IgA class antineutrophil cytoplasmic antibodies in primary sclerosing cholangitis and autoimmune hepatitis

被引:25
作者
Schwarze, C
Terjung, B
Lilienweiss, P
Beuers, U
Herzog, V
Sauerbruch, I
Spengler, U
机构
[1] Univ Bonn, Dept Internal Med 1, D-53105 Bonn, Germany
[2] Univ Munich, Klinikum Grosshadern, Dept Med 2, D-80539 Munich, Germany
[3] Univ Bonn, Inst Cell Biol, D-5300 Bonn, Germany
关键词
ANCA; IIF; immunoglobulin A; liver disease;
D O I
10.1046/j.1365-2249.2003.02195.x
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Antineutrophil cytoplasmic antibodies (ANCA) of IgG class have been described at high prevalence in autoimmune hepatitis (AIH) and primary sclerosing cholangitis (PSC). Data on IgA class ANCA in these diseases are limited. The aim of this study was to determine the prevalence and fluorescence patterns of IgA class ANCA in AIH and PSC and to examine a relationship between the presence of IgA ANCA and clinical characteristics in these patients. Sera from 35 patients with PSC (21 with concomitant inflammatory bowel disease), 40 patients with AIH and 10 healthy controls were studied. ANCA were detected on ethanol-fixed neutrophils using an indirect immunofluorescence technique. ANCA of the IgA class were found in 20% of sera from patients with PSC and in 50% of AIH sera. The majority of AIH patients with IgA class ANCA showed a 'classical' perinuclear staining pattern, whereas the 'classical' and 'atypical' perinuclear fluorescence patterns were distributed equally in PSC. In sera containing IgG and IgA class ANCA simultaneously, IgG class ANCA showed an 'atypical' pANCA fluorescence pattern whereas IgA class ANCA produced a 'classical' perinuclear staining.,ne presence of IgA class ANCA was not associated with disease-specific clinical characteristics. IgA class ANCA are more frequently detected in sera of patients with AIH than PSC. The diversity of fluorescence patterns points to different target antigens of IgA class ANCA with distinct subcellular localizations.
引用
收藏
页码:283 / 289
页数:7
相关论文
共 42 条
[31]   High mobility group (HMG) non-histone chromosomal proteins HMG1 and HMG2 are significant target antigens of perinuclear anti-neutrophil cytoplasmic antibodies in autoimmune hepatitis [J].
Sobajima, J ;
Ozaki, S ;
Uesugi, H ;
Osakada, F ;
Inoue, M ;
Fukuda, Y ;
Shirakawa, H ;
Yoshida, M ;
Rokuhara, A ;
Imai, H ;
Kiyosawa, K ;
Nakao, K .
GUT, 1999, 44 (06) :867-873
[32]   HIGH-TITER ANTINEUTROPHIL CYTOPLASMIC ANTIBODIES IN TYPE-1 AUTOIMMUNE HEPATITIS [J].
TARGAN, SR ;
LANDERS, C ;
VIDRICH, A ;
CZAJA, AJ .
GASTROENTEROLOGY, 1995, 108 (04) :1159-1166
[33]  
TARGAN SR, 1995, J IMMUNOL, V155, P3262
[34]   Atypical antineutrophil cytoplasmic antibodies with perinuclear fluorescence in chronic inflammatory bowel diseases and hepatobiliary disorders colocalize with nuclear lamina proteins [J].
Terjung, B ;
Herzog, V ;
Worman, HJ ;
Gestmann, I ;
Bauer, C ;
Sauerbruch, T ;
Spengler, U .
HEPATOLOGY, 1998, 28 (02) :332-340
[35]   Differentiation of antineutrophil nuclear antibodies in inflammatory bowel and autoimmune liver diseases from antineutrophil cytoplasmic antibodies (p-ANCA) using immunofluorescence microscopy [J].
Terjung, B ;
Worman, HJ ;
Herzog, V ;
Sauerbruch, T ;
Spengler, U .
CLINICAL AND EXPERIMENTAL IMMUNOLOGY, 2001, 126 (01) :37-46
[36]   Atypical p-ANCA in IBD and hepatobiliary disorders react with a 50-kilodalton nuclear envelope protein of neutrophils and myeloid cell lines [J].
Terjung, B ;
Spengler, U ;
Sauerbruch, T ;
Worman, HJ .
GASTROENTEROLOGY, 2000, 119 (02) :310-322
[37]  
VIERLING J, 1998, PRIMARY SCLEROSING C, P37
[38]   Antineutrophil cytoplasm autoantibodies against bactericidal/permeability-increasing protein in inflammatory bowel disease [J].
Walmsley, RS ;
Zhao, MH ;
Hamilton, MI ;
Brownlee, A ;
Chapman, P ;
Pounder, RE ;
Wakefield, AJ ;
Lockwood, CM .
GUT, 1997, 40 (01) :105-109
[39]  
WIESNER RH, 1998, AUTOIMMUNE LIVER DIS, P381
[40]  
Wiik A, 1989, APMIS Suppl, V6, P12