Please use this identifier to cite or link to this item: https://saber.ucv.ve/jspui/handle/10872/11750
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dc.contributor.authorDíaz, N. L.-
dc.contributor.authorFernández, M.-
dc.contributor.authorFigueira, E.-
dc.contributor.authorRamírez, R.-
dc.contributor.authorMonsalve, I. B.-
dc.contributor.authorTapia, Félix J.-
dc.date.accessioned2015-07-28T20:02:17Z-
dc.date.available2015-07-28T20:02:17Z-
dc.date.issued2003-06-
dc.identifier.urihttp://hdl.handle.net/10872/11750-
dc.description.abstractWe examined the local and systemic production of nitric oxide (NO) and the pattern of cytokine during the course of Leishmania mexicana infection in susceptible BALB ⁄ c and resistant C57BL ⁄ 6 mice. NO derivatives were measured in serum, and the expression of inducible nitric oxide synthase (iNOS), interferon (IFN-c), interleukin (IL-4) and epidermal Langerhans cells (LC) was measured in the lesions by immunohistology. Circulating NO concentrations, iNOS+ cell density, IFN-c+ Th1 cells and CD205+ Langerhans cells were higher in early lesions of resistant C57BL ⁄ 6 mice. In contrast, susceptible BALB ⁄ c mice developed chronic and progressive lesions with a predominance of IL-4+ Th2 cells. In both susceptible and resistant mice, lesion size and lymph node volume followed a similar course. The early local and systemic production of NO in resistant mice may be related with the premature production of IFN-c observed, contributing to the resolution of the lesion.es_VE
dc.language.isoenes_VE
dc.publisherCLINICAL AND EXPERIMENTAL DERMATOLOGYes_VE
dc.relation.ispartofseries;28-
dc.subjectleishmaniasises_VE
dc.subjectNitric oxidees_VE
dc.subjectcellular immunityes_VE
dc.subjectcutaneouses_VE
dc.subjectexperimentales_VE
dc.titleNitric oxide and cellular immunity in experimental cutaneous leishmaniasises_VE
dc.typeArticlees_VE
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