Alcohol dehydrogenase: A target of humoral autoimmune response in liver disease

被引:28
作者
Ma, Y
Gaken, J
McFarlane, BM
Foss, Y
Farzaneh, F
McFarlane, IG
MieliVergani, G
Vergani, D
机构
[1] UCL, SCH MED, INST HEPATOL, LONDON WC1E 6HX, ENGLAND
[2] UNIV LONDON KINGS COLL, SCH MED & DENT, DEPT IMMUNOL, LONDON WC2R 2LS, ENGLAND
[3] UNIV LONDON KINGS COLL, SCH MED & DENT, DEPT CHILD HLTH, LONDON WC2R 2LS, ENGLAND
[4] UNIV LONDON KINGS COLL, SCH MED & DENT, DEPT MOL MED, LONDON WC2R 2LS, ENGLAND
[5] UNIV LONDON KINGS COLL, SCH MED & DENT, INST LIVER STUDIES, LONDON WC2R 2LS, ENGLAND
关键词
D O I
10.1053/gast.1997.v112.pm9024302
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Background & Aims: Liver-specific membrane lipoprotein (LSP) is a heterogeneous liver preparation that has been widely used to study autoreactivity in liver disease, The aim of this study was to identify autoantigens in LSP, Methods: Guinea pig anti-LSP serum was used to screen a human liver complementary DNA (cDNA) library, Humoral immune responses to isolated potential autoantigens were investigated by immunoblotting in 91 pediatric patients with various liver diseases, 20 adult patients with alcoholic liver disease and 20 with autoimmune thyroid disease, 37 healthy children, and 20 healthy adults, Results: A 1.6-kilobase cDNA insert isolated from the cDNA library was found to encode amino acids 61-374 of the human alcohol dehydrogenase (ADH)-gamma(1), subunit. Antibodies to this or other ADH subunits were found significantly more frequently in autoimmune liver diseases (19 of 39 patients; 49%), Wilson's disease (5 of 13 patients; 38%), and alcoholic liver disease (10 of 20 patients; 50%) than in normal controls (P < 0.0001, P < 0.005, and P < 0.05, respectively) and correlated with disease activity in autoimmune liver disease, Conclusions: ADH has been identified as a new antigenic component of the LSP using a xenogeneic antiserum to immunoprobe a human cDNA liver library and seems to be a target autoantigen in liver disease, This approach may be useful in identifying other potential autoantigens.
引用
收藏
页码:483 / 492
页数:10
相关论文
共 48 条
[1]  
BARTHOLOMAEUS WN, 1987, IMMUNOLOGY, V60, P321
[2]   HUMAN-LIVER ALCOHOL-DEHYDROGENASE .2. THE PRIMARY STRUCTURE OF THE GAMMA-1 PROTEIN CHAIN [J].
BUHLER, R ;
HEMPEL, J ;
KAISER, R ;
DEZALENSKI, C ;
VONWARTBURG, JP ;
JORNVALL, H .
EUROPEAN JOURNAL OF BIOCHEMISTRY, 1984, 145 (03) :447-453
[3]   MOLECULAR-CLONING AND CHARACTERIZATION OF A CDNA FOR THE BETA-SUBUNIT OF HUMAN ALCOHOL-DEHYDROGENASE [J].
DUESTER, G ;
HATFIELD, GW ;
BUHLER, R ;
HEMPEL, J ;
JORNVALL, H ;
SMITH, M .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA-BIOLOGICAL SCIENCES, 1984, 81 (13) :4055-4059
[4]  
EKLUND H, 1982, J BIOL CHEM, V257, P4349
[5]   PRIMARY SCLEROSING CHOLANGITIS IN CHILDHOOD [J].
ELSHABRAWI, M ;
WILKINSON, ML ;
PORTMANN, B ;
MIELIVERGANI, G ;
CHONG, SKF ;
WILLIAMS, R ;
MOWAT, AP .
GASTROENTEROLOGY, 1987, 92 (05) :1226-1235
[6]  
GALMBOS TJ, 1975, ALCOHOLIC LIVER PATH, P97
[7]  
HABETS WJA, 1989, CLIN EXP IMMUNOL, V76, P172
[8]   THE GAMMA-1 AND GAMMA-2 SUBUNITS OF HUMAN-LIVER ALCOHOL-DEHYDROGENASE - CDNA STRUCTURES, 2 AMINO-ACID REPLACEMENTS, AND COMPATIBILITY WITH CHANGES IN THE ENZYMATIC-PROPERTIES [J].
HOOG, JO ;
HEDEN, LO ;
LARSSON, K ;
JORNVALL, H ;
VONBAHRLINDSTROM, H .
EUROPEAN JOURNAL OF BIOCHEMISTRY, 1986, 159 (02) :215-218
[9]   IMPROVED SERODIAGNOSIS OF HEPATITIS-C VIRUS-INFECTION WITH SYNTHETIC PEPTIDE ANTIGEN FROM CAPSID PROTEIN [J].
HOSEIN, B ;
FANG, CT ;
POPOVSKY, MA ;
YE, J ;
ZHANG, ML ;
WANG, CY .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1991, 88 (09) :3647-3651
[10]   3 HUMAN ALCOHOL-DEHYDROGENASE SUBUNITS - CDNA STRUCTURE AND MOLECULAR AND EVOLUTIONARY DIVERGENCE [J].
IKUTA, T ;
SZETO, S ;
YOSHIDA, A .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1986, 83 (03) :634-638