Gastric mucosal interleukin-8 and IL-8 antibody concentrations related to prevailing Helicobacter pylori infections. A Danish-Albanian study

Dan Med Bull. 1999 Jun;46(3):249-52.

Abstract

Objectives: Helicobacter pylori (H. pylori) appears to initiate an inflammatory cascade. Thus, phagocytes are accumulated in the gastric mucosa, in inflammatory conditions. Further, a potent chemotactic mediator, interleukin 8 (IL-8) is synthesized at such sites. The recently described IL-8 autoantibodies may, however, counteract the pro-inflammatory actions of IL-8. The aim was to study the correlation between H. pylori infection and IL-8, together with IL-8 autoantibodies in two different populations from a developed and a developing country.

Methods: Two different endoscopically characterized populations (65 Danes and 89 Albanians) were examined. IL-8 and IL-8 autoantibodies were detected by ELISA techniques, and H. pylori was identified by histological examinations.

Results: Significantly more Albanian controls and dyspeptic patients (80 out of 89 persons) were H. pylori positive as compared to 24 of 65 Danes (p < 0.001). The median IL-8 level among Albanian controls 349 pg/mg protein was significantly higher than among Danes < 61 pg/mg protein (p < 0.001), and was at the same level as found in Danish peptic ulcer patients (p > 0.05). Further, H. pylori positive patients from both countries had significantly higher levels of IL-8 as compared to H. pylori negative patients (p < 0.001). However, significantly higher levels of IL-8 autoantibodies were found in the Albanian sub-population (median 138 O.D. units versus 52 O.D. units among Danes) (p < 0.001).

Conclusions: In H. pylori related disorders, a high mucosal IL-8 production has been found. However, this investigation further demonstrates higher levels of IL-8 autoantibodies among dyspeptic patients from a developing country, which might possibly counteract the pro-inflammatory actions of IL-8 by binding the molecule. The physiological significance of an altered immune response as described here needs to be elucidated in future studies.

Publication types

  • Multicenter Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adolescent
  • Adult
  • Aged
  • Autoantibodies / metabolism*
  • Duodenal Ulcer / immunology
  • Duodenal Ulcer / metabolism
  • Duodenal Ulcer / microbiology
  • Duodenitis / immunology
  • Duodenitis / metabolism
  • Duodenitis / microbiology
  • Female
  • Gastric Mucosa / immunology*
  • Gastric Mucosa / metabolism*
  • Gastritis / immunology
  • Gastritis / metabolism
  • Gastritis / microbiology
  • Helicobacter Infections / immunology*
  • Helicobacter Infections / metabolism*
  • Helicobacter pylori*
  • Humans
  • Interleukin-8 / immunology*
  • Interleukin-8 / metabolism*
  • Male
  • Middle Aged
  • Stomach Ulcer / immunology
  • Stomach Ulcer / metabolism
  • Stomach Ulcer / microbiology

Substances

  • Autoantibodies
  • Interleukin-8