We evaluated the effect of immunosuppressive therapy on the course of infec
tion, the spleen cell immunophenotype and cytokine production during murine
Leishmania infantum visceral leishmaniosis (VL), Rousseau et al, [1] recen
tly reported that prolonged administration of dexamethasone induces limited
reactivation of chronic murine visceral leishmaniosis, with no clear Th1-T
h2 cytokine patterns. We found that another glucocorticoid, hydrocortisone
acetate, had similar effects during acute visceral leishmaniosis, i.e. an i
ncrease in parasite burden in the spleen, but not the liver, of infected mi
ce. A significant increase in parasite burden in both the liver and the spl
een was only achieved when mice were treated with combined dexamethasone pentoxifylline immunotherapy; increases in parasite burden were never assoc
iated,vith a specific spleen cell immunophenotype or a Th1-Th2 cytokine sec
retion profile.