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Antibody response in CD4-depleted mice after immunization or during early infection with Echinococcus granulosus.

Abstract
The aims of this work were to investigate the existence of T-independent antigens in Echinococcus granulosus protoscoleces and to evaluate the relative contribution of T-independent stimulation to the overall antibody response in early infection. Mice depleted of CD4(+)-cells were immunized with protoscolex somatic antigens (PSA) or infected with E. granulosus protoscoleces (PSC). Results showed that the response of CD4-depleted immunized mice had the expected characteristics of a T-independent stimulation and that such T-independent stimulation was important mainly during primary response. During infection absence of CD4(+)-cells affected mainly the secretion of all IgG subclasses with the exception of IgG3 and IgM. To carry out a preliminary isolation of PSC T-independent antigens we prepared a carbohydrate enriched fraction from protoscolex antigens, using a monoclonal antibody specific for the carbohydrate moiety Gal alpha(1,4)Gal highly expressed in PSC. This fraction was mitogenic for naive mouse splenocytes and was recognized by a high percentage of the specific antibodies secreted by CD4-depleted immunized or infected mice. In summary, these results suggest that E. granulosus protoscoleces contain immunogenic T-independent antigens. Primary antibody responses to protoscolex somatic antigens and the production of IgM and IgG3 in early infection would be mainly stimulated by a T-independent mechanism.
AuthorsA Baz, A Richieri, A Puglia, A Nieto, S Dematteis
JournalParasite immunology (Parasite Immunol) Vol. 21 Issue 3 Pg. 141-50 (Mar 1999) ISSN: 0141-9838 [Print] England
PMID10205794 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
Chemical References
  • Antibodies, Helminth
  • Antigens, Helminth
  • Carbohydrates
Topics
  • Animals
  • Antibodies, Helminth (immunology)
  • Antigens, Helminth (immunology)
  • CD4-Positive T-Lymphocytes (immunology)
  • Carbohydrates (immunology)
  • Echinococcus (immunology)
  • Immunization
  • Lymphocyte Depletion
  • Mice
  • Mice, Inbred BALB C

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