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首页> 外文期刊>Clinical and Experimental Immunology: An Official Journal of the British Society for Immunology >Epitope recognition patterns of thyroglobulin antibody in sera from patients with Hashimoto's thyroiditis on different thyroid functional status
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Epitope recognition patterns of thyroglobulin antibody in sera from patients with Hashimoto's thyroiditis on different thyroid functional status

机译:不同甲状腺功能状态桥本甲状腺炎患者血清甲状腺球蛋白抗体的抗原表位识别模式

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摘要

Thyroglobulin antibody (TgAb) is a diagnostic serological marker of Hashimoto's thyroiditis (HT). The pathogenesis of HT progression from euthyroidism to hypothyroidism is still not clear. Epitope recognition patterns of TgAb have been shown to be different in individuals who are euthyroid or who have clinical disease. The aim of our study was to investigate the role of thyroglobulin (Tg) epitope specificities in HT progression. Sera from 107 patients with newly diagnosed HT were collected and divided into three groups: patients with hypothyroidism (H, n=39), subclinical hypothyroidism (sH, n=31) and euthyroidism (Eu, n=37). A panel of Tg murine monoclonal antibodies (mAb: PB2, 5E6, 1D4, 5F9, Tg6) and a hircine pAb (N15) were employed as the probe antibodies to define the antigenic determinants recognized by HT sera on competitive enzyme-linked immunosorbent assays (ELISAs). Eight of 39 sera samples in H and seven of 31 in sH inhibited PB2 binding, respectively, whereas none did in Eu. The ratio of sera samples, inhibiting PB2 binding in Eu, was significantly lower than that in H (P=0·011) and in sH (P=0·008). For N15, five of 39 sera samples in H, six of 31 in sH and 15 of 37 in Eu inhibited its binding, respectively. The ratio of sera samples, inhibiting N15 binding in Eu, was significantly higher than that in H (P=0·013). Our study demonstrated that HT patients in different thyroid functional status exhibited different Tg epitope recognition patterns. Epitope patterns of TgAb might be used as a prediction marker of HT progression.
机译:甲状腺球蛋白抗体(TgAb)是桥本甲状腺炎(HT)的诊断血清学标志。从正常甲状腺功能减退到甲状腺功能减退的HT发病机制仍不清楚。在甲状腺功能正常或患有临床疾病的个体中,TgAb的表位识别模式已显示出不同。我们研究的目的是研究甲状腺球蛋白(Tg)表位特异性在HT进展中的作用。收集107例新诊断为HT的患者的血清,将其分为三组:甲状腺功能减退症(H,n = 39),亚临床甲状腺功能减退症(sH,n = 31)和甲状腺功能正常(Eu,n = 37)。使用一组Tg鼠单克隆抗体(mAb:PB2、5E6、1D4、5F9,Tg6)和水痘pAb(N15)作为探针抗体,以确定在竞争性酶联免疫吸附测定中HT血清识别的抗原决定簇( ELISA)。 H中39个血清样品中的八个和sH中31个血清样品中的七个分别抑制PB2结合,而Eu中没有一个。抑制Eu中PB2结合的血清样品的比例显着低于H(P = 0·011)和sH(P = 0·008)。对于N15,H中39个血清样品中的五个,sH中31个血清中的六个和Eu中37个中的15个分别抑制了其结合。抑制Eu中N15结合的血清样品比例显着高于H(P = 0·013)。我们的研究表明,处于不同甲状腺功能状态的HT患者表现出不同的Tg表位识别模式。 TgAb的表位模式可以用作HT进展的预测标志。

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