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使用环磷酸腺苷门控钙通道和水母发光蛋白检测促甲状腺素抗体的快速生物测定法。

Rapid bioassay for detection of thyroid-stimulating antibodies using cyclic adenosine monophosphate-gated calcium channel and aequorin.

作者信息

Araki Naohiro, Iida Mitsuru, Amino Nobuyuki, Morita Shinji, Ide Akane, Nishihara Eijun, Ito Mitsuru, Saito Jun, Nishikawa Tetsuo, Katsuragi Kiyonori, Miyauchi Akira

机构信息

Diagnostic Division, Otsuka Pharmaceutical Co. Ltd., Tokushima, Japan.

Department of Internal Medicine, Kuma Hospital, Kobe, Japan.

出版信息

Eur Thyroid J. 2015 Mar;4(1):14-9. doi: 10.1159/000371740. Epub 2015 Feb 19.

Abstract

BACKGROUND

Thyroid-stimulating antibodies (TSAb) are known to be responsible for hyperthyroidism in Graves' disease (GD). The conventional methods to measure TSAb depend on cell-based assays that require cumbersome procedures and a sterilized tissue culture technique. The aim of the present study was to develop a ready-to-use cell-based assay for measuring TSAb activity without requiring sterilized conditions.

METHODS

We developed a new assay kit using a frozen Chinese hamster ovary cell line expressing the thyroid-stimulating hormone receptor, cyclic adenosine monophosphate (cAMP)-gated calcium channel and aequorin, tentatively named the aequorin TSAb assay. Activated stimulatory G-protein-coupled adenylate cyclase increases intracellular cAMP, which then binds to the cyclic nucleotide-gated calcium channel. Activation of this channel allows Ca(2+) to enter the cell, and the influx of Ca(2+) can be measured with aequorin, which is quantified by a luminometer. Results can be obtained in only 4 h without sterilized conditions. TSAb activities were expressed by international units using the NIBSC 08/204 standard.

RESULTS

Positive results of aequorin TSAb were obtained in 197 of 199 (98.9%) of untreated patients with GD. Only 1 of 42 (2.3%) patients with painless thyroiditis had a weakly positive aequorin TSAb. All 45 patients with subacute thyroiditis and 185 normal subjects showed negative aequorin TSAb. As for chronic thyroiditis, all 52 euthyroid patients showed negative aequorin TSAb, but 8 of 50 (16.0%) hypothyroid patients had a positive reaction. However, these positive reactions were not induced by serum thyroid-stimulating hormone (TSH) and were thought to be induced by the stimulating activity of anti-TSH receptor immunoglobulins. Conventional porcine TSAb and Elecsys thyroid-stimulating hormone receptor antibodies were positive in 69.3 and 95.5% of GD, respectively.

CONCLUSION

The aequorin TSAb assay was positive in 98.9% of GD and was more sensitive than the conventional assay. This assay can be conducted in only 4 h without sterilized conditions and is practically useful in general clinical laboratories.

摘要

背景

已知促甲状腺素抗体(TSAb)是格雷夫斯病(GD)中导致甲状腺功能亢进的原因。测量TSAb的传统方法依赖于基于细胞的检测,这种检测需要繁琐的程序和无菌的组织培养技术。本研究的目的是开发一种无需无菌条件即可用于测量TSAb活性的即用型基于细胞的检测方法。

方法

我们开发了一种新的检测试剂盒,使用表达促甲状腺激素受体、环磷酸腺苷(cAMP)门控钙通道和水母发光蛋白的冷冻中国仓鼠卵巢细胞系,暂定名为水母发光蛋白TSAb检测法。激活的刺激性G蛋白偶联腺苷酸环化酶会增加细胞内cAMP,然后cAMP与环核苷酸门控钙通道结合。该通道的激活使Ca(2+)进入细胞,Ca(2+)的流入可以用水母发光蛋白测量,水母发光蛋白通过发光计进行定量。无需无菌条件,仅4小时即可获得结果。TSAb活性以国际单位表示,采用NIBSC 08/204标准。

结果

199例未经治疗的GD患者中有197例(98.9%)水母发光蛋白TSAb检测结果为阳性。42例无痛性甲状腺炎患者中只有1例(2.3%)水母发光蛋白TSAb弱阳性。45例亚急性甲状腺炎患者和185例正常受试者的水母发光蛋白TSAb均为阴性。对于慢性甲状腺炎,52例甲状腺功能正常的患者水母发光蛋白TSAb均为阴性,但50例甲状腺功能减退患者中有8例(16.0%)呈阳性反应。然而,这些阳性反应不是由血清促甲状腺激素(TSH)诱导的,被认为是由抗TSH受体免疫球蛋白的刺激活性诱导的。传统的猪TSAb和电化学发光法促甲状腺激素受体抗体在GD中的阳性率分别为69.3%和95.5%。

结论

水母发光蛋白TSAb检测法在98.9%的GD患者中呈阳性,比传统检测更敏感。该检测无需无菌条件,仅4小时即可完成,在一般临床实验室中具有实际应用价值。

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