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在存在甲状腺球蛋白抗体的情况下测定血清甲状腺球蛋白。

The measurement of serum thyroglobulin in the presence of thyroglobulin antibodies.

作者信息

Ratcliffe J G, Ayoub L A, Pearson D

出版信息

Clin Endocrinol (Oxf). 1981 Nov;15(5):507-18. doi: 10.1111/j.1365-2265.1981.tb00695.x.

Abstract

In a significant proportion of patients with thyroid disorders, thyroglobulin antibodies (TgAb) invalidate double-antibody radioimmunoassays (RIA) for thyroglobulin (Tg). A modified RIA procedure for determining serum Tg in the presence of TgAb, is described. Two measurements are made on each sample. a Ratio of immunoglobulin (Ig)-bound thyroglobulin to free thyroglobulin (bound:free ratio). This is measured by the distribution of a trace quantity of 125I-Tg between bound and free fractions. b Concentration of free, i.e. unbound thyroglobulin. This is measured in the supernatant after precipitation of IgG-bound Tg. Then, bound Tg=B:F x (free Tg) and total Tg=(bound Tg)+(free Tg). Critical factors examined in the validation of the modified method were: (1) use of immunologically intact 125I-Tg (specific activity less than or equal to 5 mCi/mg); (2) equilibration of tracer Tg with endogenous serum Tg, and (3) clean separation of IgG-bound and free fractions of Tg with goat anti-human IgG. Recovery of added Tg in the presence of TgAb was 105% and interassay precision of total Tg assay was less than or equal to 9.3%. In euthyroid subjects without TgAb, the correlation between total Tg levels by the modified and standard double-antibody method was 0.931. The correlation was much poorer in the presence of TgAb (r=0.752) reflecting their interference in the standard method. Reference ranges for serum total Tg levels by the modified method in euthyroid, hyper- and hypothyroid subjects with and without TgAb are detailed.

摘要

在相当一部分甲状腺疾病患者中,甲状腺球蛋白抗体(TgAb)会使甲状腺球蛋白(Tg)的双抗体放射免疫分析(RIA)结果无效。本文描述了一种在存在TgAb的情况下测定血清Tg的改良RIA方法。对每个样本进行两次测量。a免疫球蛋白(Ig)结合的甲状腺球蛋白与游离甲状腺球蛋白的比值(结合:游离比值)。通过微量125I-Tg在结合和游离部分之间的分布来测量。b游离即未结合甲状腺球蛋白的浓度。在沉淀IgG结合的Tg后的上清液中进行测量。然后,结合Tg = B:F×(游离Tg),总Tg =(结合Tg)+(游离Tg)。在改良方法验证中检查的关键因素包括:(1)使用免疫活性完整的125I-Tg(比活度小于或等于5 mCi/mg);(2)示踪剂Tg与内源性血清Tg的平衡,以及(3)用山羊抗人IgG将Tg的IgG结合部分和游离部分干净分离。在存在TgAb的情况下添加Tg的回收率为105%,总Tg测定的批间精密度小于或等于9.3%。在无TgAb的甲状腺功能正常受试者中,改良法与标准双抗体法测定的总Tg水平之间的相关性为0.931。在存在TgAb的情况下相关性差得多(r = 0.752),这反映了它们对标准方法的干扰。详细列出了改良法在有和无TgAb的甲状腺功能正常、甲状腺功能亢进和甲状腺功能减退受试者中血清总Tg水平的参考范围。

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