Persistent H. pylori colonization in early acquisition age of mice related with higher gastric sialylated Lewis x, IL-10, but lower interferon- expressions

Yao Jong Yang, Hsiao Bai Yang, Jiunn Jong Wu, Bor Shyang Sheu

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3 Citations (Scopus)

Abstract

Background. H. pylori infection is less prevalent in childhood. This study validated whether the rates of H. pylori colonization depend on different acquisition ages, and correlate with the different gastric Lewis antigens or cytokine expressions after H. pylori acquisition. Methods. We applied a young (7-day-old) C57BL/6 mice group (n = 50) and adult (6-week-old) C57BL/6 mice group (n = 50). In each group, 30 mice were challenged with H. pylori and 20 mice served as nave control. The success of H. pylori colonization was assessed on the 2ndweek and the 8thweek, respectively. The intensity of the Lewis x, sialylated Lewis x(sialyl-Lex), and cytokine expressions, including TNF-, IFN-, IL-6, IL-10, and IL-1, were immunochemically stained and graded. Results. On the 2ndweek after H. pylori challenge, the colonization rates of H. pylori were similar between the young mice group and the adult mice group (89% vs. 100%, P > 0.05). However, on the 8thweek, the H. pylori colonization rate was significantly lower in the young mice group than in the adult mice group (53% vs. 95%, P = 0.003). On the 8thweek, the young mice with a persistence of H. pylori colonization had higher sialyl-Lex, higher IL-10, and lower IFN- than those of the mice that lost colonization during the 2ndto the 8thweek (P < 0.05). Conclusion. The persistence of H. pylori colonization could be an acquisition-age determinant process. After H. pylori exposure at an early acquisition age, the host response with a higher sialyl-Lexand IL-10, but a lower IFN- correlates to the consequent persistence of H. pylori colonization.

Original languageEnglish
Article number34
JournalJournal of biomedical science
Volume16
Issue number1
DOIs
Publication statusPublished - 2009

All Science Journal Classification (ASJC) codes

  • Endocrinology, Diabetes and Metabolism
  • Molecular Biology
  • Clinical Biochemistry
  • Cell Biology
  • Biochemistry, medical
  • Pharmacology (medical)

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