Low seroprevalence of Helicobacter pylori antibodies in historical sera of patients with Crohn's disease.
- 1 January 1997
- journal article
- research article
- Published by Taylor & Francis in Scandinavian Journal of Gastroenterology
- Vol. 32 (7) , 712-718
- https://doi.org/10.3109/00365529708996523
Abstract
Background: Our aim was to determine the seroprevalence of Helicobacter pylori antibodies in historical sera from a large group of patients with Crohn's disease and to compare the findings with those of a control group of healthy blood transfusion donors. Methods: The historical sera from 386 patients with Crohn's disease were studied (serum age, 9.9 years; range, 0.4–21.6 years). Serum IgG and IgA H. pylori antibodies were measured with enzyme-linked immunosorbent assay. Western blots (detecting IgG only) were also used to study a subpopulation of the patients' sera and to assess the presence of cagA bands, indicating a cytotoxic variety of H. pylori. The serology of the Crohn's disease patients was compared with that of 277 age-matched controls. A longitudinal follow-up study of 14 IgG and IgA anti-ff. pyton-positive and 14 IgG- and IgA-negative Crohn's disease patients was also performed (mean follow-up, 7.6 years; range, 1.7–20.5 years). Results: Of the total Crohn's disease patients, 47 (12.2%) had IgG antibodies against H. pylori, 67 (17.4%) had IgA antibodies, and 31 (8.0%) had both IgG and IgA antibodies. The corresponding antibody positivities for the controls were 98 (35.4%) for IgG, 77 (27.8%) for IgA, and 64 (23.1%) for both IgG and IgA. When compared with the control group, the seroprevalence of H. pylori in the Crohn's disease patients was significantly lower (P < 0.002). In addition the relative IgG response of the patients was lower than the TgA response. The opposite was true for the controls. There was no difference in the absolute levels of H. pylori antibodies between patients and controls. In the follow-up study two patients initially IgG-positive for H. pylori became negative over time; these patients had been treated for their infection. The rest, who continued to be positive, were not treated. One patient who was initially IgA-positive also became IgA-negative over time. The follow-up group, who were initially IgG- and IgA-negative, remained IgG-negative with time, and two patients became IgA-positive. Findings of anti-H. pylori IgG were confirmed with Western blots. Furthermore, these showed that of the H. pylori-positive patients (indicated by their IgG positivity), 66% were infected with a cytotoxic (cagA-positive) variety, compared to 69.4% of the controls. Conclusions: Patients with Crohn's disease have a lower prevalence of H. pylori antibodies than an age-matched control group. There is a reversal of the relative IgG and IgA responses in Crohn's disease patients compared with the controls. Of the Crohn's disease patients with H. pylori most are infected with cytotoxic varieties, similar to controls.Keywords
This publication has 16 references indexed in Scilit:
- High frequency of helicobacter negative gastritis in patients with Crohn's disease.Gut, 1996
- Mucosal Inflammation and Disease inHelicobacter pyloriInfectionScandinavian Journal of Gastroenterology, 1996
- Inverse correlation between Helicobacter pylori infection and inflammatory bowel disease.Journal of Clinical Pathology, 1996
- Low prevalence of Helicobacter pylori in inflammatory bowel disease: association with sulphasalazine.Gut, 1994
- Seroconversion for Helicobacter pyloriThe Lancet, 1993
- Influence of age and Helicobacter pylori infection on serum pepsinogens in healthy blood transfusion donors.Gut, 1992
- Mucosal cell-mediated immunity to mycobacterial, enterobacterial and other microbial antigens in inflammatory bowel diseaseClinical and Experimental Immunology, 1992
- Long term serological surveillance after treatment of Helicobacter pylori infection.Gut, 1991
- Value of Serology (ELISA and Immunoblotting) for the Diagnosis of Campylobacter pylori InfectionDigestion, 1989
- Chronic gastritis—a pathogenetic approachThe Journal of Pathology, 1988