Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
2089433 | Journal of Immunological Methods | 2007 | 9 Pages |
Abstract
Autoimmune (Hashimoto's) thyroiditis is a chronic inflammatory disease which affects >Â 3% of the population and shows an increasing prevalence with increasing age. Anti-thyroid autoantibodies, particularly against thyroperoxidase (also known as thyroid peroxidase or TPO), occur commonly in humans with autoimmune thyroid disease, and assays for anti-TPO autoantibodies are used in clinical diagnosis. In contrast anti-TPO autoantibodies have not been observed in classical mouse models of autoimmune thyroiditis, except in cases where mice were deliberately immunized with TPO. In the past, detection of anti-TPO autoantibodies in mice has relied on an indirect immunofluorescence assay (iIFA) which screens for thyroid follicle membrane staining in frozen sections of mouse thyroid glands. Since recent transgenic mouse models of autoimmune thyroiditis spontaneously develop anti-TPO autoantibodies, an assay other than serial dilution and iIFA would be useful to detect and quantify these autoantibodies. In this paper we describe such an assay, based on the capacity of autoimmune mouse sera to bind to the extracellular domain of mouse TPO which was produced in a radioactively labeled form using a coupled in vitro transcription/translation system. The same approach, using human TPO, could provide a highly sensitive method to detect anti-TPO autoantibodies in humans.
Keywords
IA-2TSHRBATween 20DEPCGADTCAautoantibodiesCPMIAAICAPBS-TSDSNODTPOPBSBSAglutamic acid decarboxylasebovine serum albuminInsulin autoantibodiestrichloroacetic acidHumanIndirect immunofluorescenceEnzyme-linked immunosorbent assayELISAthyroiditisThyroperoxidaseBase pair(s)Total Volumeoptimal cutting temperatureNonobese diabeticdiethylpyrocarbonatesodium dodecylsulphateRadioligand binding assaycounts per minutePhosphate buffered salinethyroid stimulating hormonemurine
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Authors
Sarah L. Hayward, Kunimasa Suzuki, John F. Elliott,