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HELICOBACTER PYLORI VIRULENCE GENES AND HOST IL-1RN AND IL-1β GENES INTERPLAY IN FAVOURING THE DEVELOPMENT OF PEPTIC ULCER AND INTESTINAL METAPLASIA
Helicobacter pylori infection outcome might depend on genotypic polymorphisms of both the bacterium and the host. We ascertained: (1) the functionality of H. pylori oipA gene; (2) the polymorphism of the host interleukin ( IL-1 β) gene (−31 C/T) and of the IL-1RN gene (intron 2 VNTR); (3) the associ...
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Published in: | Cytokine (Philadelphia, Pa.) Pa.), 2002, Vol.18 (5), p.242-251 |
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Main Authors: | , , , , , , , , , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Online Access: | Get full text |
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Summary: | Helicobacter pylori
infection outcome might depend on genotypic polymorphisms of both the bacterium and the host. We ascertained: (1) the functionality of
H. pylori oipA
gene; (2) the polymorphism of the host
interleukin
(
IL-1
β) gene (−31 C/T) and of the
IL-1RN
gene (intron 2 VNTR); (3) the association between the above genes and the histological and pathological outcome of
H. pylori
infection. One hundred and sixty-five
H. pylori
positive and 137
H. pylori
negative subjects (23 gastric adenocarcinoma, 58 peptic ulcer, 221 gastritis) were studied.
oipA
was sequenced,
IL-1
β was RFLP analysed. Antral and body mucosal biopsies were histologically evaluated. Functional
oipA
genes were correlated with
cagA
gene; both genes were significantly associated with gastritis activity, peptic ulcer and gastric adenocarcinoma. In these patients heterozygous
IL-1RN
1/2 and
IL-1
β C/T genotypes were more frequent than in gastritis patients. Intestinal metaplasia was associated with
cagA
, functional
oipA
and
IL-1RN
2 allele. In conclusion, peptic ulcer and the preneoplastic intestinal metaplasia are associated with
H. pylori
virulence genes and with
IL-1RN
2 host allele. An interplay between bacterial virulence factors and cytokines genotypes, is probably the main route causing
H. pylori
infection to lead to benign mild disease, benign severe disease or preneoplastic lesions. |
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ISSN: | 1043-4666 1096-0023 |
DOI: | 10.1006/cyto.2002.0891 |