A cytokine network balance influences the fate ofLeishmania (Viannia) braziliensisinfection in a cutaneous leishmaniasis hamster model

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Abstract

The golden hamster is a suitable model for studying cutaneous leishmaniasis (CL) due to Leishmania (Viannia) braziliensis . Immunopathological mechanismsare wellstablished inthe L. (L.) major-mouse model, in which IL-4 instructs a Th2 response towards progressive infection. In the present study, we evaluatedthe natural history of L. braziliensis infection from its first stagesup to lesion establishment, with the aim ofidentifyingimmunological parameters associated with the disease outcome and parasitismfate. To this end, hamsters infected with 10 4 , 10 5 ,or 10 6 promastigoteswere monitored duringthe first hours (4h, 24h), early (15, 30 days) and late (50 days) post-infection (pi) phases. Cytokines, iNOS and arginasegene expression were quantified in the established lesions by RT-PCR. Compared to the 10 5 or 10 6 groups, 10 4 animals presented lower lesions sizes, less tissue damage,and lower IgG levels. Basal gene expression in normal skin was high for TGF-β, and intermediary for TNF, IL-6, and IL-4.At 4hpi, no cytokine induction was observed in the 10 4 group, while an upregulation of IL-6, IL-10, and IL-4 was observed in the 10 6 group. At 15dpi, lesion appearance was accompanied byan increasedexpression of all assessed cytokines, markedly in the 10 5 and 10 6 groups. Upregulation of all investigated cytokines was observed in the late phase, although less expressive in the 10 4 group. IFN-γ was the depending variable influencing tissue damage, while IL-6 was associatedto parasite load. The network correlating gene expression and clinical and laboratorial parameters indicated inoculum-independent associations at 15 and 30dpi.A strong positive network correlation was observed in the 10 4 group, but not in the10 5 or 10 6 groups. In conclusion, IL-4, IL-6, IL-10, and TGF-β are linkedto L. braziliensisprogression . However, a balanced cytokine network is the key for an immune response able to reduce the ongoing infection and reduce pathological damage.

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last seen: 2026-05-19T01:45:01.086888+00:00