Graves病、桥本甲状腺炎和重叠综合征患者甲状腺过氧化物酶抗体的表位特异性

IF 4.2 Q1 ENDOCRINOLOGY & METABOLISM
Maira Espenbetova , Nina Kuzmina , Alexandr Zubkov , Venera Akhmetova , Zhanar Zamanbekova , Ainur Krykpaeva , Zhanar Zhumanbayeva , Kuralay Amrenova , Zhanargul Smailova , Natalya Glushkova
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引用次数: 2

摘要

抗甲状腺过氧化物酶抗体(anti-TPO)是甲状腺自身免疫性疾病(TAIDs)的临床标志物。通过试图阐明不同TAIDs患者自身抗体水平异质性的原因,阐明GD和HT的病理生理学成为可能。目的探讨桥本甲状腺炎(HT)、Graves病(GD)和重叠综合征患者抗tpo识别表位的异质性。方法对398例GD、HT和重叠综合征患者进行横断面研究,分析TPO与单克隆抗体(mab)的表位特异性和结合常数。使用了10个针对TPO的单抗,其中5个与天然TPO反应,其余与变性TPO反应。结果HT患者血清自身抗体对MAb63结合的抑制作用明显高于GD患者,分别为59.62%和54.02% (p = 0.001)。GD患者血清中抗tpos对MAb77结合的抑制作用明显高于HT患者,分别为54.36%和51.13% (p = 0.047)。抗tpo浓度大于1000 IU/ml的患者血清中MAb45的结合更受抑制(58.36%)。重叠综合征患者血清对MAb63结合的抑制作用低于无重叠综合征患者,分别为52.47%和58.81% (p = 0.043)。结论利用单克隆抗体定位TPO抗原表位可以提高不同甲状腺自身免疫的鉴别诊断。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Epitopes specificity of antibodies to thyroid peroxidase in patients with Graves’ disease, Hashimoto’s thyroiditis and overlap-syndrome

Background

Antibodies against thyroid peroxidase (anti-TPO) serve as clinical markers of thyroid autoimmune diseases (TAIDs). By trying to elucidate the causes of heterogeneity in autoantibody levels among patients with different TAIDs it becomes possible to clarify the pathophysiology of GD and HT.

Objective

To investigate the heterogeneity of epitopes recognized by anti-TPO in patients with Hashimoto’s thyroiditis (HT), Graves’ disease (GD) and overlap-syndrome.

Methods

We carried out a cross-sectional study on 398 patients with GD, HT and overlap syndrome and analyzed the specificity of epitopes and binding constants of TPO with monoclonal antibodies (MAbs). Ten MAbs to TPO were used, of which five were reactive with native TPO and the rest were reactive with denaturated TPO.

Results

The autoantibodies in blood serum of HT patients inhibited the binding of MAb63 more significantly than those in serum of GD patients: 59.62 % versus 54.02 %, respectively (p = 0.001). The anti-TPOs in serum of GD patients inhibited the binding of MAb77 more significantly than those in serum of HT patients: 54.36 % versus 51.13 %, respectively (p = 0.047). The binding of MAb45 was more inhibited in serum of patients with anti-TPO concentration over 1000 IU/ml (58.36 %). The blood serum of patients with overlap-syndrome showed less significant inhibition of MAb63 binding than that of patients with no overlap-syndrome: 52.47 % versus 58.81 %, respectively (p = 0.043).

Conclusion

Mapping the epitopes to TPO with the help of MAbs may improve the differential diagnosis between different thyroid autoimmunities.

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来源期刊
CiteScore
6.10
自引率
0.00%
发文量
24
审稿时长
16 weeks
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