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Polyethylene Glycol Increases the Detection of Anti-Thyrotropin Receptor Antibodies by a Radioreceptor Assay
Author(s) -
Y. Watanabe,
Hisato Tada,
Yoh Hidaka,
Toru Takano,
Keiko Takeoka,
Shuji Fukata,
Kanji Kuma,
Nobuyuki Amino
Publication year - 1999
Publication title -
clinical chemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.705
H-Index - 218
eISSN - 1530-8561
pISSN - 0009-9147
DOI - 10.1093/clinchem/45.3.407
Subject(s) - thyrotropin receptor , autoantibody , antibody , endocrinology , medicine , receptor , bioassay , chemistry , ligand binding assay , polyethylene glycol , radioligand assay , anti thyroid autoantibodies , graves' disease , thyroid , immunology , biology , biochemistry , genetics
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, 5–10% 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 GTPγS in an in vitro bioassay for thyroid stimulators (5), suggesting that the enhancement occurs at the step of antibody-receptor interaction. We recently found …

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