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This study was undertaken to \ninvestigate whether the tissue distribution of transglutaminase \nis also compatible with reticulin, jejunal, and fibroblast \nautoantibody binding patterns. Methods: Sera from patients with \nand without celiac disease, monoclonal tissue transglutaminase \nantibodies, and sera from mice parenterally immunized against \ncommercially available tissue transglutaminase, transglutaminase \ncomplexed with gliadin, or gliadin were used in indirect \nimmunofluorescence and double-staining studies using both rodent \nand primate tissues as substrates. Also, antibody competition, \naffinity chromatography, and potassium thiocyanate extraction \nstudies were undertaken. Results: Tissue transglutaminase \nantibody binding patterns were identical with the extracellular \nbinding patterns seen with celiac patient sera. Human umbilical \ncord-derived fibroblasts exhibited both cytoplasmic and \nextracellular matrix staining. Double staining with patients' \nsera and tissue transglutaminase antibodies showed complete \noverlapping. Tissue transglutaminase effectively absorbed \nreticulin-endomysial antibodies from celiac sera, and patients' \nsera blocked the staining of the monoclonal tissue \ntransglutaminase antibodies. Potassium thiocyanate extraction \nabolished the staining patterns, but they were elicited again \nafter readdition of tissue transglutaminase, Conclusions: \nReticulin, endomysial, and jejunal antibodies detect \ntransglutaminase in both rodent and primate tissues, indicating \nthat these tissue autoantibodies are identical.", "subjects" : [ { "otype" : "Classification", "mtid" : 12347, "link" : "/api/classification/12347", "label" : "Egészségtudományok", "published" : true, "snippet" : true }, { "otype" : "Classification", "mtid" : 12215, "link" : "/api/classification/12215", "label" : "Klinikai orvostan", "published" : true, "snippet" : true } ], "digital" : null, "printed" : null, "sourceYear" : 2007, "foreignEdition" : true, "foreignLanguage" : true, "fullPublication" : true, "conferencePublication" : false, "nationalOrigin" : null, "missingAuthor" : false, "oaType" : "NONE", "oaCheckDate" : "2024-02-14", "oaFree" : false, "citationCount" : 47, "citationCountUnpublished" : 0, 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