Association of peptic ulcer with increased expression of Lewis antigens but not cagA, iceA, and vacA in Helicobacter pylori isolates in an Asian population

Citation
Py. Zheng et al., Association of peptic ulcer with increased expression of Lewis antigens but not cagA, iceA, and vacA in Helicobacter pylori isolates in an Asian population, GUT, 47(1), 2000, pp. 18-22
Citations number
34
Categorie Soggetti
Gastroenerology and Hepatology","da verificare
Journal title
GUT
ISSN journal
00175749 → ACNP
Volume
47
Issue
1
Year of publication
2000
Pages
18 - 22
Database
ISI
SICI code
0017-5749(200007)47:1<18:AOPUWI>2.0.ZU;2-V
Abstract
Background-Studies in Western populations suggest that cagA, iceA, and vacA gene status in helicobacter pylori isolates is associated with increased v irulence and peptic ulcer disease. Aim-To investigate the relationship between peptic ulcer and expression of Lewis (Le) antigens as well as cagA, iceA, and vacA in H pylori isolates in Singapore.;Methods-Expression of Le antigens in H pylori isolates obtained from patients with dyspepsia was measured by enzyme Linked immunosorbent a ssay. The cagA, iceA, and vacA status was determined by polymerase chain re action. Results-Of 108 H pylori isolates, 103 (95.4%) expressed Le(x) and/or Le(y), while Le(a) and Le(b) were expressed in 23 (21.3%) and 47 (43.5%) isolates , respectively. Expression of two or more Le antigens (Le(x), Le(y), Le(a), or Le(b)) was significantly higher in H pylori isolated from ulcer patient s than in non-ulcer patients (89.6% v 73.2%, p=0.035). There were no signif icant differences in the prevalence of cagA or iceA1 in H pylori isolates f rom peptic ulcer and non-ulcer patients (86.6% v 90.2% for cagA; 70.1% v 68 .3% for iceA1), and no association of peptic ulcer with any specific vacA g enotype. Conclusions-The present study indicates that peptic ulcer disease is associ ated with increased expression of Lewis antigens but not cagA, iceA, or vac A genotype in H pylori isolates in our population. This suggests that cagA, iceA, and vacA are not universal virulence markers, and that host-pathogen interactions are important in determining clinical outcome.