Suppr超能文献

基于微阵列的甲状腺自身抗体亲和力检测

Microarray-Based Avidity Assay for Assessment of Thyroid Autoantibodies.

作者信息

Savvateeva Elena, Sokolova Vera, Yukina Marina, Nuralieva Nurana, Kulagina Elena, Donnikov Maxim, Kovalenko Lyudmila, Kazakova Maria, Troshina Ekaterina, Gryadunov Dmitry

机构信息

Center for Precision Genome Editing and Genetic Technologies for Biomedicine, Engelhardt Institute of Molecular Biology (EIMB), Russian Academy of Sciences, 119991 Moscow, Russia.

Endocrinology Research Centre, Ministry of Health of Russia, 117292 Moscow, Russia.

出版信息

Diagnostics (Basel). 2025 Jan 31;15(3):341. doi: 10.3390/diagnostics15030341.

Abstract

The aim of this study was to evaluate the avidity of thyroid autoantibodies (Abs) in sera of patients with autoimmune thyroid disease (AITD) and thyroid autoantibody carriers without diagnosed AITD. A hydrogel microarray-based multiplex assay with the chaotrope destruction stage was developed to measure the avidity of thyroid disease-associated autoantibodies, including those targeting thyroperoxidase (TPO), thyroglobulin (Tg), and other minor antigens. Evaluation of the assay in three independent cohorts of patients, totaling 266 individuals with and without AITD, demonstrated the heterogeneous avidity of autoantibodies to thyroid proteins. For the confirmation study, the median avidity index (AI) for AbTg was 29.9% in healthy autoantibody carriers, 52.6% for AITD patients, and 92.7% for type 1 diabetes (T1D) thyroid autoantibody carriers. The median AI for AbTPO was 39.9% in healthy carriers, 73.4% in AITD patients, 83.2% in T1D thyroid autoantibody carriers, and 98.5% in AITD patients with thyroid neoplasm. In patients with Hashimoto's thyroiditis and known disease duration, changes in the avidity maturation of AbTPO over time were demonstrated. Longitudinal studies of TPO- and/or Tg-positive healthy individuals (with an interval of 1-2 years between visits) are needed to evaluate the maturation of autoantibody avidity during the asymptomatic phase and to assess the potential of autoantibody avidity as a prognostic marker for disease development.

摘要

本研究的目的是评估自身免疫性甲状腺疾病(AITD)患者以及未确诊AITD的甲状腺自身抗体携带者血清中甲状腺自身抗体(Abs)的亲和力。开发了一种基于水凝胶微阵列的多重检测方法,该方法具有离液剂破坏阶段,用于测量与甲状腺疾病相关的自身抗体的亲和力,包括那些针对甲状腺过氧化物酶(TPO)、甲状腺球蛋白(Tg)和其他次要抗原的自身抗体。在三个独立的患者队列(共266名有或无AITD的个体)中对该检测方法进行评估,结果显示自身抗体对甲状腺蛋白的亲和力存在异质性。在确证研究中,健康自身抗体携带者中抗Tg的中位亲和力指数(AI)为29.9%,AITD患者为52.6%,1型糖尿病(T1D)甲状腺自身抗体携带者为92.7%。健康携带者中抗TPO的中位AI为39.9%,AITD患者为73.4%,T1D甲状腺自身抗体携带者为83.2%,患有甲状腺肿瘤的AITD患者为98.5%。在已知病程的桥本甲状腺炎患者中,显示了抗TPO亲和力成熟随时间的变化。需要对TPO和/或Tg阳性的健康个体进行纵向研究(每次就诊间隔1 - 2年),以评估无症状期自身抗体亲和力的成熟情况,并评估自身抗体亲和力作为疾病发展预后标志物的潜力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/43f9/11817500/546c445ddb54/diagnostics-15-00341-g001.jpg

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验