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Thyrotropin receptor antibodies and Graves’ orbitopathy

CONTEXT AND PURPOSE: The thyrotropin receptor (TSHR) is the key autoantigen in Graves’ disease (GD) and associated orbitopathy (GO). Antibodies targeting the TSHR (TSHR-Ab) impact the pathogenesis and the course of GO. This review discusses the role and clinical relevance of TSHR-Ab in GO. METHODS:...

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Autores principales: Diana, T., Ponto, K. A., Kahaly, G. J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer International Publishing 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8310479/
https://www.ncbi.nlm.nih.gov/pubmed/32749654
http://dx.doi.org/10.1007/s40618-020-01380-9
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author Diana, T.
Ponto, K. A.
Kahaly, G. J.
author_facet Diana, T.
Ponto, K. A.
Kahaly, G. J.
author_sort Diana, T.
collection PubMed
description CONTEXT AND PURPOSE: The thyrotropin receptor (TSHR) is the key autoantigen in Graves’ disease (GD) and associated orbitopathy (GO). Antibodies targeting the TSHR (TSHR-Ab) impact the pathogenesis and the course of GO. This review discusses the role and clinical relevance of TSHR-Ab in GO. METHODS: Review of the current and pertinent literature. RESULTS: GO is the most common extrathyroidal manifestation of GD and is caused by persistent, unregulated stimulation of TSHR-expressing orbital target cells (e.g. fibroblasts and pre-adipocytes). Serum TSHR-Ab and more specifically, the stimulatory Ab (TSAb) are observed in the vast majority of patients with GD and GO. TSHR-Ab are a sensitive serological parameter for the differential diagnosis of GO. TSHR-Ab can be detected either with conventional binding immunoassays that measure binding of Ab to the TSHR or with cell-based bioassays that provide information on their functional activity and potency. Knowledge of the biological activity and not simply the presence or absence of TSHR-Ab has relevant clinical implications e.g. predicting de-novo development or exacerbation of pre-existing GO. TSAb are specific biomarkers of GD/GO and responsible for many of its clinical manifestations. TSAb strongly correlate with the clinical activity and clinical severity of GO. Further, the magnitude of TSAb indicates the onset and acuity of sight-threatening GO (optic neuropathy). Baseline serum values of TSAb and especially dilution analysis of TSAb significantly differentiate between thyroidal GD only versus GD + GO. CONCLUSION: Measurement of functional TSHR-Ab, especially TSAb, is clinically relevant for the differential diagnosis and management of GO.
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spelling pubmed-83104792021-08-12 Thyrotropin receptor antibodies and Graves’ orbitopathy Diana, T. Ponto, K. A. Kahaly, G. J. J Endocrinol Invest Short Review CONTEXT AND PURPOSE: The thyrotropin receptor (TSHR) is the key autoantigen in Graves’ disease (GD) and associated orbitopathy (GO). Antibodies targeting the TSHR (TSHR-Ab) impact the pathogenesis and the course of GO. This review discusses the role and clinical relevance of TSHR-Ab in GO. METHODS: Review of the current and pertinent literature. RESULTS: GO is the most common extrathyroidal manifestation of GD and is caused by persistent, unregulated stimulation of TSHR-expressing orbital target cells (e.g. fibroblasts and pre-adipocytes). Serum TSHR-Ab and more specifically, the stimulatory Ab (TSAb) are observed in the vast majority of patients with GD and GO. TSHR-Ab are a sensitive serological parameter for the differential diagnosis of GO. TSHR-Ab can be detected either with conventional binding immunoassays that measure binding of Ab to the TSHR or with cell-based bioassays that provide information on their functional activity and potency. Knowledge of the biological activity and not simply the presence or absence of TSHR-Ab has relevant clinical implications e.g. predicting de-novo development or exacerbation of pre-existing GO. TSAb are specific biomarkers of GD/GO and responsible for many of its clinical manifestations. TSAb strongly correlate with the clinical activity and clinical severity of GO. Further, the magnitude of TSAb indicates the onset and acuity of sight-threatening GO (optic neuropathy). Baseline serum values of TSAb and especially dilution analysis of TSAb significantly differentiate between thyroidal GD only versus GD + GO. CONCLUSION: Measurement of functional TSHR-Ab, especially TSAb, is clinically relevant for the differential diagnosis and management of GO. Springer International Publishing 2020-08-04 2021 /pmc/articles/PMC8310479/ /pubmed/32749654 http://dx.doi.org/10.1007/s40618-020-01380-9 Text en © The Author(s) 2020, corrected publication 2021 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Short Review
Diana, T.
Ponto, K. A.
Kahaly, G. J.
Thyrotropin receptor antibodies and Graves’ orbitopathy
title Thyrotropin receptor antibodies and Graves’ orbitopathy
title_full Thyrotropin receptor antibodies and Graves’ orbitopathy
title_fullStr Thyrotropin receptor antibodies and Graves’ orbitopathy
title_full_unstemmed Thyrotropin receptor antibodies and Graves’ orbitopathy
title_short Thyrotropin receptor antibodies and Graves’ orbitopathy
title_sort thyrotropin receptor antibodies and graves’ orbitopathy
topic Short Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8310479/
https://www.ncbi.nlm.nih.gov/pubmed/32749654
http://dx.doi.org/10.1007/s40618-020-01380-9
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