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Effect of corticosteroids on suppressor-cell activity in "autoimmune" and viral chronic active hepatitis.

Abstract
We detected a severe defect in concanavalin A-induced suppressor-cell activity in 22 patients with "autoimmune" chronic active hepatitis and in 26 patients with hepatitis B surface antigen (HBsAg)-positive chronic active hepatitis, as compared with 20 control subjects (P less than 0.01). Normal values were observed in 21 patients with "autoimmune" hepatitis in whom a remission had been induced and maintained by treatment with prednisolone. When lymphocytes from patients with autoimmune chronic active hepatitis were preincubated with low-dose prednisolone in vitro, suppressor-cell activity was substantially improved (P less than 0.01), but no clear effect of prednisolone was seen in cells from patients with HBsAg-positive chronic active hepatitis. The loss of suppressor-cell activity in chronic active hepatitis may allow liver damage to continue, and the reversal of the defect in the autoimmune form of the disease by administration of low-dose prednisolone provides a plausible explanation for the efficacy of this treatment. The contrasting in vitro responses to prednisolone in autoimmune and HBsAg-positive chronic active hepatitis suggest that the fundamental nature of the suppressor-cell defect may be different in these two forms of the disease.
AuthorsK T Nouri-Aria, J E Hegarty, G J Alexander, A L Eddleston, R Williams
JournalThe New England journal of medicine (N Engl J Med) Vol. 307 Issue 21 Pg. 1301-4 (Nov 18 1982) ISSN: 0028-4793 [Print] United States
PMID6215581 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
Chemical References
  • Adrenal Cortex Hormones
  • Hepatitis B Surface Antigens
  • Prednisolone
Topics
  • Adrenal Cortex Hormones (pharmacology, therapeutic use)
  • Autoimmune Diseases (drug therapy, immunology)
  • Chronic Disease
  • Hepatitis (drug therapy, immunology)
  • Hepatitis B (drug therapy, immunology)
  • Hepatitis B Surface Antigens (analysis)
  • Humans
  • Prednisolone (pharmacology)
  • T-Lymphocytes, Regulatory (drug effects, immunology)

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