A novel third-generation TSH receptor antibody (TRAb) enzyme-linked immunosorbent assay based on a murine monoclonal TSH receptor-binding antibody

Research output: Contribution to journalResearch articleContributedpeer-review

Contributors

  • Johannes J. Roggenbuck - , Department of Nuclear Medicine (Author)
  • Miklos Veiczi - , Medipan GmbH (Author)
  • Karsten Conrad - , Institute for Immunology (Author)
  • Peter Schierack - , Brandenburg University of Technology (Author)
  • Gerd Wunderlich - , University Vascular Centre (Author)
  • Joerg Kotzerke - , Department of Nuclear Medicine (Author)
  • Dirk Roggenbuck - , Medipan GmbH (Author)
  • Klaus Zöphel - , University Vascular Centre (Author)

Abstract

TSH receptor (TSHR) autoantibody (TRAb) is the serological hallmark of Graves' disease (GD). Third-generation enzyme-linked immunosorbent assays (ELISAs) using monoclonal TRAbs instead of TSH have been found useful for TRAb analysis recently. For the first time, a mouse monoclonal antibody (mAb) against TSHR was analyzed for TRAb detection and compared with human mAb M22 and TSH by the same competitive binding assay technique. A mouse monoclonal antibody (T7) binding to the TSH receptor and inhibiting TSH binding was generated and used for TRAb analysis in a third-generation ELISA. Obtained TRAb levels were compared with a second-generation TRAb assay employing bovine TSH and a third-generation assay with human mAb M22 as TSHR-binding reagents by investigating 89 patients with GD, 56 with Hashimoto's thyroiditis (HT), 73 with non-autoimmune thyroid diseases, 17 with rheumatoid arthritis, and 100 healthy subjects. The T7-based TRAb ELISA did not reveal a significantly different assay performance (area under the curve [AUC]) in contrast to the TSH and M22-based TRAb ELISAs by receiver operating characteristic (ROC) curve analysis (AUC-T7 0.967, AUC-TSH 0.972, AUC-M22 0.958, p > 0.05, respectively). After adjustment of cutoffs by ROC, all three TRAb ELISAs demonstrated sensitivities and specificities above 89.9% and 96.0%, respectively. Both third-generation TRAb ELISAs showed a tendency for a higher prevalence of TRAb positives in HT in contrast to the second-generation ELISA. Mouse mAbs against the TSHR may be used for the reliable detection of TRAb by third-generation TRAb ELISA. The earlier reported higher sensitivity of third-generation TRAb ELISA in GD needs to be considered in the context of a slightly lower specificity regarding HT.

Details

Original languageEnglish
Pages (from-to)768-776
Number of pages9
JournalImmunologic research
Volume66
Issue number6
Publication statusPublished - Dec 2018
Peer-reviewedYes

External IDs

Scopus 85060763101

Keywords

Sustainable Development Goals

Keywords

  • Animals, Antibodies, Monoclonal/immunology, Arthritis, Rheumatoid/immunology, Enzyme-Linked Immunosorbent Assay/methods, Female, Graves Disease/immunology, Hashimoto Disease/immunology, Humans, Immunoassay/methods, Immunoglobulins, Thyroid-Stimulating/immunology, Male, Mice, Middle Aged, ROC Curve, Receptors, Thyrotropin/immunology, Sensitivity and Specificity, Thyroiditis, Autoimmune/immunology

Library keywords