The effects of increased heme oxygenase-1 on the lymphoproliferative response in dogs with visceral leishmaniasis

Canine visceral leishmaniasis (CVL) is known to affect the cellular immunity of infected dogs, through impairing lymphoproliferation and microbicidal mechanisms. This study examined heme oxygenase-1 (HO-1) and its metabolites, oxidative stress and IL-10 levels in CVL and investigated correlations be...

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Detalles Bibliográficos
Autores: Almeida, Breno Fernando Martins de [UNESP], Silva, Kathlenn Liezbeth Oliveira [UNESP], Chiku, Vanessa Marim [UNESP], Leal, Aline Aparecida Correa [UNESP], Venturin, Gabriela Lovizutto [UNESP], Narciso, Luis Gustavo [UNESP], Fink, Maria Fernanda Cereijido Bersni [UNESP], Eugênio, Flavia de Rezende [UNESP], Santos, Paulo Sergio Patto dos [UNESP], Ciarlini, Paulo Cesar [UNESP], Lima, Valéria Marçal Felix de [UNESP]
Tipo de recurso: artículo
Estado:Versión publicada
Fecha de publicación:2017
País:Brasil
Institución:Universidade Estadual Paulista (UNESP)
Repositorio:Repositório Institucional da UNESP
Idioma:inglés
OAI Identifier:oai:repositorio.unesp.br:11449/174042
Acceso en línea:http://dx.doi.org/10.1016/j.imbio.2016.12.006
http://hdl.handle.net/11449/174042
Access Level:acceso abierto
Palabra clave:Canine
HSP32
Leishmania infantum
Lymphoproliferation
Descripción
Sumario:Canine visceral leishmaniasis (CVL) is known to affect the cellular immunity of infected dogs, through impairing lymphoproliferation and microbicidal mechanisms. This study examined heme oxygenase-1 (HO-1) and its metabolites, oxidative stress and IL-10 levels in CVL and investigated correlations between these parameters. Additionally, the effects of HO-1 inhibition on the lymphoproliferative response and cytokine production in lymph node cells (LNCs) from infected dogs were evaluated. Forty-four dogs, 24 controls and 20 dogs with CVL were selected. Plasma and splenic levels of HO-1, haptoglobin, soluble CD163 receptor, ferritin and IL-10 were determined using capture ELISA. The HO-1 levels and relative gene expression in peripheral blood and bone marrow mononuclear cells were also determined. LNCs proliferation was evaluated with an HO-1 activator and with an HO-1 inhibitor, in the presence of the Leishmania infantum soluble antigen (SAgL), using flow cytometry. HO-1, IL-2, IFN-gamma and IL-10 were also determined in these cultures using capture ELISA. Infected dogs presented oxidative stress and increased HO-1 levels and relative gene expression, with correlation between oxidative stress and HO-1. The substances from heme metabolism and IL-10 were also elevated in the plasma and spleens of infected dogs. IL-10 and HO-1 levels were positively correlated with one another. Inhibition of HO-1 increased LNCs proliferation and decreased IL-10 and IL-2 production in the presence of SAgL. The increased HO-1 metabolism observed in CVL is probably associated with oxidative stress and increased IL-10, which could be one of the mechanisms responsible for inhibition of the lymphoproliferative response in sick dogs.