EFFECT OF INTERFERON THERAPY ON BILE-DUCT INFLAMMATION IN HEPATITIS-C

Citation
Bf. Banner et al., EFFECT OF INTERFERON THERAPY ON BILE-DUCT INFLAMMATION IN HEPATITIS-C, Virchows Archiv, 428(4-5), 1996, pp. 253-259
Citations number
22
Categorie Soggetti
Pathology
Journal title
ISSN journal
09456317
Volume
428
Issue
4-5
Year of publication
1996
Pages
253 - 259
Database
ISI
SICI code
0945-6317(1996)428:4-5<253:EOITOB>2.0.ZU;2-0
Abstract
Inflammation of the bile ducts was studied in liver biopsies from pati ents with chronic hepatitis C to determine whether the frequency of in flamed bile ducts changes with therapy and correlates with other histo logical variables and expression of class I and II MHC antigens on duc tal epithelium. Twenty patients treated at UMMC between 1991 and 1994 underwent needle biopsies of the liver before and after therapy with i nterferon alpha 2B (IFN). A complete response to therapy was defined a s a return to normal serum alanine aminotransferase levels occurring a nd persisting during therapy. The number of inflamed bile ducts/total ducts (%IBDs), presence of piecemeal necrosis and lymphoid aggregates, and grade of inflammation were assessed in each high power field in a ll areas with bile ducts. The frequencies of these variables were comp ared in cirrhotics and non-cirrhotics and in patients with complete or incomplete responses to IFN. Frozen sections of biopsies from 5 patie nts were immunostained using antibodies to HLA-DR and B-2-microglobuli n, and positive staining was noted on bile ducts. Before therapy, the %IBD was slightly greater in patients with cirrhosis. After IFN, both %IBD and serum alkaline phosphatase levels decreased in non-cirrhotics who responded to IFN. The change in frequency of IBD with IFN paralle led the changes in the other histological features. No correlation was noted between bile duct inflammation and expression of class I and II antigens. The conclusion is that inflammation of the bile ducts occur s frequently in chronic hepatitis C, correlates with other features of inflammation in the triads, and decreases in response to IFN therapy.