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Technical Briefs |
1
Department of Laboratory Medicine, Osaka University Medical School, Suita 565-0871, Japan, and
2
Kuma Hospital, Kobe 650-0011, Japan;
a author for correspondence: fax 81-6-879-3239, e-mail namino@labo. qjmed.osaka-u.ac.jp
Autoantibodies to the thyrotropin (TSH) receptor (TSHR) are the hallmark of the autoimmune response to the thyroid gland and are responsible for thyrotoxicosis in Graves disease (1). Unlike other autoantibodies, there is no direct assay for TSHR antibodies. Instead, these antibodies are detected either by their ability to inhibit binding of radiolabeled TSH to receptors or by a bioassay of TSHR activation (2)(3). The most widely used assay is a radioreceptor assay, which uses solubilized porcine TSHR, in which the antibody is called TSH-binding inhibitory immunoglobulin (TBII). Serum TBII is easily assayed with a commercially available kit; however, 510% of patients with Graves disease show a negative reaction perhaps related to inadequacies of the assay (4).
Addition of polyethylene glycol (PEG) enhances cAMP production induced
by a patient's IgG, but not by TSH, forskolin, or GTP
S in an in
vitro bioassay for thyroid stimulators (5), suggesting that
the enhancement occurs at the step of antibody-receptor interaction.
Acknowledgments
References
The following articles in journals at HighWire Press have cited this article:
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N. Amino, H. Tada, and Y. Hidaka Screening for Postpartum Thyroid Dysfunction in the General Population Is Beneficial J. Clin. Endocrinol. Metab., June 1, 1999; 84(6): 1813 - 1816. [Full Text] |
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