Literature DB >> 3217130

Enzyme-linked immunosorbent assay for Giardia-specific IgA in mouse intestinal secretions.

M F Heyworth1, J E Kung, A B Caplin.   

Abstract

We describe an ELISA for trophozoite-specific IgA in the intestinal secretions of mice infected with Giardia muris. Using this method, trophozoite-specific IgA was demonstrated in intestinal secretions of Giardia-infected immunocompetent BALB/c mice. Such antibody was undetectable in the intestinal secretions of Giardia-infected athymic (nude) mice. Immunocompetent BALB/c mice are able to clear G. muris infection whereas nude mice are not. The study provides evidence that the chronicity of G. muris infection in nude mice results from lack of intestinal trophozoite-specific IgA in these animals. By means of the ELISA, trophozoite-specific IgA was demonstrated in intestinal secretions from immunocompetent mice in the absence of protease inhibitors.

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Year:  1988        PMID: 3217130     DOI: 10.1111/j.1365-3024.1988.tb00257.x

Source DB:  PubMed          Journal:  Parasite Immunol        ISSN: 0141-9838            Impact factor:   2.280


  4 in total

1.  Comparison of antibody and cytokine responses to primary Giardia muris infection in H-2 congenic strains of mice.

Authors:  P Venkatesan; R G Finch; D Wakelin
Journal:  Infect Immun       Date:  1996-11       Impact factor: 3.441

2.  Recognition of a 30,000 MW antigen of Giardia muris trophozoites by intestinal IgA from Giardia-infected mice.

Authors:  M F Heyworth; J Pappo
Journal:  Immunology       Date:  1990-08       Impact factor: 7.397

3.  In vitro synthesized immunoglobulin A from nu/+ and reconstituted nu/nu mice against a dominant surface antigen of Giardia lamblia.

Authors:  B Gottstein; P Deplazes; I Tanner
Journal:  Parasitol Res       Date:  1993       Impact factor: 2.289

4.  Antimicrobial action of antibodies against Giardia muris trophozoites.

Authors:  M Belosevic; G M Faubert; S Dharampaul
Journal:  Clin Exp Immunol       Date:  1994-03       Impact factor: 4.330

  4 in total

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