Autoantibodies to tissue transglutaminase as predictors of celiac disease

被引:492
作者
Dieterich, W
Laag, E
Schöpper, H
Volta, U
Ferguson, A
Gillett, H
Riecken, EO
Schuppan, D
机构
[1] Univ Erlangen Nurnberg, Med Klin 1, D-91054 Erlangen, Germany
[2] Free Univ Berlin, Klinikum Benjamin Franklin, Dept Gastroenterol, D-12200 Berlin, Germany
[3] Univ Bologna, Policlin S Orsola, Dept Internal Med Cardioangiol & Hepatol, I-40138 Bologna, Italy
[4] Univ Edinburgh, Western Gen Hosp, Dept Med, Edinburgh EH4 2XU, Midlothian, Scotland
关键词
D O I
10.1016/S0016-5085(98)70007-1
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Backguound & Aims: Immunoglobulin A (IgA) autoantibodies to endomysium (EMA) are highly specific and sensitive markers for celiac disease. Recently, we identified tissue transglutaminase (tTG) as the major if not sole endomysial autoantigen. Methods: An enzyme-linked immunosorbent assay (ELISA) was established to measure IgA anti-tTG titers in serum samples from 106 celiac patients with partial or subtotal villous atrophy, 43 celiac patients on a gluten-free diet, and 114 diseased and healthy controls. Results were correlated with clinical and histological data and with EMA titers. Results: In patients with biopsy-proven celiac disease consuming a normal, gluten-containing diet, 98.1% of the serum samples had elevated IgA titers against tTG, whereas 94.7% of the control sera were negative. IgA anti-tTG correlated positively with semiquantitative IgA EMA titers (r = 0.862; P < 0.0001). Conclusions: An ELISA based on tTG allows diagnosis of celiac disease with a high sensitivity and specificity. IgA anti-tTG and IgA EMA show an excellent correlation, further confirming the enzyme as the celiac disease autoantigen. Because the assay is quantitative, not subjected to interobserver variation, and easy to perform, it will be a useful tool for population screening of a hitherto underdiagnosed disease.
引用
收藏
页码:1317 / 1321
页数:5
相关论文
共 22 条
  • [1] BOWNESS JM, 1987, J BIOL CHEM, V262, P1022
  • [2] ANTIGLIADIN AND ANTIENDOMYSIUM ANTIBODY DETERMINATION FOR CELIAC-DISEASE
    BURGINWOLFF, A
    GAZE, H
    HADZISELIMOVIC, F
    HUBER, H
    LENTZE, MJ
    NUSSLE, D
    REYMONDBERTHET, C
    [J]. ARCHIVES OF DISEASE IN CHILDHOOD, 1991, 66 (08) : 941 - 947
  • [3] CELIAC-DISEASE IN THE YEAR 2000 - EXPLORING THE ICEBERG
    CATASSI, C
    RATSCH, IM
    FABIANI, E
    ROSSINI, M
    BORDICCHIA, F
    CANDELA, F
    COPPA, GV
    GIORGI, PL
    [J]. LANCET, 1994, 343 (8891) : 200 - 203
  • [4] SEROLOGICAL SCREENING OF CELIAC-DISEASE - CHOOSING THE OPTIMAL PROCEDURE ACCORDING TO VARIOUS PREVALENCE VALUES
    CORRAO, G
    CORAZZA, GR
    ANDREANI, ML
    TORCHIO, P
    VALENTINI, RA
    GALATOLA, G
    QUAGLINO, D
    GASBARRINI, G
    DIORIO, F
    [J]. GUT, 1994, 35 (06) : 771 - 775
  • [5] Identification of tissue transglutaminase as the autoantigen of celiac disease
    Dieterich, W
    Ehnis, T
    Bauer, M
    Donner, P
    Volta, U
    Riecken, EO
    Schuppan, D
    [J]. NATURE MEDICINE, 1997, 3 (07) : 797 - 801
  • [6] Fibroblasts and transforming growth factor beta induce organization and differentiation of T84 human epithelial
    Halttunen, T
    Marttinen, A
    Rantala, I
    Kainulainen, H
    Maki, M
    [J]. GASTROENTEROLOGY, 1996, 111 (05) : 1252 - 1262
  • [7] REQUIREMENT FOR TRANSGLUTAMINASE IN THE ACTIVATION OF LATENT TRANSFORMING GROWTH-FACTOR-BETA IN BOVINE ENDOTHELIAL-CELLS
    KOJIMA, S
    NARA, K
    RIFKIN, DB
    [J]. JOURNAL OF CELL BIOLOGY, 1993, 121 (02) : 439 - 448
  • [8] ENDOMYSIUM ANTIBODIES IN CELIAC-DISEASE - AN IMPROVED METHOD
    LADINSER, B
    ROSSIPAL, E
    PITTSCHIELER, K
    [J]. GUT, 1994, 35 (06) : 776 - 778
  • [9] Lankisch PG, 1996, Z GASTROENTEROL, V34, P473
  • [10] TRANSFORMING GROWTH-FACTORS AND THE REGULATION OF CELL-PROLIFERATION
    LYONS, RM
    MOSES, HL
    [J]. EUROPEAN JOURNAL OF BIOCHEMISTRY, 1990, 187 (03): : 467 - 473