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- Dahlbom, I (författare)
Immunoglobulin g (IgG) anti-tissue transglutaminase antibodies used as markers for IgA-deficient celiac disease patients
- Artikel/kapitelEngelska2005
Förlag, utgivningsår, omfång ...
- 2005
Nummerbeteckningar
- LIBRIS-ID:oai:lup.lub.lu.se:8f8e2674-3da6-4ade-ab5b-3dafe20d94ed
- https://lup.lub.lu.se/record/229350URI
- https://doi.org/10.1128/CDLI.12.2.254-258.2005DOI
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- Språk:engelska
- Sammanfattning på:engelska
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- SwePubSwePub
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- The role of immunoglobulin A (IgA) anti-tissue transglutaminase antibodies (IgA-tTG) as predictors of untreated celiac disease (CoD) is well documented, and the presence and levels of these antibodies are most accurately monitored with native or recombinant human antigens. However, IgA-deficient CoD patients are not identified by IgA serology, and conflicting results concerning the diagnostic validity of IgG antibodies against gliadin (IgG-AGA), endomysium (IgG-EmA), and tTG (IgG-tTG) have been reported. The aim of the present study was to evaluate the utility of IgG-tTG for the detection of CoD in IgA-deficient patients. Samples from 115 IgA-deficient and 200 IgA-sufficient subjects were collected and tested for the presence of IgA and IgG antibodies against tTG, EmA, and AGA. Antibodies against tTG were measured by an enzyme-linked immunosorbent assay based on recombinant human tTG, and antibodies against EmA were determined by immunofluorescence. The values for IgG-tTG showed a higher correlation (correlation coefficient [r] = 0.91) with those for IgG-EmA for the IgA-deficient subjects than for the IgA-sufficient subjects (r = 0.88). The overall concordance of the positive and negative results between IgG-tTG and IgG-EmA was 97%, and the IgG-tTG assay discriminated between IgG-EmA-positive and -negative subjects with IgA deficiency at a rate of 100%. Elevated levels of IgG-tTG and IgG-EmA were measured in 70% of the IgA-sufficient subjects. IgG-tTG detection with recombinant human tTG is a good alternative to IgG-EmA detection, and the addition of IgG-tTG assessment to present screening methods may improve the ability to identify IgA-deficient subjects with CoD.
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Biuppslag (personer, institutioner, konferenser, titlar ...)
- Olsson, M (författare)
- Forooz, NK (författare)
- Sjoholm, AG (författare)
- Truedsson, LennartLund University,Lunds universitet,Avdelningen för mikrobiologi, immunologi och glykobiologi - MIG,Institutionen för laboratoriemedicin,Medicinska fakulteten,Division of Microbiology, Immunology and Glycobiology - MIG,Department of Laboratory Medicine,Faculty of Medicine(Swepub:lu)mmb-ltr (författare)
- Hansson, T (författare)
- Avdelningen för mikrobiologi, immunologi och glykobiologi - MIGInstitutionen för laboratoriemedicin (creator_code:org_t)
Sammanhörande titlar
- Ingår i:Clinical and Diagnostic Laboratory Immunology12:2, s. 254-2581071-412X
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- Clinical and Diagnostic Laboratory Immunology (Sök värdpublikationen i LIBRIS)
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- Dahlbom, I
- Olsson, M
- Forooz, NK
- Sjoholm, AG
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- Hansson, T
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