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A monoclonal thyroid-stimulating antibody.一种单克隆促甲状腺抗体。
J Clin Invest. 2002 Dec;110(11):1667-74. doi: 10.1172/JCI16991.
2
Thyroid-stimulating autoantibodies in Graves disease preferentially recognize the free A subunit, not the thyrotropin holoreceptor.格雷夫斯病中的促甲状腺素自身抗体优先识别游离的A亚基,而非促甲状腺素全受体。
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A human monoclonal autoantibody to the thyrotropin receptor with thyroid-stimulating blocking activity.一种具有促甲状腺素阻断活性的人促甲状腺素受体单克隆自身抗体。
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4
Antibody-induced modulation of TSH receptor post-translational processing.抗体诱导的促甲状腺激素受体翻译后加工的调节。
J Endocrinol. 2007 Oct;195(1):179-86. doi: 10.1677/JOE-07-0058.
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Characteristics of a monoclonal antibody to the thyrotropin receptor that acts as a powerful thyroid-stimulating autoantibody antagonist.一种针对促甲状腺激素受体的单克隆抗体的特性,该抗体可作为一种强效的甲状腺刺激自身抗体拮抗剂。
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Thyroid-stimulating monoclonal antibodies.促甲状腺单克隆抗体
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Effects of TSH receptor mutations on binding and biological activity of monoclonal antibodies and TSH.促甲状腺激素受体突变对单克隆抗体和促甲状腺激素结合及生物活性的影响。
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Does thyrotropin cleave its cognate receptor?促甲状腺激素会裂解其同源受体吗?
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Evidence that TSH Receptor A-Subunit Multimers, Not Monomers, Drive Antibody Affinity Maturation in Graves' Disease.促甲状腺激素受体A亚基多聚体而非单体驱动格雷夫斯病抗体亲和力成熟的证据。
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Brief Report - Monoclonal Antibodies Illustrate the Difficulties in Measuring Blocking TSH Receptor Antibodies.简报 - 单克隆抗体表明测量阻断 TSH 受体抗体存在困难。
Front Endocrinol (Lausanne). 2022 Jul 15;13:943459. doi: 10.3389/fendo.2022.943459. eCollection 2022.
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Mechanisms in Graves Eye Disease: Apoptosis as the End Point of Insulin-Like Growth Factor 1 Receptor Inhibition.格雷夫斯眼病的发病机制:胰岛素样生长因子 1 受体抑制的终点为细胞凋亡。
Thyroid. 2022 Apr;32(4):429-439. doi: 10.1089/thy.2021.0176.
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Graves' disease.格雷夫斯病。
Nat Rev Dis Primers. 2020 Jul 2;6(1):52. doi: 10.1038/s41572-020-0184-y.
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Molecular Insights Into the Relationship Between Autoimmune Thyroid Diseases and Breast Cancer: A Critical Perspective on Autoimmunity and ER Stress.自身免疫性甲状腺疾病与乳腺癌的关系的分子研究:自身免疫与内质网应激的批判性视角。
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A Modifying Autoantigen in Graves' Disease.格雷夫斯病中的修饰自身抗原。
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Antigenic "Hot- Spots" on the TSH Receptor Hinge Region.促甲状腺激素受体铰链区的抗原“热点”。
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Biased signaling by thyroid-stimulating hormone receptor-specific antibodies determines thyrocyte survival in autoimmunity.甲状腺刺激素受体特异性抗体的信号偏向决定了自身免疫中甲状腺细胞的存活。
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TSH Receptor Signaling Abrogation by a Novel Small Molecule.一种新型小分子对促甲状腺激素受体信号传导的阻断作用
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10
Withdrawn: TSH Receptor Cleavage Into Subunits and Shedding of the A-Subunit; A Molecular and Clinical Perspective.撤回:促甲状腺激素受体裂解为亚基及A亚基脱落;分子与临床视角
Endocr Rev. 2016 Feb;2016(1):23-42. doi: 10.1210/er.2015-1098.2016.1.test.

