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Binding assay for thyrotropin receptor autoantibodies using the recombinant receptor protein.

Authors :
Costagliola, Sabine
Swillens, Stéphane
Niccoli, P
Dumont, Jacques
Vassart, Gilbert
Ludgate, Marian
Costagliola, Sabine
Swillens, Stéphane
Niccoli, P
Dumont, Jacques
Vassart, Gilbert
Ludgate, Marian
Source :
The Journal of clinical endocrinology and metabolism, 75 (6
Publication Year :
1992

Abstract

We have characterized a transfected Chinese hamster ovary cell line, JP09, which expresses high levels of the human TSH receptor (TSH-R). Based on a theoretical biological activity for TSH of 40 IU/mg, JP09 has approximately 90,000 receptors per cell, having a dissociation constant of 1.64 x 10(3) mU/L or 1.47 x 10(-9) mol/L. We have used JP09 to prepare solubilized TSH-Rs which have formed the basis of a binding assay for thyroid-binding inhibiting immunoglobulins in unfractionated sera. We have compared the JP09 assay with the TRAK assay (which is based on solubilized porcine TSH-R) and found a highly positive correlation between the two assays, r = 0.83 P < 0.0001, in 55 sera from patients with autoimmune thyroid disease. JP09 can be adapted to growth in suspension culture, permitting large scale production. The tracer in the assay is bovine [125I]TSH; surprisingly, despite the use of a hTSH-R, hTSH had no effect on the binding of the tracer up to 10(3) mU/L and only a minor effect at 10(4) mU/L.<br />Comparative Study<br />Journal Article<br />info:eu-repo/semantics/published

Details

Database :
OAIster
Journal :
The Journal of clinical endocrinology and metabolism, 75 (6
Notes :
No full-text files, English
Publication Type :
Electronic Resource
Accession number :
edsoai.ocn764602842
Document Type :
Electronic Resource