Characterization and clinical impact of antinuclear antibodies in primary biliary cirrhosis

被引:221
作者
Muratori, P
Muratori, L
Ferrari, R
Cassani, F
Bianchi, G
Lenzi, M
Rodrigo, L
Linares, A
Fuentes, D
Bianchi, FB
机构
[1] Univ Bologna, Policlin S Orsola Malpighi, Dipartimento Med Interna Cardioangiol Epatol, Alma Mater Studiorum, I-40138 Bologna, Italy
[2] Hosp Cent Asturias, Serv Gastroenterol, Oviedo, Spain
关键词
D O I
10.1016/S0002-9270(02)05925-7
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
OBJECTIVES: The clinical impact of antinuclear antibodies in primary biliary cirrhosis is uncertain. We analyzed in detail the antinuclear antibodies reactivity of primary biliary cirrhosis patients and correlated the fine specificities observed with clinical, biochemical, and immunologic parameters. METHODS: A total of 96 consecutive primary biliary cirrhosis patients and 283 pathologic controls were studied. To dissect the fine antinuclear antibodies specificities we used different techniques, such as indirect immunofluorescence on cryostat tissue sections and cell culture (HEp-2 cells), counterimmunoelectrophoresis with thymus and spleen extracts, ELISA assays with recombinant Sp100 and purified gp210 and Lamin B receptor, and immunoblot with several recombinant nuclear and cytoplasmic antigens. RESULTS: Antinuclear antibodies were detected in 53% of patients, with the following hierarchy of specificities: 27% anti-Sp100, 16% "multiple nuclear dots," 16% anti-gp210, 16% anti-centromere, 7% XR1, 6% anti-lamin B receptor, 5% anti-SS-A/Ro, 5% anti-ribonucleoprotein, 4% XR2, 2% anti-SS-B/La, 2% perinuclear antineutrophil cytoplasmic antibodies, and 1% anti-double-stranded deoxyribonucleic acid. Several patients showed multiple specificities. The,''multiple nuclear dots" pattern was detected more often in antimitochondrial antibodies negative patients. In particular, primary biliary cirrhosis specific antinuclear antibodies (anti-Sp100, anti-gp210, and anti-lamin B receptor) were detected in nine of 13 anti mitochondrial negative primary biliary cirrhosis cases. Anti-gp210 was more frequent in patients with more pronounced cholestasis and more impaired liver function. CONCLUSIONS: Antinuclear antibodies reactivities are present in more than half of primary biliary cirrhosis patients and target diverse autoantigens located in distinct subnuclear structures. Anti-gp210 identifies a subgroup of primary biliary cirrhosis patients,with more serious liver disease. Positivity for anti-Sp100, anti-gp210, and anti-lamin B receptor, either alone or in combination, may act as a serologic marker of antimitochondrial antibodies negative primary biliary cirrhosis. (C) 2003 by Am. Coll. of Gastroenterology.
引用
收藏
页码:431 / 437
页数:7
相关论文
共 42 条
[1]   The ability of anti-carbonic anhydrase II antibody to distinguish autoimmune cholangitis from primary biliary cirrhosis in Japanese patients [J].
Akisawa, N ;
Nishimori, I ;
Miyaji, E ;
Iwasaki, S ;
Maeda, T ;
Shimizu, H ;
Sato, N ;
Onishi, S .
JOURNAL OF GASTROENTEROLOGY, 1999, 34 (03) :366-371
[2]   International Autoimmune Hepatitis Group Report:: review of criteria for diagnosis of autoimmune hepatitis [J].
Alvarez, E ;
Berg, PA ;
Bianchi, FB ;
Bianchi, L ;
Burroughs, AK ;
Cancado, EL ;
Chapman, RW ;
Cooksley, WGE ;
Czaja, AJ ;
Desmet, VJ ;
Donaldson, RT ;
Eddleston, ALWF ;
Fainboim, L ;
Heathcote, J ;
Homberg, JC ;
Hoofnagle, JH ;
Kakumu, S ;
Krawitt, EL ;
Mackay, IR ;
MacSween, RNM ;
Maddrey, WC ;
Manns, MP ;
McFarlane, IG ;
zum Büschenfelde, KHM ;
Mieli-Vergani, G ;
Nakanuma, Y ;
Nishioka, M ;
Penner, E ;
Porta, G ;
Portmann, BC ;
Reed, WD ;
Rodes, J ;
Schalm, SW ;
Scheuer, PJ ;
Schrumpf, E ;
Seki, T ;
Toda, G ;
Tsuji, T ;
Tygstrup, N ;
Vergani, D ;
Zeniya, M .
JOURNAL OF HEPATOLOGY, 1999, 31 (05) :929-938
[3]  
Bandin O, 1996, HEPATOLOGY, V23, P1020
[4]   AUTOIMMUNE CHOLANGIOPATHY - PART OF THE SPECTRUM OF AUTOIMMUNE CHRONIC ACTIVE HEPATITIS [J].
BENARI, Z ;
DHILLON, AP ;
SHERLOCK, S .
HEPATOLOGY, 1993, 18 (01) :10-15
[5]  
BERNSTEIN RM, 1984, CLIN EXP IMMUNOL, V55, P553
[6]   IDENTIFICATION OF ANTIBODIES TO ACIDIC ANTIGENS BY COUNTERIMMUNOELECTROPHORESIS [J].
BERNSTEIN, RM ;
BUNN, CC ;
HUGHES, GRV .
ANNALS OF THE RHEUMATIC DISEASES, 1982, 41 (05) :554-555
[7]   CLASSIFICATION OF SMOOTH-MUSCLE AUTOANTIBODIES DETECTED BY IMMUNOFLUORESCENCE [J].
BOTTAZZO, GF ;
FLORINCHRISTENSEN, A ;
FAIRFAX, A ;
SWANA, G ;
DONIACH, D ;
GROESCHELSTEWART, U .
JOURNAL OF CLINICAL PATHOLOGY, 1976, 29 (05) :403-410
[8]  
CASSANI F, 1987, CLIN EXP IMMUNOL, V68, P588
[9]   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
[10]   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