To evaluate the histological findings in patients with chronic hepatitis C and autoimmune features, liver tissue specimens from 60 patients were graded under code for individual features and composite patterns that denoted autoimmune, vital, combined autoimmune and viral, and nondiscriminative changes. Portal, interface, and acinar hepatitis in any combination with plasma cell infiltration connoted an autoimmune pattern that was associated with higher serum levels of γ-globulin (2.4 ± 0.2 g/dL vs. 1.7 ± 0.1 g/dL; P = .0003) and immunoglobulin G (2,211 ± 227 mg/dL vs. 1,508 ± 83 mg/dL; P = .001) than patients with other patterns. Patients with the autoimmune pattern also had a greater frequency of cirrhosis (43% vs. 8%; P = .003), higher mean Knodell score (13.2 ± 0.9 vs. 6.8 ± 0.9; P < .0001), and a greater occurrence of high-titer smooth muscle antibodies (SMA) (13% vs. 0%; P = .05) than patients with other histological findings. HLA DR3 also occurred more frequently in these individuals than in other patients (48% vs. 15%; P = .01) and normal subjects (43% vs. 16%; P = .01). Patients with nondiscriminative patterns and interface hepatitis had clinical findings similar to those with autoimmune patterns, except for a lower mean serum level of γ-globulin. We conclude that the composite histological pattern that resembles autoimmune hepatitis is associated with greater immunoreactivity, inflammatory activity, and disease severity than other patterns. Interface hepatitis may be the most important histological finding associated with these clinical manifestations.

A case-control study on hepatitis G virus and hepatocellular carcinoma in Italy / A. Tagger, F. Donato, M.L. Ribero, R. Chiesa, V. Tomasoni, M. Fasola, U. Gelatti, A. Albertini, G. Portera, G. Nardi. - In: HEPATOLOGY. - ISSN 0270-9139. - 26:2(1997), pp. 459-459. ((Intervento presentato al 48. convegno Annual Meeting AASLD tenutosi a Chicago Illinois nel 1997 [10.1002/hep.510260229].

A case-control study on hepatitis G virus and hepatocellular carcinoma in Italy

A. Tagger
Primo
;
M.L. Ribero;
1997

Abstract

To evaluate the histological findings in patients with chronic hepatitis C and autoimmune features, liver tissue specimens from 60 patients were graded under code for individual features and composite patterns that denoted autoimmune, vital, combined autoimmune and viral, and nondiscriminative changes. Portal, interface, and acinar hepatitis in any combination with plasma cell infiltration connoted an autoimmune pattern that was associated with higher serum levels of γ-globulin (2.4 ± 0.2 g/dL vs. 1.7 ± 0.1 g/dL; P = .0003) and immunoglobulin G (2,211 ± 227 mg/dL vs. 1,508 ± 83 mg/dL; P = .001) than patients with other patterns. Patients with the autoimmune pattern also had a greater frequency of cirrhosis (43% vs. 8%; P = .003), higher mean Knodell score (13.2 ± 0.9 vs. 6.8 ± 0.9; P < .0001), and a greater occurrence of high-titer smooth muscle antibodies (SMA) (13% vs. 0%; P = .05) than patients with other histological findings. HLA DR3 also occurred more frequently in these individuals than in other patients (48% vs. 15%; P = .01) and normal subjects (43% vs. 16%; P = .01). Patients with nondiscriminative patterns and interface hepatitis had clinical findings similar to those with autoimmune patterns, except for a lower mean serum level of γ-globulin. We conclude that the composite histological pattern that resembles autoimmune hepatitis is associated with greater immunoreactivity, inflammatory activity, and disease severity than other patterns. Interface hepatitis may be the most important histological finding associated with these clinical manifestations.
English
Settore MED/42 - Igiene Generale e Applicata
Intervento a convegno
Esperti anonimi
1997
26
2
459
459
Pubblicato
Periodico con rilevanza internazionale
Annual Meeting AASLD
Chicago Illinois
1997
48
AASLD
Convegno internazionale
Intervento inviato
info:eu-repo/semantics/article
A case-control study on hepatitis G virus and hepatocellular carcinoma in Italy / A. Tagger, F. Donato, M.L. Ribero, R. Chiesa, V. Tomasoni, M. Fasola, U. Gelatti, A. Albertini, G. Portera, G. Nardi. - In: HEPATOLOGY. - ISSN 0270-9139. - 26:2(1997), pp. 459-459. ((Intervento presentato al 48. convegno Annual Meeting AASLD tenutosi a Chicago Illinois nel 1997 [10.1002/hep.510260229].
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Article (author)
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A. Tagger, F. Donato, M.L. Ribero, R. Chiesa, V. Tomasoni, M. Fasola, U. Gelatti, A. Albertini, G. Portera, G. Nardi
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/2434/199230
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