Literature DB >> 3200186

The use of serology to diagnose active Campylobacter pylori infection.

H M Mitchell1, A Lee, J Berkowicz, T Borody.   

Abstract

A serological test that predicts accurately active Campylobacter pylori infection in the human stomach has been developed and validated by means of serum from 189 patients who were undergoing endoscopy in Sydney. Our enzyme-linked immunosorbent assay (ELISA) has a sensitivity of 100% and a specificity of 94%. An important part of the test is the inclusion of a simple absorption step with C. jejuni for those sera whose results are close to the cut-off point for positivity. This has been shown to be particularly relevant in epidemiological studies on populations that are likely to be exposed to C. jejuni continually. For example, by means of the ELISA test without an absorption step, the infection rate in Papua New Guineans was shown to be 56%, whereas use of the validated test showed the infection rate to be 25%. Compared with an age-matched normal control group of Australians, this still is higher. These studies suggest a need for the reappraisal of some of the reported epidemiological data. The development of a validated diagnostic test that is a highly-accurate predictor of active C. pylori infection will be useful for epidemiological studies, particularly for comparative studies among populations that are known to differ significantly in the incidence of stomach disease. However, routine use of this test in diagnosis in general practice awaits the definition of more precise markers of C. pylori-associated symptomatology and the development of improved regimens for the treatment of C. pylori infections.

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Year:  1988        PMID: 3200186     DOI: 10.5694/j.1326-5377.1988.tb120800.x

Source DB:  PubMed          Journal:  Med J Aust        ISSN: 0025-729X            Impact factor:   7.738


  21 in total

Review 1.  An assessment of serological tests for detection of Helicobacter pylori.

Authors:  H von Wulffen
Journal:  Eur J Clin Microbiol Infect Dis       Date:  1992-07       Impact factor: 3.267

2.  Murine splenocytes induce severe gastritis and delayed-type hypersensitivity and suppress bacterial colonization in Helicobacter pylori-infected SCID mice.

Authors:  K A Eaton; S R Ringler; S J Danon
Journal:  Infect Immun       Date:  1999-09       Impact factor: 3.441

3.  Comparison of rapid office-based serology with formal laboratory-based ELISA testing for diagnosis of Helicobacter pylori gastritis.

Authors:  J A Kroser; D O Faigel; E E Furth; D C Metz
Journal:  Dig Dis Sci       Date:  1998-01       Impact factor: 3.199

Review 4.  Diagnosis of Helicobacter pylori.

Authors:  U Blecker; D I Mehta
Journal:  Indian J Pediatr       Date:  1997 Nov-Dec       Impact factor: 1.967

5.  The endotoxin of Helicobacter pylori is a modulator of host-dependent gastritis.

Authors:  T Sakagami; J Vella; M F Dixon; J O'Rourke; F Radcliff; P Sutton; T Shimoyama; K Beagley; A Lee
Journal:  Infect Immun       Date:  1997-08       Impact factor: 3.441

6.  Immunoblot analysis of humoral immune response to Helicobacter pylori in children with and without duodenal ulcer.

Authors:  G A Rocha; A M Oliveira; D M Queiroz; A S Carvalho; A M Nogueira
Journal:  J Clin Microbiol       Date:  2000-05       Impact factor: 5.948

7.  Antibody to cytotoxin in infection by Helicobacter pylori.

Authors:  R D Leunk; M A Ferguson; D R Morgan; D E Low; A E Simor
Journal:  J Clin Microbiol       Date:  1990-06       Impact factor: 5.948

8.  Importance of childhood socioeconomic status on the current prevalence of Helicobacter pylori infection.

Authors:  H M Malaty; D Y Graham
Journal:  Gut       Date:  1994-06       Impact factor: 23.059

9.  Use of a urea breath test versus invasive methods to determine the prevalence of Helicobacter pylori in Zaire.

Authors:  Y Glupczynski; L Bourdeaux; M Verhas; C DePrez; D DeVos; T Devreker
Journal:  Eur J Clin Microbiol Infect Dis       Date:  1992-04       Impact factor: 3.267

10.  Serodiagnosis of Helicobacter pylori infections with an enzyme immunoassay using the chromatographically purified 120 kilodalton protein.

Authors:  B Gerstenecker; B Eschweiler; H Vögele; H K Koch; U Hellerich; M Kist
Journal:  Eur J Clin Microbiol Infect Dis       Date:  1992-07       Impact factor: 3.267

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