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.
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页码:31 / 34
页数:4
相关论文
共 19 条
[11]  
Rostami K, 1999, AM J GASTROENTEROL, V94, P888
[12]  
Sárdy M, 1999, CLIN CHEM, V45, P2142
[13]   Antibodies to human recombinant tissue transglutaminase measured by radioligand assay: Evidence for high diagnostic sensitivity for celiac disease [J].
Seissler, J ;
Boms, S ;
Wohlrab, U ;
Morgenthaler, NG ;
Mothes, T ;
Boehm, BO ;
Scherbaum, WA .
HORMONE AND METABOLIC RESEARCH, 1999, 31 (06) :375-379
[14]   New tool to predict celiac disease on its way to the clinics [J].
Sollid, LM ;
Scott, H .
GASTROENTEROLOGY, 1998, 115 (06) :1584-1586
[15]   Comparative evaluation of serologic tests for celiac disease: A European initiative toward standardization [J].
Stern, M .
JOURNAL OF PEDIATRIC GASTROENTEROLOGY AND NUTRITION, 2000, 31 (05) :513-519
[16]   Tissue transglutaminase autoantibody enzyme-linked immunosorbent assay in detecting celiac disease [J].
Sulkanen, S ;
Halttunen, T ;
Laurila, A ;
Kolho, KL ;
Korponay-Szabó, IR ;
Sarnesto, A ;
Savilahti, E ;
Collin, P ;
Mäki, M .
GASTROENTEROLOGY, 1998, 115 (06) :1322-1328
[17]   Diagnosis of celiac sprue [J].
Trier, JS .
GASTROENTEROLOGY, 1998, 115 (01) :211-216
[18]   IgA antibodies to tissue transglutaminase: An effective diagnostic test for celiac disease [J].
Troncone, R ;
Maurano, F ;
Rossi, M ;
Micillo, M ;
Greco, L ;
Auricchio, R ;
Salerno, G ;
Salvatore, F ;
Sacchetti, L .
JOURNAL OF PEDIATRICS, 1999, 134 (02) :166-171
[19]   Antibodies to gliadin, endomysium, and tissue transglutaminase for the diagnosis of celiac disease [J].
Vitoria, JC ;
Arrieta, A ;
Arranz, C ;
Ayesta, A ;
Sojo, A ;
Maruri, N ;
García-Masdevall, MD .
JOURNAL OF PEDIATRIC GASTROENTEROLOGY AND NUTRITION, 1999, 29 (05) :571-574