Literature DB >> 28099999

High-level intrathymic thyrotrophin receptor expression in thyroiditis-prone mice protects against the spontaneous generation of pathogenic thyrotrophin receptor autoantibodies.

S M McLachlan1, H A Aliesky1, B Banuelos1, S Lesage2, R Collin2, B Rapoport1.   

Abstract

The thyrotrophin receptor (TSHR) A-subunit is the autoantigen targeted by pathogenic autoantibodies that cause Graves' hyperthyroidism, a common autoimmune disease in humans. Previously, we reported that pathogenic TSHR antibodies develop spontaneously in thyroiditis-susceptible non-obese diabetic (NOD).H2h4 mice bearing a human TSHR A-subunit transgene, which is expressed at low levels in both the thyroid and thymus (Lo-expressor transgene). The present study tested recent evidence that high intrathymic TSHR expression protects against the development of pathogenic TSHR antibodies in humans. By successive back-crossing, we transferred to the NOD.H2h4 background a human TSHR A-subunit transgene expressed at high levels in the thyroid and thymus (Hi-expressor transgene). In the sixth back-cross generation (> 98% NOD.H2h4 genome), only transgenic offspring produced spontaneously immunoglobulin (Ig)G class non-pathogenic human TSHR A-subunit antibodies. In contrast, both transgenic and non-transgenic offspring developed antibodies to thyroglobulin and thyroid peroxidase. However, non-pathogenic human TSHR antibody levels in Hi-expressor offspring were lower than in Lo-expressor transgenic mice. Moreover, pathogenic TSHR antibodies, detected by inhibition of TSH binding to the TSHR, only developed in back-cross offspring bearing the Lo-expressor, but not the Hi-expressor, transgene. High versus low expression human TSHR A-subunit in the NOD.H2h4 thymus was not explained by the transgene locations, namely chromosome 2 (127-147 Mb; Hi-expressor) and chromosome 1 (22.9-39.3 Mb; low expressor). Nevertheless, using thyroiditis-prone NOD.H2h4 mice and two transgenic lines, our data support the association from human studies that low intrathymic TSHR expression is associated with susceptibility to developing pathogenic TSHR antibodies, while high intrathymic TSHR expression is protective.
© 2017 British Society for Immunology.

Entities:  

Keywords:  Graves' disease; TSHR autoantibodies; autoimmunity; intrathymic transcription; thyroid autoantigens; tolerance

Mesh:

Substances:

Year:  2017        PMID: 28099999      PMCID: PMC5383439          DOI: 10.1111/cei.12928

Source DB:  PubMed          Journal:  Clin Exp Immunol        ISSN: 0009-9104            Impact factor:   4.330


  45 in total

1.  Spontaneous autoimmune thyroiditis in NOD.H-2h4 mice.

Authors:  H Braley-Mullen; G C Sharp; B Medling; H Tang
Journal:  J Autoimmun       Date:  1999-05       Impact factor: 7.094

2.  Iodine-induced autoimmune thyroiditis in NOD-H-2h4 mice.

Authors:  L Rasooly; C L Burek; N R Rose
Journal:  Clin Immunol Immunopathol       Date:  1996-12

3.  Studies in mice deficient for the autoimmune regulator (Aire) and transgenic for the thyrotropin receptor reveal a role for Aire in tolerance for thyroid autoantigens.

Authors:  Alexander V Misharin; Yuji Nagayama; Holly A Aliesky; Basil Rapoport; Sandra M McLachlan
Journal:  Endocrinology       Date:  2009-03-05       Impact factor: 4.736

4.  Targeted expression of the human thyrotropin receptor A-subunit to the mouse thyroid: insight into overcoming the lack of response to A-subunit adenovirus immunization.

Authors:  Pavel N Pichurin; Chun-Rong Chen; Gregorio D Chazenbalk; Holly Aliesky; Nancy Pham; Basil Rapoport; Sandra M McLachlan
Journal:  J Immunol       Date:  2006-01-01       Impact factor: 5.422

5.  Both CD4(+) T cells and CD8(+) T cells are required for iodine accelerated thyroiditis in NOD mice.

Authors:  P R Hutchings; S Verma; J M Phillips; S Z Harach; S Howlett; A Cooke
Journal:  Cell Immunol       Date:  1999-03-15       Impact factor: 4.868

6.  Relationship between immunological structure and biochemical properties of human thyroid peroxidase.

Authors:  J Ruf; M E Toubert; B Czarnocka; J M Durand-Gorde; M Ferrand; P Carayon
Journal:  Endocrinology       Date:  1989-09       Impact factor: 4.736

7.  Requirement for Transcription Factor Ets1 in B Cell Tolerance to Self-Antigens.

Authors:  Lisa Russell; Shinu John; Jaime Cullen; Wei Luo; Mark J Shlomchik; Lee Ann Garrett-Sinha
Journal:  J Immunol       Date:  2015-09-09       Impact factor: 5.422

Review 8.  Mechanisms of autoimmune thyroid diseases: from genetics to epigenetics.

