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DOI 10.1016/j.vetimm.2004.08.010

Медицинская библиотека · Veterinary immunology and immunopathology · 2005

Semi-quantitative analysis of cytokine expression in asymptomatic canine leishmaniasis.

Chamizo Cristina, Moreno Javier, Alvar Jorge

СтатьяПоддержка исследования: вне правительства СШАПеревод пока не подготовлен

Аннотация

The dog is the main reservoir of Leishmania infantum, the parasite responsible for visceral leishmaniasis in Mediterranean countries. The infection in dogs shows different clinical presentations, from subclinical/asymptomatic to a fully developed disease, depending on the host's immune responses. The Th1/Th2 dichotomy is not clear in the different forms of canine leishmaniasis, since the data available from studies of immunity response in canine leishmaniasis are scarce and fragmented. The present work describes the cytokine expression in peripheral blood mononuclear cells (PBMC) obtained from asymptomatic dogs experimentally infected with L. infantum that present a cellular protective immune response. The results obtained from freshly isolated PBMC showed expressions of TNF-alpha, IL-2, IFN-gamma, IL-10 and IL-18 mRNA, similar to those from non-infected dogs. However, there was almost no expression of IL-4 mRNA detected in the asymptomatic infected dogs compared to the control dogs. Unspecific stimulation with ConA promoted the expression in a greater or lower degree of all the cytokines studied. In vitro stimulation of PBMC with soluble leishmanial antigen (SLA) promoted the expression of IL-2, IFN-gamma, TNF-alpha, IL-18, IL-4, IL-6 and IL-10 mRNA, with the two first being specifically induced. Although both Th1 and Th2 cytokines are produced, cell mediated immunity observed in these L. infantum-infected asymptomatic dogs depended on the preferential expression of Th1 cytokines.

Для цитирования: Chamizo Cristina, Moreno Javier, Alvar Jorge. Semi-quantitative analysis of cytokine expression in asymptomatic canine leishmaniasis.. Veterinary immunology and immunopathology. 2005. DOI: 10.1016/j.vetimm.2004.08.010.

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