Isolation of antigens recognized by coeliac disease autoantibodies and their use in enzyme immunoassay of endomysium and reticulin antibody-positive human sera

被引:16
作者
Borner, H [1 ]
Osman, AA [1 ]
Meergans, T [1 ]
Weiske, T [1 ]
Mothes, T [1 ]
机构
[1] UNIV LEIPZIG,INST CLIN CHEM & PATHOBIOCHEM,D-04103 LEIPZIG,GERMANY
关键词
endomysium antibodies; reticulin antibodies; gliadin antibodies; coeliac disease; autoantigens;
D O I
10.1046/j.1365-2249.1996.d01-850.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
Components were isolated from rat liver, sheep lung, rhesus and orang-utan intestine. In enzyme immunoassay, these components detected 57%, 72%, 84% and 88% of human sera containing endomysium and reticulin antibodies (EmA and ARA). At most, 7% of EmA/ARA-negative sera reacted with the antigens. The spectrum of EmA/ARA-positive sera reactive with the various components was different but overlapping. When the antigens of sheep lung and orang-utan intestine were used as a cocktail, 98% of EmA/ARA-positive sera (45/46), but only 2% of control sera (1/46) were detected. The isolated antigens from sheep lung and monkey intestines were able to absorb EmA and ARA from human sera and thus should be suspected to contain the epitopes recognized by EmA and ARA, whereas the rat liver component did not bind. Therefore, the spectrum of autoantibodies in coeliac disease might comprise more than that covered by the terms EmA and ARA. The N-terminal amino acid sequence of some of the antigens was homologous with casein, gliadin, fibrinogen, and collagen.
引用
收藏
页码:344 / 350
页数:7
相关论文
共 27 条
[11]   COPPER STAINING - A 5-MINUTE PROTEIN STAIN FOR SODIUM DODECYL-SULFATE POLYACRYLAMIDE GELS [J].
LEE, C ;
LEVIN, A ;
BRANTON, D .
ANALYTICAL BIOCHEMISTRY, 1987, 166 (02) :308-312
[12]   CHARACTERIZATION OF MUSCLE EPIMYSIUM, PERIMYSIUM AND ENDOMYSIUM COLLAGENS [J].
LIGHT, N ;
CHAMPION, AE .
BIOCHEMICAL JOURNAL, 1984, 219 (03) :1017-1026
[13]   EVALUATION OF A SERUM IGA-CLASS RETICULIN ANTIBODY-TEST FOR THE DETECTION OF CHILDHOOD CELIAC-DISEASE [J].
MAKI, M ;
HALLSTROM, O ;
VESIKARI, T ;
VISAKORPI, JK .
JOURNAL OF PEDIATRICS, 1984, 105 (06) :901-905
[14]   REACTION OF HUMAN NONCOLLAGENOUS POLYPEPTIDES WITH CELIAC-DISEASE AUTOANTIBODIES [J].
MAKI, M ;
HALLSTROM, O ;
MARTTINEN, A .
LANCET, 1991, 338 (8769) :724-725
[15]  
MAKI M, 1992, GLUTEN SENSITIVE ENT, P108
[16]   PURIFICATION OF FIBROBLAST-DERIVED CELIAC-DISEASE AUTOANTIGEN MOLECULES [J].
MARTTINEN, A ;
MAKI, M .
PEDIATRIC RESEARCH, 1993, 34 (04) :420-423
[17]   INVESTIGATION OF GLIADIN BINDING TO DIFFERENT SELECTED PROTEINS USING A BIOTIN-STREPTAVIDIN SYSTEM [J].
OSMAN, AA ;
BRAUNERSREUTHER, I ;
MOTHES, T .
ZEITSCHRIFT FUR LEBENSMITTEL-UNTERSUCHUNG UND-FORSCHUNG, 1994, 198 (03) :249-252
[18]  
PRAS M, 1973, BRIT J EXP PATHOL, V54, P449
[19]  
PRAS M, 1974, IMMUNOLOGY, V27, P469
[20]  
SCOTT DL, 1986, IRCS MED SCI-BIOCHEM, V14, P254