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RESEARCH PRODUCT

Comparison of a Bridge Immunoassay with Two Bioassays for Thyrotropin Receptor Antibody Detection and Differentiation

Derik HermsenMatthias SchottStephanie AlleleinGeorge J. KahalyMichael KanitzMargret EhlersTanja Diana

subject

MaleGoiterendocrine system diseasesEndocrinology Diabetes and MetabolismClinical Biochemistry030204 cardiovascular system & hematologyBiochemistryThyroiditis0302 clinical medicineEndocrinologyEuthyroidThyroid cancerAged 80 and overImmunoassaybiologymedicine.diagnostic_testThyroidCell DifferentiationReceptors ThyrotropinGeneral MedicineMiddle AgedPrognosisGraves Diseasemedicine.anatomical_structureFemaleAntibodyGoiter NodularImmunoglobulins Thyroid-StimulatingAdultendocrine systemmedicine.medical_specialtyAdolescent030209 endocrinology & metabolismHashimoto DiseaseAntibodiesThyrotropin receptorYoung Adult03 medical and health sciencesInternal medicinemedicineHumansThyroid NeoplasmsAgedbusiness.industryBiochemistry (medical)medicine.diseaseeye diseasesEndocrinologyImmunoassaybiology.proteinbusinessBiomarkers

description

AbstractA rapid and fully automated chemiluminescent immunoassay for the detection of thyrotropin receptor autoantibodies (TSHR-Ab) based on a bridge technology was compared with two bioassays that measure either stimulating (TSAb) or blocking (TBAb) antibodies for the detection and differentiation of TSHR-Ab. A total of 229 patients with various thyroid disorders [151 with Graves’ disease (GD), 35 with Hashimoto’s thyroiditis (HT), 32 with nodular goiter, and 11 with thyroid cancer] were included. The bridge immunoassay was performed according to the manufacturer’s instructions (cut-off>0.55 IU/l). TSAb and TBAb were measured with reporter bioassays. Blocking activity was defined as percent inhibition of luciferase expression relative to induction with bovine TSH alone (cut-off>34% inhibition). TSAb was reported as percentage of specimen-to-reference ratio (> 140 SRR%). The 3 TSHR-Ab assays were negative in all patients with benign euthyroid nodular goiter and differentiated thyroid cancer. In contrast, in all patients with GD, irrespective of the disease duration, TSHR-Ab positivity was present in 127 of 151 (84%) and 140 (93%) for the bridge assay and TSAb bioassay, respectively (p<0.001). Fifteen of 151 (10%) GD samples were positive in the TSAb bioassay but negative in the bridge assay. The bridge assay and the TSAb bioassay correlated positively (r=0.39, p<0.0001) in patients with GD. Both assays detected TSHR-Ab in all ten untreated hyperthyroid patients with GD. In GD patients with a duration of less than six months, 27/29 (93%) and 28 (97%) were TSHR-Ab positive with the bridge and TSAb bioassay, respectively. In comparison, TSHR-Ab were present in two of 35 (6%) and five (14%) HT patients with the bridge and TSAb bio-assay, respectively. TSHR blocking antibodies were present in one (3%) patient with HT and in two (1%) patients with GD; these two GD patients were also bridge assay positive but TSAb bioassay negative. In conclusion, the bridge immunoassay and both bioassays are highly sensitive for the detection of TSHR-Ab. The bridge assay is, however, also positive in the presence of TSHR blocking antibodies detected in a TBAb bioassay.

https://doi.org/10.1055/a-0914-0535