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

Citation
C. Prinz et al., Key importance of the Helicobacter pylori adherence factor blood group antigen binding adhesin during chronic gastric inflammation, CANCER RES, 61(5), 2001, pp. 1903-1909
Citations number
52
Categorie Soggetti
Oncology,"Onconogenesis & Cancer Research
Journal title
CANCER RESEARCH
ISSN journal
00085472 → ACNP
Volume
61
Issue
5
Year of publication
2001
Pages
1903 - 1909
Database
ISI
SICI code
0008-5472(20010301)61:5<1903:KIOTHP>2.0.ZU;2-V
Abstract
Helicobacter pylori has been assigned as a class 1 carcinogen because of it s 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 antige n binding adhesin (BabA) targeting Lewis(b) antigens, have been associated previously with distal gastric adenocarcinoma (M. Gerhard et al., Proc. Nat l, Acad. Sci, USA. 96: 12778-12783, 1999) and may therefore also be related to lesions preceding gastric cancer. Antral and corpus biopsies were colle cted from 451 patients: 151 were H. pylori positive, as determined by PCR, Gastric biopsies were histologically evaluated for activity of gastritis (G 0-G3, granulocyte infiltration), chronicity of gastritis (L1-L3, lymphocyte infiltration), and the presence of IM and/or AT according to the Sydney cl assification. Simultaneously, the presence of bacterial genes encoding viru lence and adherence factors (vacAs1/s2, cagA, and babA2) was determined by PCR, The presence of cagA+ and vacAs1 (alone or combined) both correlated w ith activity and chronicity of gastritis: (P < 0.05); however, the overall prevalence of these genes was 60 or 72%, respectively, and was thus relativ ely 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 prese nce of type 1 strains) that were also babA2 positive were detected more fre quently in patients with severe histological alterations (such as G3, IM, o r AT) compared with subjects without these changes (P < 0.01), cagA+/vacAs1 + strains that were babA2 negative, however, lacked a significant correlati on with severe histological changes, activity, or chronicity of gastritis i n antrum and corpus. Adherence of H. pylori via BabA appears to be of impor tance for efficient delivery of VacA and CagA and may play a special role i n the pathogenesis of severe histological changes.