Characterization of T-cell immune responses of Echinococcus multilocularis-infected C57BL/6J mice

Parasite Immunol. 1996 Sep;18(9):463-72. doi: 10.1111/j.1365-3024.1996.tb01030.x.

Abstract

Specific and non-specific parasite-induced changes in lymphocyte responses were analysed in C57/BL/6J mice after intrahepatic infection with Echinococcus multilocularis. Spleen cells harvested at selected times after infection were in vitro stimulated with mitogens or a crude soluble parasite extract (EmAg) at an optimized dose. Cell proliferative responses to Con-A were not modified by the infection over the first 22 weeks. In contrast, LPS-induced responses were decreased from the 13th week. A strong CD4+ proliferative T-cell response to the parasitic extract of infected mouse spleen cells was observed at the early stage of infection. This response then progressively decreased but remained significantly higher than that of control mice until the 19th week of infection. Cytokine production was investigated after in vitro EmAg stimulation of spleen cells. IFN-gamma, IL-2, IL-5 were produced within the first weeks after infection whereas the detection of IL-10 was slightly delayed. Thus, the promotion of the disease does not appear associated with the expansion of one rather than another T-cell subset in C57BL/6J mice. A general immunosuppression affecting both mitogenic and parasite-specific T-cell responses was observed at the end of the infection.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Antigens, Helminth / administration & dosage
  • B-Lymphocytes / immunology
  • CD4-Positive T-Lymphocytes / immunology
  • Cytokines / biosynthesis
  • Echinococcosis, Hepatic / immunology*
  • Echinococcus / immunology*
  • Female
  • Immune Tolerance
  • In Vitro Techniques
  • Interferon-gamma / biosynthesis
  • Interleukin-2 / biosynthesis
  • Lymphocyte Activation
  • Mice
  • Mice, Inbred C57BL
  • Mitogens / pharmacology
  • Spleen / immunology
  • T-Lymphocytes / immunology*
  • Time Factors

Substances

  • Antigens, Helminth
  • Cytokines
  • Interleukin-2
  • Mitogens
  • Interferon-gamma