Abstract

BackgroundThere is limited information available on cytokine profiles in dogs with different degrees of disease severity due to natural infection of Leishmania infantum. The aim of this study was to investigate L. infantum-specific IFN-γ and IL-10 production in blood from dogs with leishmaniosis at diagnosis and correlate these findings with disease severity, humoral immune response and blood parasitemia.MethodsSixty dogs were diagnosed based on physical examination, routine laboratory tests, L. infantum-specific antibody levels measured by quantitative ELISA and blood parasitemia by real-time PCR. Heparin whole blood was stimulated with L. infantum soluble antigen (LSA) and concanavalin A (ConA) and incubated for 5 days. IFN-γ and IL-10 concentrations were measured in supernatants with sandwich ELISAs.ResultsThe majority of dogs (n = 36) were classified as LeishVet stage II (moderate disease). The rest of the dogs were classified as stage I (n = 10), III (n = 10) and IV (n = 4). Dogs classified with stage I and IIa presented significantly higher (P = 0.02) LSA IFN-γ concentrations, lower (P <0.0001) antibody levels and a tendency for lower blood parasitemia (P = 0.1) than dogs classified with stages IIb, III or IV while no differences in ConA IFN-γ or IL-10 concentrations were observed among groups. Thirty-five dogs produced significantly higher LSA IFN-γ (mean ± SD: 2320 ± 3960 pg/ml) and ConA IFN-γ (mean ± SD: 7887 ± 7273 pg/ml) when compared with 25 dogs that did not produce detectable LSA IFN-γ but produced ConA IFN-γ (mean ± SD: 4917 ± 5233 pg/ml). IFN-γ producer dogs presented lower (mean ± SD: 5750 ± 14,082 ELISA units (EU), P = 0.001) antibody levels and blood parasitemia (mean ± SD: 5 ± 10 parasites/ml, P = 0.001) when compared with IFN-γ non-producers (mean ± SD: 19,638 ± 28,596 EU and 1100 ± 5112 parasites/ml), respectively. LSA IL-10 was not detectable in 34 dogs while 49 dogs secreted ConA IL-10 (mean ± SD of 90 ± 103 pg/ml). LSA IFN-γ concentration was negatively correlated with blood parasitemia and antibody levels and positively correlated with ConA IFN-γ and LSA IL-10 concentrations.ConclusionsThe results of this study demonstrate that sick dogs lacking L. infantum specific IFN-γ production in stimulated whole blood produce a strong humoral response, have a high blood parasitemia and severe clinical disease. IL-10 does not appear to be a marker of disease severity.

Highlights

  • There is limited information available on cytokine profiles in dogs with different degrees of disease severity due to natural infection of Leishmania infantum

  • Description of clinical data of dogs, clinical staging and specific L. infantum IFN-γ response classifications Both sexes were represented by 25 females and 35 males

  • Dogs classified with stage I and IIa group presented significantly higher (Mann-Whitney U-test: Z = -2.32, P = 0.02) L. infantum soluble antigen (LSA) IFN-γ concentrations than dogs classified with stages IIb, III or IV group while no differences in concanavalin A (ConA) IFN-γ concentrations were observed among these two groups

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Summary

Introduction

There is limited information available on cytokine profiles in dogs with different degrees of disease severity due to natural infection of Leishmania infantum. The aim of this study was to investigate L. infantum-specific IFN-γ and IL-10 production in blood from dogs with leishmaniosis at diagnosis and correlate these findings with disease severity, humoral immune response and blood parasitemia. Other Leishmania species have been reported to infect dogs such as L. major [1], L. tropica and L. braziliensis [2,3,4], Leishmania infantum is the most common species in the Mediterranean basin [5, 6]. Dogs are considered the principal reservoir for leishmaniosis in people due to L. infantum in the Mediterranean basin, Middle East and South America [5]. Both innate and adaptive immune responses play a role in the outcome of Leishmania infection. Th1 secrete interleukin-2 (IL-2), TNF-alpha and interferongamma (IFN-γ) and this response is associated with controlling infection while Th2 cells secrete interleukin-4 (IL-4), interleukin-5 (IL-5), interleukin-10 (IL-10), and transformation growth factor beta (TGF-β) and correlate with disease progression [7, 8]

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