Horm Metab Res 2015; 47(10): 797-803
DOI: 10.1055/s-0035-1555956
Review

Modeling Graves’ Orbitopathy in Experimental Graves’ Disease

J. P. Banga
1   Faculty of Life Sciences & Medicine, King’s College London, The Rayne Institute, London, UK
2   Department of Ophthalmology, University of Duisburg-Essen, Essen, Germany
,
S. Moshkelgosha
1   Faculty of Life Sciences & Medicine, King’s College London, The Rayne Institute, London, UK
2   Department of Ophthalmology, University of Duisburg-Essen, Essen, Germany
,
U. Berchner-Pfannschmidt
2   Department of Ophthalmology, University of Duisburg-Essen, Essen, Germany
,
A. Eckstein
2   Department of Ophthalmology, University of Duisburg-Essen, Essen, Germany
› Author Affiliations
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Abstract

Graves’ orbitopathy (GO), also known as thyroid eye disease is an inflammatory disease of the orbital tissue of the eye that arises as a consequence of autoimmune thyroid disease. The central feature of the disease is the production of antibodies to the thyrotropin hormone receptor (TSHR) that modulate the function of the receptor leading to autoimmune hyperthyroidism and GO. Over the years, all viable preclinical models of Graves’ disease have been incomplete and singularly failed to progress in the treatment of orbital complications. A new mouse model of GO based upon immunogenic presentation of human TSHR A-subunit plasmid by close field electroporation is shown to lead to induction of prolonged functional antibodies to TSHR resulting in chronic disease with subsequent progression to GO. The stable preclinical GO model exhibited pathologies reminiscent of human disease characterized by orbital remodeling by inflammation and adipogenesis. Inflammatory lesions characterized by CD3+ T cells and macrophages were localized in the orbital muscle tissue. This was accompanied by extensive adipogenesis of orbital fat in some immune animals. Surprisingly, other signs of orbital involvement were reminiscent of eyelid inflammation involving chemosis, with dilated and congested orbital blood vessels. More recently, the model is replicated in the author’s independent laboratories. The pre-clinical model will provide the basis to study the pathogenic and regulatory roles of immune T and B cells and their subpopulations to understand the initiation, pathophysiology, and progression of GO.



Publication History

Received: 20 April 2015

Accepted: 08 July 2015

Article published online:
19 August 2015

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