Detection of autoantibody against carbonic anhydrase II in various liver diseases by enzyme-linked immunosorbent assay using appropriate conditions

被引:14
作者
Hosoda, H
Okawa-Takatsuji, M
Tanaka, A
Uwatoko, S
Aotsuka, S
Hasimoto, N
Ozaki, Y
Ikeda, Y
机构
[1] Tokyo Koseinenkin Hosp, Dept Clin Lab, Shinju Ku, Tokyo 1620821, Japan
[2] Int Med Ctr Japan, Div Clin Immunol Res Inst, Shinju Ku, Tokyo, Japan
[3] Teikyo Univ, Sch Med, Div Internal Med, Tokyo, Japan
[4] Tokyo Teishin Hosp, Div Gastroenterol, Tokyo, Tokyo, Japan
[5] Yamanashi Univ, Sch Med, Dept Clin & Lab Med, Yamanashi, Japan
[6] Tokyo Koseinenkin Hosp, Div Internal Med, Shinju Ku, Tokyo, Japan
关键词
anti-CAII antibodies; anti-M2; antibody; ELISA; autoimmune diseases; autoimmune cholangitis; primary biliary cirrhosis;
D O I
10.1016/j.cccn.2003.10.015
中图分类号
R446 [实验室诊断]; R-33 [实验医学、医学实验];
学科分类号
1001 ;
摘要
Background: Immunoglobulin G autoantibody against carbonic anhydrase (CA) II has been detected in the sera of patients with a variety of autoimmune diseases. Antibody against CAII has also been described as a serological marker for distinguishing between cases of autoimmune cholangitis (AIC) and those of primary biliary cirrhosis (PBC). However, the optimal antibody measurement conditions (enzyme-linked immunosorbent assay: ELISA) have not yet been established. Moreover, we also found that a small amount of an IgG-like material exists in purchased CAII reagents, which causes pseudopositive reactions. Methods: The sera of 96 patients with liver disease were examined for the presence of anti-CAII antibody using antigen (CAII) not containing the IgG-like material as the most suitable measurement conditions. Compared with the anti-CAII antibody prevalence of 3.8% found in normal subjects, a significantly higher seroprevatence of the antibody was detected in patients with PBC (31.0%, P < 0.02), autoimmune hepatitis (AIH) (50.0%, P < 0.01) and chronic viral hepatitis (27.5%, P < 0.01). But, in cases of PBC, no significant correlation was noted between the level of anti-CAII antibody and the presence of anti-mitochondrial antibodies (AMA). Conclusions: While CAII may be a target antigen in autoimmune diseases, the anti-CAII antibody is not likely to be a specific marker of AIC. The optimum measurement conditions for the ELISA for anti-CAII antibody would provide us with valuable information to elucidate the underlying immunological abnormalities in liver diseases. (C) 2004 Elsevier B.V. All rights reserved.
引用
收藏
页码:71 / 81
页数:11
相关论文
共 28 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]  
Andoh A, 2002, INT J MOL MED, V9, P499
[3]   Effect of anti-carbonic anhydrase antibodies on carbonic anhydrases I and II [J].
Botrè, F ;
Botrè, C ;
Podestà, E ;
Podda, M ;
Invernizzi, P .
CLINICAL CHEMISTRY, 2003, 49 (07) :1221-1223
[4]  
Brinton DA, 1996, ANN CLIN LAB SCI, V26, P409
[5]   Are antibodies to carbonic anhydrase II specific for anti-mitochondrial antibody-negative primary biliary cirrhosis? [J].
Comay, D ;
Cauch-Dudek, K ;
Hemphill, D ;
Diamandis, E ;
Wanless, I ;
Heathcote, EJ .
DIGESTIVE DISEASES AND SCIENCES, 2000, 45 (10) :2018-2021
[6]   Antibodies to carbonic anhydrase in endometriosis: Prevalence, specificity, and relationship to clinical and laboratory parameters [J].
DCruz, OJ ;
Wild, RA ;
Haas, GG ;
Reichlin, M .
FERTILITY AND STERILITY, 1996, 66 (04) :547-556
[7]   Elevated serum levels of antibodies to carbonic anhydrase I and II in patients with chronic pancreatitis [J].
Frulloni, L ;
Bovo, P ;
Brunelli, S ;
Vaona, B ;
Di Francesco, V ;
Nishimori, I ;
Cavallini, G .
PANCREAS, 2000, 20 (04) :382-388
[8]   ANTIBODIES TO CARBONIC-ANHYDRASE IN PATIENTS WITH IMMUNE CHOLANGIOPATHIES [J].
GORDON, SC ;
QUATTROCIOCCHILONGE, TM ;
KHAN, BA ;
KODALI, VP ;
CHEN, J ;
SILVERMAN, AL ;
KIECHLE, FL .
GASTROENTEROLOGY, 1995, 108 (06) :1802-1809
[9]  
HAROLD F, 1987, INT J BIOCHEM, V19, P101
[10]  
INAGAKI Y, 1991, Journal of Dermatological Science, V2, P147, DOI 10.1016/0923-1811(91)90060-B