Autoantibodies against a 210 kDa glycoprotein of the nuclear pore complex as a prognostic marker in patients with primary biliary cirrhosis

被引:88
作者
Itoh, S
Ichida, T
Yoshida, T
Hayakawa, A
Uchida, M
Tashiro-Itoh, T
Matsuda, Y
Ishihara, K
Asakura, H
机构
[1] Niigata Univ, Sch Med, Dept Internal Med 3, Niigata 951, Japan
[2] Niigata Univ, Coll Biomed Technol, Niigata 951, Japan
关键词
anti-gp210; antibody; primary biliary cirrhosis; prognostic marker;
D O I
10.1111/j.1440-1746.1998.01553.x
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
It has been reported that the presence of anti-nuclear antibody against a 210 kDa glycoprotein of nuclear pore complex (anti-gp210) is highly specific for primary biliary cirrhosis (PBC). The aim of the present study was to investigate the significance of anti-gp210, especially as a prognostic marker. The presence of anti-gp210 was ascertained in 113 patients with PBC and 162 controls by indirect immunofluorescence assay using HepG2. cells and immunoblotting analysis using nuclear extracts from HeLa cells. Anti-gp210 was detected in 25 of the 113 (22.1%) patients. None of the 162 controls was positive for anti-gp210. The appearance and titre of anti-gp210 in the patients with PBC did not vary from the time of diagnosis and through their clinical course. Anti-mitochondrial antibodies (AMA), including antibodies against pyruvate dehydrogenase complex, branched chain a-ketoacid dehydrogenase complex and or-ketoglutarate dehydrogenase complex, were not detected by enzyme-linked immunosorbent assay in five of the 113 (4.4%) patients with PBC. However, anti-gp210 alone was positive in one of these five patients. The difference in prognosis was statistically significant; patients with PBC positive for anti-gp210 died from hepatic failure more frequently than those who were negative (P < 0.01), although there were no statistically significant differences in the frequency of jaundice and the histological stage at the time of diagnosis between the two groups. We suggest that the presence of anti-gp210 is one of the independent prognostic markers able to predict, at the time of diagnosis, a poor outcome in patients with PBC.
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页码:257 / 265
页数:9
相关论文
共 44 条
[1]   AUTOIMMUNE CHOLANGIOPATHY - PART OF THE SPECTRUM OF AUTOIMMUNE CHRONIC ACTIVE HEPATITIS [J].
BENARI, Z ;
DHILLON, AP ;
SHERLOCK, S .
HEPATOLOGY, 1993, 18 (01) :10-15
[2]  
BERG PA, 1982, LANCET, V2, P1423
[3]   ANTIMITOCHONDRIAL ANTIBODIES IN PRIMARY BILIARY-CIRRHOSIS [J].
BERG, PA ;
KLEIN, R ;
LINDENBORNFOTINOS, J .
JOURNAL OF HEPATOLOGY, 1986, 2 (01) :123-131
[4]   PRIMARY STRUCTURE OF THE HUMAN M2 MITOCHONDRIAL AUTO-ANTIGEN OF PRIMARY BILIARY-CIRRHOSIS - DIHYDROLIPOAMIDE ACETYLTRANSFERASE [J].
COPPEL, RL ;
MCNEILAGE, LJ ;
SURH, CD ;
VANDEWATER, J ;
SPITHILL, TW ;
WHITTINGHAM, S ;
GERSHWIN, ME .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1988, 85 (19) :7317-7321
[5]   THE 210-KD NUCLEAR-ENVELOPE POLYPEPTIDE RECOGNIZED BY HUMAN AUTOANTIBODIES IN PRIMARY BILIARY-CIRRHOSIS IS THE MAJOR GLYCOPROTEIN OF THE NUCLEAR-PORE [J].
COURVALIN, JC ;
LASSOUED, K ;
BARTNIK, E ;
BLOBEL, G ;
WOZNIAK, RW .
JOURNAL OF CLINICAL INVESTIGATION, 1990, 86 (01) :279-285
[6]   IDENTIFICATION AND CHARACTERIZATION OF AUTOANTIBODIES AGAINST THE NUCLEAR-ENVELOPE LAMIN-B RECEPTOR FROM PATIENTS WITH PRIMARY BILIARY-CIRRHOSIS [J].
COURVALIN, JC ;
LASSOUED, K ;
WORMAN, HJ ;
BLOBEL, G .
JOURNAL OF EXPERIMENTAL MEDICINE, 1990, 172 (03) :961-967
[7]   IDENTIFICATION AND CHARACTERIZATION OF A NUCLEAR-PORE COMPLEX PROTEIN [J].
DAVIS, LI ;
BLOBEL, G .
CELL, 1986, 45 (05) :699-709
[8]   ACCURATE TRANSCRIPTION INITIATION BY RNA POLYMERASE-II IN A SOLUBLE EXTRACT FROM ISOLATED MAMMALIAN NUCLEI [J].
DIGNAM, JD ;
LEBOVITZ, RM ;
ROEDER, RG .
NUCLEIC ACIDS RESEARCH, 1983, 11 (05) :1475-1489
[9]  
DINGWALL C, 1986, ANNU REV CELL BIOL, V2, P367, DOI 10.1146/annurev.cellbio.2.1.367
[10]  
Engvall E, 1980, Methods Enzymol, V70, P419