Comparative study of the in situ immune response in oral and nasal mucosal leishmaniasis

Parasite Immunol. 2012 Jan;34(1):23-31. doi: 10.1111/j.1365-3024.2011.01343.x.

Abstract

Mucosal Leishmaniasis (ML) may occur in both nasal and oral mucosa. However, despite the impressive tissue destruction, little is known about the oral involvement. To compare some changes underlying inflammation in oral and nasal ML, we performed immunohistochemistry on mucosal tissue of 20 patients with ML (nasal [n = 12]; oral [n = 8] lesions) and 20 healthy donors using antibodies that recognize inflammatory markers (CD3, CD4, CD8, CD22, CD68, neutrophil elastase, CD1a, CLA, Ki67, Bcl-2, NOS2, CD62E, Fas and FasL). A significantly larger number of cells, mainly T cells and macrophages, were observed in lesions than in healthy tissue. In addition, high nitric oxide synthase 2 (NOS2) expression was associated with a reduced detection of parasites, highlighting the importance of NOS2 for parasite elimination. Oral lesions had higher numbers of neutrophils, parasites, proliferating cells and NOS2 than nasal lesions. These findings, together with the shorter duration of oral lesions and more intense symptoms, suggest a more recent inflammatory process. It could be explained by lesion-induced oral cavity changes that lead to eating difficulties and social stigma. In addition, the frequent poor tooth conservation and gingival inflammation tend to amplify tissue destruction and symptoms and may impair and confuse the correct diagnosis, thus delaying the onset of specific treatment.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Aged
  • Aged, 80 and over
  • Female
  • Humans
  • Immunohistochemistry
  • Immunologic Factors / analysis
  • Inflammation / immunology
  • Inflammation / pathology
  • Leishmaniasis / immunology*
  • Leishmaniasis / pathology*
  • Macrophages / immunology
  • Male
  • Microscopy
  • Middle Aged
  • Mouth Mucosa / immunology*
  • Mouth Mucosa / pathology*
  • Nasal Mucosa / immunology*
  • Nasal Mucosa / pathology*
  • T-Lymphocytes / immunology

Substances

  • Immunologic Factors