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Reduced suppressor cell activity in intestinal lymphocytes from patients with Crohn's disease.

Abstract
Suppressor cell activity in intestinal lymphocytes was investigated by a coculture assay with autologous peripheral blood lymphocytes. Greater than 45% suppression was found in 7 out of 10 patients without Crohn's disease. Reduced suppressor cell activity was found in intestinal lymphocytes isolated from 7 out of 8 patients with Crohn's disease. Intestinal lymphocytes from patients with Crohn's disease demonstrated a significantly greater response to phytohemagglutinin-P than lymphocytes isolated from non-Crohn's patients. However, this difference could not be explained by alterations in proportions of T lymphocytes as intestinal T lymphocytes from non-Crohn's disease patients (54%) were not significantly different from those found in patients with Crohn's disease (57%). Indomethacin, a prostaglandin synthetase inhibitor, decreased the proliferative response of intestinal lymphocytes to phytohemagglutinin-P whereas the response of peripheral blood lymphocytes was enhanced, thus providing further evidence that intestinal lymphocytes may represent a functionally distinct population from circulating lymphocytes. Cimetidine, a H2-receptor antagonist, had no effect on the response of intestinal lymphocytes to phytohemagglutinin-P. These results provide evidence to support the concept that disturbed immunoregulation at the mucosal level is found in Crohn's disease.
AuthorsR L Goodacre, J Bienenstock
JournalGastroenterology (Gastroenterology) Vol. 82 Issue 4 Pg. 653-8 (Apr 1982) ISSN: 0016-5085 [Print] United States
PMID7060886 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
Chemical References
  • Mitomycins
  • Phytohemagglutinins
  • Cimetidine
  • Indomethacin
Topics
  • Cimetidine (pharmacology)
  • Crohn Disease (immunology)
  • Humans
  • Indomethacin (pharmacology)
  • Intestinal Mucosa (cytology)
  • Lymphocyte Activation (drug effects)
  • Lymphocytes (drug effects, immunology)
  • Mitomycins (pharmacology)
  • Phytohemagglutinins (pharmacology)
  • Rosette Formation

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