IgA-containing circulating immune complexes in gluten-sensitive enteropathy.

Journal Article (Journal Article)

Since mucosal immune response involving IgA may be particularly important in the pathogenesis of gluten-sensitive enteropathy (GSE), we examined the sera of 22 patients with GSE for IgA-containing circulating immune complexes using a sensitive radioimmunoassay, the Raji cell assay for IgA-containing circulating immune complexes. The Raji cell assay for IgG-containing circulating immune complexes and the 125I-C1q-binding assay were also used to measure IgG- or IgM-containing circulating immune complexes in these patients. Ten of 22 (45%) patients had IgA-containing circulating immune complexes, while 11 of 22 (50%) had IgG- or IgM-containing circulating immune complexes. Thirteen of 22 (59%) patients had circulating immune complexes detected by at least one of the assays used. Neither the presence nor level of immune complexes correlated with disease activity in any of the patients studied. Five patients, whose disease was well controlled on a gluten-free diet, were studied serially during dietary challenge with gluten. It was found that IgA-containing circulating immune complexes did not develop or increase in amount in the serum of these patients despite the induction of gastrointestinal symptoms. In addition, no significant change in IgG- or IgM- containing circulating immune complexes occurred in any of the challenged patients. No significant abnormalities of serum complement levels (C3, C4, factor B) were detected in any of the patients including those challenged with gluten. Sucrose density-gradient ultracentrifugation studies revealed that the IgA-containing circulating immune complexes had sedimentation characteristics between 9S and 13S. The presence of circulating immune complexes in only 59% of patients with GSE, their lack of correlation with disease activity, and their failure to change during dietary gluten challenge suggests that circulating immune complexes do not play a primary role in the pathogenesis of GSE.

Full Text

Duke Authors

Cited Authors

  • Hall, RP; Strober, W; Katz, SI; Lawley, TJ

Published Date

  • August 1981

Published In

Volume / Issue

  • 45 / 2

Start / End Page

  • 234 - 239

PubMed ID

  • 7318253

Pubmed Central ID

  • PMC1537367

International Standard Serial Number (ISSN)

  • 0009-9104

Language

  • eng

Conference Location

  • England