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PLoS One ; 8(10): e73873, 2013.
Artigo em Inglês | MEDLINE | ID: mdl-24146743

RESUMO

Leishmania infantum infection in humans and dogs can evolve with a wide range of clinical presentations, varying from asymptomatic infections to visceral leishmaniasis. We hypothesized that the immune response elicited by L. infantum infection could modulate whether the host will remain asymptomatic or progress to disease. A total of 44 dogs naturally infected with L. infantum were studied. Leishmania burden was estimated in the blood and spleen by qPCR. The expression of IFN-γ, TNF-α, IL-10 and Iron Regulatory Protein 2 (IRP2) were determined in the spleen by quantitative PCR. Sera cytokines were evaluated by ELISA. Dogs were grouped in quartiles according parasite burden. Increased expression of IFN-γ and TNF-α was associated with reduced Leishmania burden, whereas increased IL-10 and IRP2 expressions were associated with higher Leishmania load. Increased plasma albumin and IFN-γ expression explained 22.8% of the decrease in parasite burden in the spleen. These data confirm that lower IFN-γ response and higher IL-10 correlated with increased parasite load and severity of the visceral leishmaniasis in dogs. The balance between the branches of immune response and the intracellular iron availability could determine, in part, the course of Leishmania infection.


Assuntos
Doenças do Cão/genética , Interferon gama/imunologia , Interleucina-10/imunologia , Proteína 2 Reguladora do Ferro/imunologia , Leishmania infantum/imunologia , Leishmaniose Visceral/veterinária , Animais , Doenças do Cão/imunologia , Doenças do Cão/parasitologia , Cães , Feminino , Expressão Gênica , Interações Hospedeiro-Parasita , Interferon gama/genética , Interleucina-10/genética , Ferro/imunologia , Ferro/metabolismo , Proteína 2 Reguladora do Ferro/genética , Leishmania infantum/patogenicidade , Leishmaniose Visceral/genética , Leishmaniose Visceral/imunologia , Leishmaniose Visceral/parasitologia , Masculino , Carga Parasitária , Albumina Sérica/imunologia , Albumina Sérica/metabolismo , Índice de Gravidade de Doença , Baço/imunologia , Baço/parasitologia , Baço/patologia , Fator de Necrose Tumoral alfa/genética , Fator de Necrose Tumoral alfa/imunologia
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