RT Journal Article SR Electronic T1 Relation between clinical presentation,Helicobacter pylori density, interleukin 1β and 8 production, and cagA status JF Gut JO Gut FD BMJ Publishing Group Ltd and British Society of Gastroenterology SP 804 OP 811 DO 10.1136/gut.45.6.804 VO 45 IS 6 A1 Y Yamaoka A1 T Kodama A1 M Kita A1 J Imanishi A1 K Kashima A1 D Y Graham YR 1999 UL http://gut.bmj.com/content/45/6/804.abstract AB BACKGROUND It is not known whethercagA+ Helicobacter pylori in duodenal ulcer (DU) have enhanced virulence compared with non-DU cagA+ H pylori. AIMS To investigate the relation between presentation, H pylori density, interleukin 1β (IL-1β) and IL-8 production, andcagA status.METHODS Fifty DU and 50 gastritis patients with cagA+ H pylori and 11 with cagA− infections were studied. Bacterial density and cytokine production were assessed using the same biopsies. Cytokine production was also measured from supernatants of medium following coculture of H pylori with MKN-45 cells.RESULTS There was no relation between H pylori density andcagA status. There was a dose dependent relation between mucosal cytokine levels and density ofcagA+ H pylori. H pylori density increased to a threshold, followed by a rapid increase in cytokines and then a plateau. IL-1β and IL-8 levels in the antrum were greater in DU than in gastritis; in the corpus the cytokine level/H pylori differed irrespective of similar H pylori densities. However, cytokine production was similar in vitro, independent of presentation or biopsy site, suggesting that host factors are critical determinants of the inflammatory response. Mucosal IL-8 and IL-1β levels were low withcagA− andcagA+, cagE− H pylori infections.CONCLUSIONS The increase in antral IL-1β and IL-8 production and inflammation in DU is related to increased numbers of bacteria and not to an increase in cytokine production per cagA+ isolate. There was no evidence of enhanced virulence of H pylorifrom DU compared with cagA+ non-DUH pylori. DUduodenal ulcerILinterleukinMNCmononuclear cellPCRpolymerase chain reactionPMNpolymorphonuclear cell