Hovens G C J, Buiting A M J, Karperien M, Ballieux B E P B, van der Pluijm G, Pereira A M, Romijn J A, Smit J W A
Department of Endocrinology, Leiden University Medical Center, Leiden, Netherlands.
Clin Endocrinol (Oxf). 2006 Apr;64(4):429-35. doi: 10.1111/j.1365-2265.2006.02487.x.
TSH receptor antibodies (TBII) in Graves' disease (GD) may be TSH receptor stimulating (TSAb) and blocking (TBAb) antibodies. In commercially available assays however, only total TBII titres can be measured, without discriminating between TSAb and TBAb.
To design a TBII bioassay to detect of TSAb and to correlate TSAb activity with severity of hyperthyroidism in de novo GD patients.
Thirty-five patients with de novo GD and 27 controls.
The JP-26-26 cell line, which constitutively expresses the TSH receptor (TSHR), was stably transfected with a cyclic adenosine monophosphate responsive element--luciferase construct. The clone B1 exhibited a near linear increase in luminescence from 0.2 mU/l to 50 mU/l bovine TSH and was used as a TBII bioassay. TBII, free T4 and TSH were measured in the sera of all patients and controls.
In the sera of 35 GD patients, TBII titres did not correlate with serum free T4 concentrations. In contrast, a strong and highly significant correlation was found between TSHR stimulating activity (luminescence) as measured with the TBII bioassay and serum free T4 levels (R = 0.80, P < 0.001). Interestingly, the luminescence/TBII ratio had a wide range at low TBII titres, whereas high TBII titres were associated with a low degree of TSHR activation. The TBII bioassay also detected TBAb in GD patients who spontaneously developed hypothyroidism.
The B1-TBII-bioassay as developed in our laboratory has a high sensitivity for the detection of TSAb in GD and predicts the severity of hyperthyroidism in untreated GD patients. In addition, we found that high TBII titres are associated with weak TSHR activation.
格雷夫斯病(GD)中的促甲状腺激素受体抗体(TBII)可能是促甲状腺激素受体刺激性(TSAb)抗体和阻断性(TBAb)抗体。然而,在市售检测方法中,只能测量总TBII滴度,无法区分TSAb和TBAb。
设计一种TBII生物测定法以检测TSAb,并将TSAb活性与初发GD患者甲状腺功能亢进的严重程度相关联。
35例初发GD患者和27例对照。
组成型表达促甲状腺激素受体(TSHR)的JP-26-26细胞系用环磷酸腺苷反应元件 - 荧光素酶构建体进行稳定转染。克隆B1在0.2 mU/l至50 mU/l牛促甲状腺激素范围内发光呈近似线性增加,用作TBII生物测定法。测定所有患者和对照血清中的TBII、游离T4和促甲状腺激素。
在35例GD患者血清中,TBII滴度与血清游离T4浓度无相关性。相反,用TBII生物测定法测得的TSHR刺激活性(发光)与血清游离T4水平之间存在强烈且高度显著的相关性(R = 0.80,P < 0.001)。有趣的是,在低TBII滴度时,发光/TBII比值范围较宽,而高TBII滴度与低程度的TSHR激活相关。TBII生物测定法还在自发发生甲状腺功能减退的GD患者中检测到TBAb。
我们实验室开发的B1-TBII生物测定法对GD中TSAb的检测具有高灵敏度,并可预测未经治疗的GD患者甲状腺功能亢进的严重程度。此外,我们发现高TBII滴度与弱TSHR激活相关。