Antitissue transglutaminase antibodies outside celiac disease

被引:61
作者
Clemente, MG [1 ]
Musu, MP [1 ]
Frau, F [1 ]
Lucia, C [1 ]
De Virgiliis, S [1 ]
机构
[1] Univ Cagliari, Dipartimento Sci Biomed & Biotecnol, Pediat Clin 2, Ctr Reg Microcitemie, I-09121 Cagliari, Italy
关键词
autoantibody; tissue transglutaminase; celiac disease; autoimmune liver disease;
D O I
10.1097/00005176-200201000-00008
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Background: Tissue transglutaminase enzyme-linked immunosorbent assay (tTG-ELISA) has recently been proposed as a simple and fast screening test for celiac disease (CD). The rate of false-positive and false-negative tests with tTG-ELISA, however, has not been definitively established. Therefore, the aim of our study was to investigate anti-tTG antibodies (TGA) not only in untreated patients with CD and in healthy controls, but also in a large group of patients with other autoimmune diseases. Methods: The presence of TGA was investigated in sera from I I I patients with untreated CD, 96 patients with other autoimmune conditions (28 with autoimmune liver disease, 46 with insulin-dependent diabetes mellitus, 10 with inflammatory bowel syndrome, 12 with type I polyglandular syndrome) and from 100 healthy controls using guinea pic, tTG-ELISA (gp-TG/ELISA) and highly purified recombinant human tTG-ELISA (h-TG/ELISA). Western blotting with guinea pig tTG was also performed. Results: Ninety-four patients with CD who tested positive for antiendomysial antibodies (AEA) and one who tested negative for AEA showed antibodies against the gp-TG, Among the controls, 50% of patients with autoimmune liver disease and 6.5% of patients with insulin-dependent diabetes mellitus tested positive with gp-TG/ELISA. Western blotting experiments revealed that the high rate of positive tests observed using ELISA among the control group sera is attributable to impurities in the op-TG preparation. However, h-TG/ELISA tests were positive for the sera from all patients who tested positive for AEA and from one control who tested negative for AEA, whereas h-TG/ELISA tests were negative for all CD patients who tested negative for AEA and for other controls who tested negative for AEA. Conclusions: The frequency of false-negative and false-positive tests represents the major limit to the use of gp-TG/ELISA. However, because h-TG/ELISA is both simple and fast, it could be used in large screening programs for CD.
引用
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页码:31 / 34
页数:4
相关论文
共 19 条
[1]   One third of HLA DQ2 homozygous patients with type 1 diabetes express celiac disease-associated transglutaminase autoantibodies [J].
Bao, F ;
Yu, LP ;
Babu, S ;
Wang, TB ;
Hoffenberg, EJ ;
Rewers, M ;
Eisenbarth, GS .
JOURNAL OF AUTOIMMUNITY, 1999, 13 (01) :143-148
[2]   Comparison of tissue transglutaminase-specific antibody assays with established antibody measurements for coeliac disease [J].
Bazzigaluppi, E ;
Lampasona, V ;
Barera, G ;
Venerando, A ;
Bianchi, C ;
Chiumello, G ;
Bonifacio, E ;
Bosi, E .
JOURNAL OF AUTOIMMUNITY, 1999, 12 (01) :51-56
[3]  
Biagi F, 1999, AM J GASTROENTEROL, V94, P2187
[4]   ANTIGLIADIN AND ANTIENDOMYSIUM ANTIBODY DETERMINATION FOR CELIAC-DISEASE [J].
BURGINWOLFF, A ;
GAZE, H ;
HADZISELIMOVIC, F ;
HUBER, H ;
LENTZE, MJ ;
NUSSLE, D ;
REYMONDBERTHET, C .
ARCHIVES OF DISEASE IN CHILDHOOD, 1991, 66 (08) :941-947
[5]   Immune reaction against the cytoskeleton in coeliac disease [J].
Clemente, MG ;
Musu, MP ;
Frau, F ;
Brusco, G ;
Sole, G ;
Corazza, GR ;
De Virgiliis, S .
GUT, 2000, 47 (04) :520-526
[6]   Autoantibodies to tissue transglutaminase as predictors of celiac disease [J].
Dieterich, W ;
Laag, E ;
Schöpper, H ;
Volta, U ;
Ferguson, A ;
Gillett, H ;
Riecken, EO ;
Schuppan, D .
GASTROENTEROLOGY, 1998, 115 (06) :1317-1321
[7]   Identification of tissue transglutaminase as the autoantigen of celiac disease [J].
Dieterich, W ;
Ehnis, T ;
Bauer, M ;
Donner, P ;
Volta, U ;
Riecken, EO ;
Schuppan, D .
NATURE MEDICINE, 1997, 3 (07) :797-801
[8]  
Koop I, 2000, AM J GASTROENTEROL, V95, P2009
[9]   IgA anti-tissue transglutaminase as a diagnostic marker of gluten sensitive enteropathy [J].
Lock, RJ ;
Pitcher, MCL ;
Unsworth, DJ .
JOURNAL OF CLINICAL PATHOLOGY, 1999, 52 (04) :274-277
[10]   Coeliac disease [J].
Maki, M ;
Collin, P .
LANCET, 1997, 349 (9067) :1755-1759