GENETIC PREDISPOSITIONS FOR THE IMMUNOLOGICAL FEATURES OF CHRONIC ACTIVE HEPATITIS

Citation
Aj. Czaja et al., GENETIC PREDISPOSITIONS FOR THE IMMUNOLOGICAL FEATURES OF CHRONIC ACTIVE HEPATITIS, Hepatology, 18(4), 1993, pp. 816-822
Citations number
44
Categorie Soggetti
Gastroenterology & Hepatology
Journal title
ISSN journal
02709139
Volume
18
Issue
4
Year of publication
1993
Pages
816 - 822
Database
ISI
SICI code
0270-9139(1993)18:4<816:GPFTIF>2.0.ZU;2-5
Abstract
To assess the frequency and genetic predispositions of concurrent immu nological diseases and immunoserological markers in autoimmune hepatit is and chronic viral hepatitis, we assessed 185 patients prospectively , including 122 patients with autoimmune hepatitis and 63 patients wit h viral disease. Human leukocyte antigens were determined in all patie nts. Sixty patients (32%) had concurrent immunological diseases, and t he majority of the diseases (68%) had known human leukocyte antigen as sociations. Although patients with autoimmune hepatitis had concurrent immunological diseases more commonly than those with viral disease (3 8% vs. 22%; p = 0.04), the nature of the diseases was similar in both groups, as were the frequencies of human leukocyte antigen-DR4 (42% vs . 39%; p = 0.7). The presence of human leukocyte antigen-DR4 was assoc iated with the concurrence of immunological diseases in both autoimmun e (62% vs. 33%; p = 0.0 1) and viral hepatitis (75% vs. 29%; p = 0.009 ). In autoimmune hepatitis, human leukocyte antigen-DR4 was also assoc iated with the expression of smooth muscle antibodies and high-titer a ntinuclear antibodies. We conclude that concurrent immunological disea ses and immunoserological markers are common in autoimmune and chronic viral hepatitis. Both conditions have a common genetic predisposition for concurrent immunological disease associated with human leukocyte antigen-DR4. The expression of smooth muscle antibodies and high-titer antinuclear antibodies is associated with human leukocyte antigen-DR4 in autoimmune hepatitis only, suggesting that this response is associ ated with triggering antigens and immune recognition systems that are different from those in viral disease.