TLR4 single-nucleotide polymorphisms alter mucosal cytokine and chemokine patterns in Mexican patients with Helicobacter pylori-associated gastroduodenal diseases
Copyright policy )TLR4 single-nucleotide polymorphisms alter mucosal cytokine and chemokine patterns in Mexican patients with Helicobacter pylori-associated gastroduodenal diseases
Helicobacter pylori is associated with peptic ulcer and gastric adenocarcinoma. Toll-like receptors (TLRs) participate in H. pylori recognition, and single-nucleotide polymorphisms (SNPs) in TLRs are associated with impaired immune response. We aimed to evaluate the association of TLR2/R753Q and TLR4/D299G/T399I SNPs with gastroduodenal diseases; and study the effect of SNPs on cytokine and chemokine expression in the gastric mucosa. Study included 450 Mexican patients with gastroduodenal diseases. SNPs in TLRs 2 and 4 genes were analyzed by allele-specific PCR. Cytokines and chemokines were assessed by qRT-PCR and immunoassay. TLR4/D299G/T399I polymorphisms were more frequent in duodenal ulcer and showed a trend in gastric cancer, when compared with non-atrophic gastritis. Patients with TLR4 polymorphisms expressed significantly lower levels of IL-1beta, IL-6, IL-8 and GRO-alpha; and higher levels of TNF-alpha, IL-10, MCP-1 and MIP-1alpha . SNPs in TLR4 gene had an association with severe H. pylori-associated disease and with modified pattern of inflammatory cytokines and chemokines in the gastric mucosa. These results suggest that TLR4 SNPs contributes importantly to the clinical outcome of H. pylori infection.
Adult, Male, Metaplasia, Helicobacter pylori, Middle Aged, Polymorphism, Single Nucleotide, Toll-Like Receptor 2, Helicobacter Infections, Toll-Like Receptor 4, Stomach Neoplasms, Case-Control Studies, Duodenal Ulcer, Gastritis, Cytokines, Humans, Female, Chemokines, Aged
Adult, Male, Metaplasia, Helicobacter pylori, Middle Aged, Polymorphism, Single Nucleotide, Toll-Like Receptor 2, Helicobacter Infections, Toll-Like Receptor 4, Stomach Neoplasms, Case-Control Studies, Duodenal Ulcer, Gastritis, Cytokines, Humans, Female, Chemokines, Aged
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