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Toxoplasma gondii: the role of IFN-gamma, TNFRp55 and iNOS in inflammatory changes during infection.

Abstract
In order to examine the role of IFN-gamma, TNFRp55 and iNOS in inflammatory reaction during toxoplasmosis, IFN-gamma(-/-), TNFRp55(-/-) and iNOS(-/-) mice were experimentally infected with Toxoplasma gondii ME-49 strain. The organs of the mice were evaluated for histology and immunohistochemistry in detection of tissue parasitism and iNOS positive cells. IFN-gamma(-/-) mice presented mild inflammation in peripheral organs associated with a high parasitism and mortality in the acute phase of infection. In contrast, the peripheral organs of WT, TNFRp55(-/-) and iNOS(-/-) mice, presented a significant inflammatory reaction and low tissue parasitism in the same period of infection. The inflammatory lesions and tissue parasitism were increased and more severe in the Central Nervous System (CNS) of TNFRp55(-/-) and iNOS(-/-) with a progression of infection, when compared to WT mice. In these knockout animals, the inflammatory changes were associated with low levels or no expression of iNOS in TNFRp55(-/-) and iNOS(-/-) mice, respectively.
AuthorsNeide Maria Silva, Júlio César Menezes Vieira, Claudia Martins Carneiro, Wagner Luiz Tafuri
JournalExperimental parasitology (Exp Parasitol) Vol. 123 Issue 1 Pg. 65-72 (Sep 2009) ISSN: 1090-2449 [Electronic] United States
PMID19501090 (Publication Type: Comparative Study, Journal Article, Research Support, Non-U.S. Gov't)
Chemical References
  • Receptors, Tumor Necrosis Factor, Type I
  • Tumor Necrosis Factor Decoy Receptors
  • recombinant human tumor necrosis factor-binding protein-1
  • Interferon-gamma
  • Nitric Oxide Synthase Type II
Topics
  • Animals
  • Brain (parasitology)
  • Heart (parasitology)
  • Immunohistochemistry
  • Inflammation (immunology)
  • Interferon-gamma (physiology)
  • Liver (parasitology)
  • Lung (parasitology)
  • Mice
  • Mice, Inbred C57BL
  • Mice, Knockout
  • Nitric Oxide Synthase Type II (physiology)
  • Receptors, Tumor Necrosis Factor, Type I (physiology)
  • Spinal Cord (parasitology)
  • Spleen (parasitology)
  • Toxoplasma (physiology)
  • Toxoplasmosis, Animal (immunology, pathology)
  • Tumor Necrosis Factor Decoy Receptors (physiology)

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