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Usage Information

Genetic immunization of outbred mice with thyrotropin receptor cDNA provides a model of Graves’ disease
Sabine Costagliola, Marie-Christine Many, Jean-François Denef, Joachim Pohlenz, Samuel Refetoff, Gilbert Vassart
Sabine Costagliola, Marie-Christine Many, Jean-François Denef, Joachim Pohlenz, Samuel Refetoff, Gilbert Vassart
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Article

Genetic immunization of outbred mice with thyrotropin receptor cDNA provides a model of Graves’ disease

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Abstract

We performed genetic immunization of outbred NMRI mice, using a cDNA encoding the human thyrotropin receptor (TSHr). All mice produced antibodies capable of recognizing the recombinant receptor expressed at the surface of stably transfected Chinese hamster ovary (CHO) cells, and sera from most of the immunized mice blocked TSH-dependent stimulation of cAMP accumulation in cells expressing the TSHr. Five out of 29 female mice showed sign of hyperthyroidism including elevated total T4 and suppressed TSH levels. The serum of these mice contained thyroid-stimulating activity, as measured in a classic assay using CHO cells expressing recombinant TSHr. In contrast, only 1 male out of 30 had moderately elevated serum total T4 with undetectable TSH values. The hyperthyroid animals had goiters with extensive lymphocytic infiltration, characteristic of a Th2 immune response. In addition, these animals displayed ocular signs reminiscent of Graves’ ophthalmopathy, including edema, deposit of amorphous material, and cellular infiltration of their extraocular muscles. Our results demonstrate that genetic immunization of outbred NMRI mice with the human TSHr provides the most convincing murine model of Graves’ disease available to date.

Authors

Sabine Costagliola, Marie-Christine Many, Jean-François Denef, Joachim Pohlenz, Samuel Refetoff, Gilbert Vassart

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Usage data is cumulative from August 2025 through August 2026.

Usage JCI PMC
Text version 679 36
PDF 156 17
Figure 659 11
Table 94 0
Citation downloads 209 0
Totals 1,797 64
Total Views 1,861
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Usage information is collected from two different sources: this site (JCI) and Pubmed Central (PMC). JCI information (compiled daily) shows human readership based on methods we employ to screen out robotic usage. PMC information (aggregated monthly) is also similarly screened of robotic usage.

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ISSN: 0021-9738 (print), 1558-8238 (online)

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