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Crohn's disease patients have more IgG-binding fecal bacteria than controls

Authors :
Simon D. Pouwels
Hermie J. M. Harmsen
Nicolaas A. Bos
Gerard Dijkstra
Anouk Funke
Microbes in Health and Disease (MHD)
Groningen Institute for Gastro Intestinal Genetics and Immunology (3GI)
Translational Immunology Groningen (TRIGR)
Source :
Clinical and vaccine immunology, 19(4), 515-521
Publication Year :
2012

Abstract

In Crohn's disease (CD), chronic gut inflammation leads to loss of mucosal barrier integrity. Subsequent leakage of IgG to the gut could produce an increase of IgG coating of intestinal bacteria. We investigated if there is more IgG coating in patients than in volunteers and whether this is dependent on the host IgG response or on the gut bacteria. Fecal and serum samples were obtained from 23 CD patients and 11 healthy volunteers. Both thein vivoIgG-coated fecal bacteria andin vitroIgG coating after serum addition were measured by flow cytometry and related to disease activity. The bacterial composition in feces was determined using fluorescencein situhybridization. The IgG-binding capacities ofEscherichia colistrains isolated from feces of patients and volunteers were assessed. The results showed that thein vivoIgG-coated fraction of fecal bacteria of patients was slightly larger than that of volunteers but significantly larger after incubation with either autologous or heterologous serum. This was dependent on the bacteria and independent of disease activity or the serum used. The presence of moreEnterobacteriaceaeand fewer faecalibacteria in patient feces was confirmed.E. coliisolates from patients bound more IgG than isolates from volunteers (P< 0.05) after the addition of autologous serum. Together, these results indicate that CD patients have more IgG-binding gut bacteria than healthy volunteers. We showed that the level of IgG coating depends on the bacteria and not on the serum used. Furthermore, CD patients have a strong specific immune response to their ownE. colibacteria.

Details

ISSN :
1556679X and 15566811
Volume :
19
Issue :
4
Database :
OpenAIRE
Journal :
Clinical and vaccine immunology : CVI
Accession number :
edsair.doi.dedup.....b0aa48b15fa932e043f5b9100496cc47