4.7 Article

High levels of Crohn's disease-associated anti-microbial antibodies are present and independent of colitis in chronic granulomatous disease

期刊

CLINICAL IMMUNOLOGY
卷 138, 期 1, 页码 14-22

出版社

ACADEMIC PRESS INC ELSEVIER SCIENCE
DOI: 10.1016/j.clim.2010.08.003

关键词

Chronic granulomatous disease; Hyper IgE Syndrome; Inflammatory bowel disease; Serum antimicrobial antibodies; Colitis; Innate immunity

资金

  1. National Institutes of Health [AI-101093, AI-467320, AI-48693, T32 AI007605-07]
  2. National Institute of Allergy and Infectious Diseases [03-22]
  3. Division of Intramural Research, National Institute of Allergy and Infectious Diseases, National Institutes of Health
  4. National Institutes of Health/National Institute of Allergy and Infectious Diseases
  5. Baxter Therapeutics
  6. NATIONAL INSTITUTE OF ALLERGY AND INFECTIOUS DISEASES [R21AI101093, U24AI086037, R18AI048693, T32AI007605, ZIAAI000645, ZIAAI000646] Funding Source: NIH RePORTER
  7. NATIONAL INSTITUTE OF DIABETES AND DIGESTIVE AND KIDNEY DISEASES [P01DK046763] Funding Source: NIH RePORTER

向作者/读者索取更多资源

Chronic granulomatous disease (CGD) and inflammatory bowel disease (IBD) have overlapping gastrointestinal manifestations. Serum antibodies to intestinal microbial antigens in IBD are thought to reflect a loss of tolerance in the setting of genetically encoded innate immune defects. CGD subjects studied here, with or without colitis, had considerably higher levels of ASCA IgA, ASCA IgG, anti-OmpC, anti-I2, and anti-CBir1, but absent to low pANCA, compared to IBD-predictive cutoffs. Higher antibody levels were not associated with a history of colitis. Except for higher ASCA IgG in subjects <18 years, antibody levels were not age-dependent. In comparison, 7 HIES subjects expressed negative to low antibody levels to all of these antigens; none had colitis. Our results suggest that markedly elevated levels of antimicrobial antibodies in CGD do not correlate with a history of colitis but may reflect a specific defect in innate immunity in the face of chronic antigenic stimulation. (C) 2010 Elsevier Inc. All rights reserved.

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