Variation of cytokine patterns related to therapeutic response in diffuse cutaneous leishmaniasis

G Bomfim1, C Nascimento, J Costa

  • 1Serviço de Imunologia (HUPES-FAMED), Universidade Federal da Bahia, Brazil.

Experimental Parasitology
|November 1, 1996
PubMed

Insights

Diffuse cutaneous leishmaniasis patients show altered cytokine profiles, with low interferon-gamma (IFN-γ) during active disease and transient increases post-treatment. This immune response is insufficient to prevent disease relapse.

Area of Science:

  • Immunology
  • Parasitology
  • Dermatology

Background:

  • Diffuse cutaneous leishmaniasis (DCL) is a rare, disseminated form of leishmaniasis.
  • DCL is characterized by cutaneous nodules and anergy to leishmanial antigens.
  • Previous studies noted low IFN-γ in DCL skin lesions during active disease.

Purpose of the Study:

  • To investigate cytokine mRNA expression patterns in DCL patients.
  • To correlate cytokine profiles with disease stages and treatment response.
  • To explore immune factors contributing to DCL pathogenesis and relapse.

Main Methods:

  • Analysis of cytokine mRNA expression (IFN-γ, IL-2, IL-4, IL-10) in skin lesions and peripheral blood mononuclear cells (PBMCs).
  • Comparison of cytokine patterns during active disease, post-treatment, and clinical relapse.
  • Correlation of cytokine expression with clinical status.

Main Results:

  • Active DCL showed no IFN-γ mRNA but expressed IL-2, IL-4, and IL-10 mRNA.
  • Transient healing correlated with IFN-γ and low IL-10 mRNA expression.
  • Relapse was associated with decreased IFN-γ and absent IL-10 mRNA.

Conclusions:

  • Cytokine profiles in DCL vary significantly across disease stages.
  • IFN-γ expression correlates with clinical improvement but does not prevent relapse.
  • Other immune factors beyond Th1/Th2 balance may impair anti-Leishmania responses in DCL.