S. Sulkanen et al., Tissue transglutaminase autoantibody enzyme-linked immunosorbent assay in detecting celiac disease, GASTROENTY, 115(6), 1998, pp. 1322-1328
Background & Aims: Tissue transglutaminase has been reported to be the targ
et for endomysial antibodies in celiac disease. We sought to establish whet
her immunoglobulin (Ig) A class tissue transglutaminase autoantibodies can
be considered specific for celiac disease. Methods: Serum samples from 136
patients with untreated celiac disease (diagnosed according to the criteria
of the European Society for Pediatric Gastroenterology, Hepatology and Nut
rition) and 207 disease controls were studied. Enzyme-linked immunosorbent
assay (ELISA) and Western blots were performed using calcium-treated and un
treated tissue transglutaminase as antigen. Reticulin, endomysial, and mous
e monoclonal tissue transglutaminase antibodies were studied by an indirect
immunofluorescence method and gliadin antibodies with ELISA. Results: The
calcium-activated tissue transglutaminase autoantibody ELISA was highly sen
sitive (129 of 136) and specific (194 of 207) in detecting celiac disease.
The new autoantibody ELISA test correlated well with the endomysial antibod
y test. Tissue transglutaminase autoantibody ELISA showed a clearly better
predictive potential than the IgA class gliadin antibody ELISA. Immunoblots
and ELISA blocking studies showed that calcium is needed for the specific
antigen-antibody reaction to occur. Double immunofluorescence staining in h
uman umbilical cord with sera from patients with celiac disease and with mo
noclonal tissue transglutaminase antibodies showed complete overlap. Conclu
sions: Calcium-activated tissue transglutaminase autoantibody ELISA is high
ly accurate in detecting untreated celiac disease. Tissue transglutaminase
seems to be the target self-antigen for endomysial antibodies.