Leishmania major: secreted antigens of Leishmania major promastigotes shift the immune response of the C57BL/6 mice toward Th2 in vitro

Exp Parasitol. 2011 Jan;127(1):46-51. doi: 10.1016/j.exppara.2010.06.033. Epub 2010 Jul 21.

Abstract

BALB/c mice are sensitive to Leishmaniamajor infection, while C57BL/6 mice are resistant and able to mount an effective immune response against the parasite. Since the secreted antigens of L. major suppress the proliferation of BALB/c mice lymphocytes in vitro, we analyzed their effects on the immune system of resistant C57BL/6 mice. Secreted antigens were semi-purified and two fractions with immunosuppressive activity were isolated. 15 μg/ml of fraction could suppress 60% of lymphocyte proliferation and prevent the stimulated lymphocytes entering from G1 phase into the S phase of the cell cycle. These fractions decreased the production of IFN-γ, increased IL-4 level in the lymphocyte culture and down-regulated the nitric oxide production by activated macrophages. These results may suggest that L. major parasite by secreting immunosuppressive factors could down-regulate the immune system of both sensitive and resistant mice for own survival advantage.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Antigens, Protozoan / immunology*
  • Antigens, Protozoan / isolation & purification
  • Cell Cycle / immunology
  • Cell Proliferation
  • Cells, Cultured
  • Chromatography, Gel
  • Electrophoresis, Polyacrylamide Gel
  • Enzyme-Linked Immunosorbent Assay
  • Female
  • Flow Cytometry
  • Interferon-gamma / analysis
  • Interferon-gamma / biosynthesis
  • Interleukin-4 / analysis
  • Interleukin-4 / biosynthesis
  • Leishmania major / immunology*
  • Lymphocytes / cytology
  • Lymphocytes / immunology
  • Macrophages, Peritoneal / metabolism
  • Mice
  • Mice, Inbred C57BL
  • Nitric Oxide / analysis
  • Nitric Oxide / biosynthesis
  • Spleen / cytology
  • Spleen / immunology
  • Th2 Cells / immunology*

Substances

  • Antigens, Protozoan
  • Interleukin-4
  • Nitric Oxide
  • Interferon-gamma