本文引用的文献

1
Ligand-dependent inhibition of oligomerization at the human thyrotropin receptor.人促甲状腺激素受体上配体依赖性的寡聚化抑制作用
J Biol Chem. 2002 Nov 22;277(47):45059-67. doi: 10.1074/jbc.M206693200. Epub 2002 Sep 9.
2
The TSH receptor reveals itself.促甲状腺激素受体显露出来。
J Clin Invest. 2002 Jul;110(2):161-4. doi: 10.1172/JCI16234.
3
Activation of the cAMP pathway by the TSH receptor involves switching of the ectodomain from a tethered inverse agonist to an agonist.促甲状腺激素(TSH)受体激活cAMP信号通路涉及胞外域从一种锚定的反向激动剂转变为激动剂。
Mol Endocrinol. 2002 Apr;16(4):736-46. doi: 10.1210/mend.16.4.0816.
4
Thyroid-stimulating hormone and thyroid-stimulating hormone receptor structure-function relationships.促甲状腺激素与促甲状腺激素受体的结构-功能关系
Physiol Rev. 2002 Apr;82(2):473-502. doi: 10.1152/physrev.00031.2001.
5
A novel murine model of Graves' hyperthyroidism with intramuscular injection of adenovirus expressing the thyrotropin receptor.一种通过肌肉注射表达促甲状腺激素受体的腺病毒构建的格雷夫斯甲亢新型小鼠模型。
J Immunol. 2002 Mar 15;168(6):2789-94. doi: 10.4049/jimmunol.168.6.2789.
6
Oligomerization of the human thyrotropin receptor: fluorescent protein-tagged hTSHR reveals post-translational complexes.人促甲状腺激素受体的寡聚化:荧光蛋白标记的hTSHR揭示翻译后复合物。
J Biol Chem. 2001 Nov 30;276(48):45217-24. doi: 10.1074/jbc.M103727200. Epub 2001 Sep 4.
7
Epitope analysis of the human thyrotropin (TSH) receptor using monoclonal antibodies.利用单克隆抗体对人促甲状腺激素(TSH)受体进行表位分析。
Thyroid. 2000 Dec;10(12):1051-9. doi: 10.1089/thy.2000.10.1051.
8
The hamster as a model of human visceral leishmaniasis: progressive disease and impaired generation of nitric oxide in the face of a prominent Th1-like cytokine response.仓鼠作为人类内脏利什曼病的模型:面对显著的Th1样细胞因子反应时疾病进展及一氧化氮生成受损。
J Immunol. 2001 Feb 1;166(3):1912-20. doi: 10.4049/jimmunol.166.3.1912.
9
Induction of experimental autoimmune Graves' disease in BALB/c mice.在BALB/c小鼠中诱导实验性自身免疫性格雷夫斯病
J Immunol. 1999 Nov 1;163(9):5157-64.
10
Preparation of monoclonal antibodies to murine platelet glycoprotein IIb/IIIa (alphaIIbbeta3) and other proteins from hamster-mouse interspecies hybridomas.制备针对小鼠血小板糖蛋白IIb/IIIa(αIIbβ3)以及来自仓鼠-小鼠种间杂交瘤的其他蛋白质的单克隆抗体。
Biochem Biophys Res Commun. 1999 Aug 19;262(1):167-73. doi: 10.1006/bbrc.1999.1172.

一种单克隆促甲状腺抗体。

A monoclonal thyroid-stimulating antibody.

作者信息

Ando Takao, Latif Rauf, Pritsker Alla, Moran Thomas, Nagayama Yuji, Davies Terry F

机构信息

Division of Endocrinology, Diabetes, and Bone Diseases, Department of Medicine, Mount Sinai School of Medicine, New York, New York, USA.

出版信息

J Clin Invest. 2002 Dec;110(11):1667-74. doi: 10.1172/JCI16991.

DOI:10.1172/JCI16991
PMID:12464672
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC151640/
Abstract

The thyrotropin receptor, also known as the thyroid-stimulating hormone receptor (TSHR), is the primary antigen of Graves disease. Stimulating TSHR antibodies are the cause of thyroid overstimulation and were originally called long-acting thyroid stimulators due to their prolonged action. Here we report the successful cloning and characterization of a monoclonal antibody (MS-1) with TSHR-stimulating activity. The thyroid-stimulating activity of MS-1 was evident at IgG concentrations as low as 20 ng/ml. MS-1 also competed for radiolabeled TSH binding to the native TSHR and was able to compete for TSH-induced stimulation. MS-1 recognized a conformational epitope within the TSHR alpha (or A) subunit but excluding the receptor cleavage region. Using an assay measuring loss of antibody recognition after cleavage we demonstrated that MS-1, in contrast to TSH, was unable to enhance TSHR posttranslational cleavage. Since receptor cleavage is followed by alpha subunit shedding and receptor degradation, the functional half-life of the receptor may be extended. The isolation and characterization of MS-1 provides a novel explanation for the prolonged thyroid stimulation in this disease which may be secondary to the lack of receptor cleavage in addition to the prolonged half-life of IgG itself.

摘要

促甲状腺激素受体,也被称为甲状腺刺激激素受体(TSHR),是格雷夫斯病的主要抗原。刺激性TSHR抗体是甲状腺过度刺激的原因,最初因其作用时间延长而被称为长效甲状腺刺激素。在此,我们报告了一种具有TSHR刺激活性的单克隆抗体(MS-1)的成功克隆和特性鉴定。MS-1在低至20 ng/ml的IgG浓度下就具有明显的甲状腺刺激活性。MS-1还能竞争放射性标记的TSH与天然TSHR的结合,并能够竞争TSH诱导的刺激作用。MS-1识别TSHRα(或A)亚基内的一个构象表位,但不包括受体裂解区域。通过一种测量裂解后抗体识别丧失的测定方法,我们证明与TSH不同,MS-1不能增强TSHR的翻译后裂解。由于受体裂解后会伴随α亚基脱落和受体降解,受体的功能半衰期可能会延长。MS-1的分离和特性鉴定为该疾病中甲状腺刺激时间延长提供了一种新的解释,这可能是除了IgG本身半衰期延长外,还继发于缺乏受体裂解。