dc.creatorDíaz, N. L.
dc.creatorFernández, M.
dc.creatorFigueira, E.
dc.creatorRamírez, R.
dc.creatorMonsalve, I. B.
dc.creatorTapia, Félix J.
dc.date2015-07-28T20:02:17Z
dc.date2015-07-28T20:02:17Z
dc.date2003-06
dc.date.accessioned2022-10-28T01:14:21Z
dc.date.available2022-10-28T01:14:21Z
dc.identifierhttp://hdl.handle.net/10872/11750
dc.identifier.urihttps://repositorioslatinoamericanos.uchile.cl/handle/2250/4945511
dc.descriptionWe 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.
dc.languageen
dc.publisherCLINICAL AND EXPERIMENTAL DERMATOLOGY
dc.relation;28
dc.subjectleishmaniasis
dc.subjectNitric oxide
dc.subjectcellular immunity
dc.subjectcutaneous
dc.subjectexperimental
dc.titleNitric oxide and cellular immunity in experimental cutaneous leishmaniasis
dc.typeArticle


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