Literature DB >> 11280745

Key importance of the Helicobacter pylori adherence factor blood group antigen binding adhesin during chronic gastric inflammation.

C Prinz1, M Schöniger, R Rad, I Becker, E Keiditsch, S Wagenpfeil, M Classen, T Rösch, W Schepp, M Gerhard.   

Abstract

Helicobacter pylori has been assigned as a class I carcinogen because of its relation to gastric adenocarcinoma. Chronic H. pylori infection may lead to severe gastritis, glandular atrophy (AT), and intestinal metaplasia (IM). Strains secreting the vacuolating toxin VacA and producing the cytotoxin-associated antigen CagA (type 1 strains), as well as the blood group antigen binding adhesin (BabA) targeting Lewis(b) antigens, have been associated previously with distal gastric adenocarcinoma (M. Gerhard et al., Proc. Natl. Acad. Sci. USA, 96: 12778-12783, 1999) and may therefore also be related to lesions preceding gastric cancer. Antral and corpus biopsies were collected from 451 patients; 151 were H. pylori positive, as determined by PCR. Gastric biopsies were histologically evaluated for activity of gastritis (G0-G3, granulocyte infiltration), chronicity of gastritis (L1-L3, lymphocyte infiltration), and the presence of IM and/or AT according to the Sydney classification. Simultaneously, the presence of bacterial genes encoding virulence and adherence factors (racAs1/s2, cagA, and babA2) was determined by PCR. The presence of cagA+ and vacAs1 (alone or combined) both correlated with activity and chronicity of gastritis (P < 0.05); however, the overall prevalence of these genes was 60 or 72%, respectively, and was thus relatively frequent. The babA2 gene, encoding the adhesin BabA, was detected in 38% of infected patients and was correlated with the activity of gastritis in antrum and corpus (P < 0.005). cagA+/vacAs1+ strains (suggesting the presence of type 1 strains) that were also babA2 positive were detected more frequently in patients with severe histological alterations (such as G3, IM, or AT) compared with subjects without these changes (P < 0.01). cagA+/vacAs1+ strains that were babA2 negative, however, lacked a significant correlation with severe histological changes, activity, or chronicity of gastritis in antrum and corpus. Adherence of H. pylori via BabA appears to be of importance for efficient delivery of VacA and CagA and may play a special role in the pathogenesis of severe histological changes.

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Year:  2001        PMID: 11280745

Source DB:  PubMed          Journal:  Cancer Res        ISSN: 0008-5472            Impact factor:   12.701


  49 in total

1.  Helicobacter pylori infection is associated with a high incidence of intestinal metaplasia in the gastric mucosa of patients at inner-city hospitals in New York.

Authors:  J Schneller; R Gupta; J Mustafa; R Villanueva; E W Straus; R D Raffaniello
Journal:  Dig Dis Sci       Date:  2006-10       Impact factor: 3.199

2.  Helicobacter pylori outer membrane proteins and gastric inflammation.

Authors:  A Dossumbekova; C Prinz; M Gerhard; L Brenner; S Backert; J G Kusters; R M Schmid; R Rad
Journal:  Gut       Date:  2006-09       Impact factor: 23.059

3.  Helicobacter pylori outer membrane proteins and gastroduodenal disease.

Authors:  Y Yamaoka; O Ojo; S Fujimoto; S Odenbreit; R Haas; O Gutierrez; H M T El-Zimaity; R Reddy; A Arnqvist; D Y Graham
Journal:  Gut       Date:  2005-12-01       Impact factor: 23.059

4.  Relationship between Helicobacter pylori babA2 status with gastric epithelial cell turnover and premalignant gastric lesions.

Authors:  J Yu; W K Leung; M Y Y Go; M C W Chan; K F To; E K W Ng; F K L Chan; T K W Ling; S C S Chung; J J Y Sung
Journal:  Gut       Date:  2002-10       Impact factor: 23.059

Review 5.  Exploring alternative treatments for Helicobacter pylori infection.

Authors:  Guadalupe Ayala; Wendy Itzel Escobedo-Hinojosa; Carlos Felipe de la Cruz-Herrera; Irma Romero
Journal:  World J Gastroenterol       Date:  2014-02-14       Impact factor: 5.742

Review 6.  Helicobacter pylori infection: host immune response, implications on gene expression and microRNAs.

Authors:  Aline Cristina Targa Cadamuro; Ana Flávia Teixeira Rossi; Nathália Maciel Maniezzo; Ana Elizabete Silva
Journal:  World J Gastroenterol       Date:  2014-02-14       Impact factor: 5.742

Review 7.  Roles of Helicobacter pylori BabA in gastroduodenal pathogenesis.

Authors:  Yoshio Yamaoka
Journal:  World J Gastroenterol       Date:  2008-07-21       Impact factor: 5.742

8.  Protein interaction network related to Helicobacter pylori infection response.

Authors:  Kyu Kwang Kim; Han Bok Kim
Journal:  World J Gastroenterol       Date:  2009-09-28       Impact factor: 5.742

9.  Cytokine gene polymorphisms influence mucosal cytokine expression, gastric inflammation, and host specific colonisation during Helicobacter pylori infection.

Authors:  R Rad; A Dossumbekova; B Neu; R Lang; S Bauer; D Saur; M Gerhard; C Prinz
Journal:  Gut       Date:  2004-08       Impact factor: 23.059

10.  ABH and Lewis antigen distributions in blood, saliva and gastric mucosa and H pylori infection in gastric ulcer patients.

Authors:  Luisa Caricio Martins; Tereza Cristina de Oliveira Corvelo; Henrique Takeshi Oti; Rosane do Socorro Pompeu Loiola; Delia Cristina Figueira Aguiar; Katarine Antonia dos Santos Barile; Renata Kelly Costa do Amaral; Hivana Patricia Melo Barbosa; Amanda Alves Fecury; Juciclayton Tavares de Souza
Journal:  World J Gastroenterol       Date:  2006-02-21       Impact factor: 5.742

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