We found that PD-1 expression is enhanced in CD8+ T cells of mice infected with 1 × 104 (0.5-fold) or 1 × 105 (3.6-fold) parasites, as compared to CD8+ T cells from non-infected mice ( Fig. 4A). In vitro stimulation with all three doses of LPG showed the same high expression of PD-1. The analysis of CD137 in CD8 T cells showed a 40% down-regulation in mice infected with 1 × 104 promastigotes, whereas mice infected with 1 × 105 promastigotes showed a similar expression as non-infected mice. In vitro re-stimulation with LPG did not alter CD137 expression ( Fig. 4B). CD4+ lymphocytes showed a minimal increase in PD-1 expression after infections with either number L. mexicana parasites, and showed no changes despite secondary stimuli with LPG ( Fig. 4C). Furthermore, Casein kinase 1 the expression of CD137 in CD4+ T

cells of infected mice also remained unaltered. The only up-regulation of this activation marker was observed in CD4+ T cells of mice infected with 1 × 105 Libraries parasites after they were re-stimulated in vitro with 5 μg LPG ( Fig. 4D). In conclusion these results show that L. mexicana infection induces significantly enhanced PD-1 expression only in CD8+ T cells, in a dose-dependent fashion. The reduced expression of CD137 in association with the increased levels of PD-1 in these CD8+ T cells seems to indicate that they resemble an exhausted phenotype. PD-1 is minimally expressed in CD4+ cells during L. mexicana infections and not altered by in vitro LPG stimuli, showing that L. mexicana exerts a stronger inhibitory effect on CD8+ T cells, as compared to CD4+ T cells.