Ando Takao, Latif Rauf, Pritsker Alla, Moran Thomas, Nagayama Yuji, Davies Terry F
Division of Endocrinology, Diabetes, and Bone Diseases, Department of Medicine, Mount Sinai School of Medicine, New York, New York, USA.
J Clin Invest. 2002 Dec;110(11):1667-74. doi: 10.1172/JCI16991.
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.
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。