Schistosoma mansoni PIII antigen modulates in vitro granuloma formation by regulating CD28, CTLA-4, and CD86

C S Zouain1, P L Falcão, T S Goes

  • 1Departamento de Bioquímica e Imunologia, Instituto de Ciências Biológicas, Universidade Federal de Minas Gerais, Caixa Postal 486, CEP 31.270-901, Belo Horizonte, Brazil.

Immunology Letters
|March 17, 2004
PubMed

Insights

The study reveals that Schistosoma mansoni antigen PIII suppresses immune responses in chronic schistosomiasis patients by altering T-cell markers and cytokine production, offering insights into granuloma formation.

Area of Science:

  • Immunology
  • Parasitology
  • Cell Biology

Background:

  • Chronic schistosomiasis involves complex immune responses, including granuloma formation, which can be modulated by parasite antigens.
  • Understanding the immunoregulatory mechanisms in schistosomiasis is crucial for developing effective treatments.

Purpose of the Study:

  • To investigate the phenotypic changes in peripheral blood mononuclear cells (PBMC) from chronic schistosomiasis patients upon in vitro stimulation with Schistosoma mansoni antigen PIII.
  • To elucidate the role of PIII in modulating immune cell surface markers and cytokine profiles related to granuloma formation.

Main Methods:

  • Peripheral blood mononuclear cells (PBMC) from intestinal chronic schistosomiasis patients were stimulated with PIII antigen in an in vitro granuloma assay.
  • Flow cytometry was used to analyze the expression of surface markers CD28, CTLA-4, and CD86 on lymphocytes and monocytes.
  • Interferon-gamma (IFN-gamma) and Interleukin-10 (IL-10) levels were measured.

Main Results:

  • PIII antigen significantly decreased cellular proliferation and granuloma reaction.
  • PIII reduced IFN-gamma levels and increased IL-10 production.
  • A decrease in CD28+ T-cells and an increase in CTLA-4 and CD86 expressing cells were observed, indicating immune suppression.

Conclusions:

  • PIII modulates the in vitro granuloma reaction in schistosomiasis patients.
  • The observed immunomodulation is linked to changes in IL-10, IFN-gamma, and surface markers (CD28, CTLA-4, CD86).
  • These findings provide new insights into the immunoregulation of granulomatous hypersensitivity in human schistosomiasis.

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