Authors:  Yaron Tomer
Journal:  Annu Rev Pathol       Date:  2014       Impact factor: 23.472

9.  The thyrotropin receptor autoantigen in Graves disease is the culprit as well as the victim.

Authors:  Chun-Rong Chen; Pavel Pichurin; Yuji Nagayama; Francesco Latrofa; Basil Rapoport; Sandra M McLachlan
Journal:  J Clin Invest       Date:  2003-06       Impact factor: 14.808

10.  Thymic negative selection is functional in NOD mice.

Authors:  Michael Mingueneau; Wenyu Jiang; Markus Feuerer; Diane Mathis; Christophe Benoist
Journal:  J Exp Med       Date:  2012-02-13       Impact factor: 14.307

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  12 in total

1.  Nanoparticles Bearing TSH Receptor Protein and a Tolerogenic Molecule Do Not Induce Immune Tolerance but Exacerbate Thyroid Autoimmunity in hTSHR/NOD.H2h4 Mice.

Authors:  Sandra M McLachlan; Holly A Aliesky; Basil Rapoport
Journal:  J Immunol       Date:  2019-04-03       Impact factor: 5.422

2.  A Mouse Thyrotropin Receptor A-Subunit Transgene Expressed in Thyroiditis-Prone Mice May Provide Insight into Why Graves' Disease Only Occurs in Humans.

Authors:  Sandra M McLachlan; Holly A Aliesky; Basil Rapoport
Journal:  Thyroid       Date:  2019-07-03       Impact factor: 6.568

3.  Genes Outside the Major Histocompatibility Complex Locus Are Linked to the Development of Thyroid Autoantibodies and Thyroiditis in NOD.H2h4 Mice.

Authors:  Sandra M McLachlan; Sylvie Lesage; Roxanne Collin; Bianca Banuelos; Holly A Aliesky; Basil Rapoport
Journal:  Endocrinology       Date:  2017-04-01       Impact factor: 4.736

4.  A Modifying Autoantigen in Graves' Disease.

Authors:  Rauf Latif; Mihaly Mezei; Syed A Morshed; Risheng Ma; Rachel Ehrlich; Terry F Davies
Journal:  Endocrinology       Date:  2019-05-01       Impact factor: 4.736

5.  Variable Effects of Dietary Selenium in Mice That Spontaneously Develop a Spectrum of Thyroid Autoantibodies.

Authors:  Sandra M McLachlan; Holly Aliesky; Bianca Banuelos; Shane S Que Hee; Basil Rapoport
Journal:  Endocrinology       Date:  2017-11-01       Impact factor: 4.736

Review 6.  A transgenic mouse that spontaneously develops pathogenic TSH receptor antibodies will facilitate study of antigen-specific immunotherapy for human Graves' disease.

Authors:  Sandra M McLachlan; Basil Rapoport
Journal:  Endocrine       Date:  2019-09-27       Impact factor: 3.633

7.  Genetic immunization with mouse thyrotrophin hormone receptor plasmid breaks self-tolerance for a murine model of autoimmune thyroid disease and Graves' orbitopathy.

Authors:  A Schlüter; M Horstmann; S Diaz-Cano; S Plöhn; K Stähr; S Mattheis; M Oeverhaus; S Lang; U Flögel; U Berchner-Pfannschmidt; A Eckstein; J P Banga
Journal:  Clin Exp Immunol       Date:  2017-11-17       Impact factor: 4.330

Review 8.  Thyroid Autoantibodies Display both "Original Antigenic Sin" and Epitope Spreading.

Authors:  Sandra M McLachlan; Basil Rapoport
Journal:  Front Immunol       Date:  2017-12-20       Impact factor: 7.561

9.  Regulation of TSHR Expression in the Thyroid and Thymus May Contribute to TSHR Tolerance Failure in Graves' Disease Patients via Two Distinct Mechanisms.

Authors:  Ana Marín-Sánchez; Daniel Álvarez-Sierra; Oscar González; Ana Lucas-Martin; Alicia Sellés-Sánchez; Francesc Rudilla; Emma Enrich; Roger Colobran; Ricardo Pujol-Borrell
Journal:  Front Immunol       Date:  2019-07-18       Impact factor: 7.561

10.  Thyroid Hemiagenesis in a Thyroiditis Prone Mouse Strain.

Authors:  Sandra M McLachlan; Holly A Aliesky; Priscilla Garcia; Bianca Banuelos; Basil Rapoport
Journal:  Eur Thyroid J       Date:  2018-07-18
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