Pagani Sara, Chaler Eduardo A, Meazza Cristina, Maceiras Mercedes, Gonzalez Maria Eugenia, Rivarola Marco A, Cantoni Francesca, Travaglino Paola, Della Croce Lucia, Laarej Kamilia, Bozzola Mauro, Belgorosky Alicia
Pediatric Department, University ofPavia, Italy.
J Pediatr Endocrinol Metab. 2010 Aug;23(8):783-8. doi: 10.1515/jpem.2010.128.
We analyzed the ability of the BaF3 cell line bioassay to select patients with biologically inactive GH. We first evaluated the biological response of the Ba/F3-hGHR cells to rhGH additional doses from 10 to 5000 pg/ml. The concentration points corresponding to the linear part of the curve were selected. We then analyzed a group of sera, diluted like the standard, including the entire range of GH concentrations that can be analyzed by bioassay. The serum/standard area below the curve ratio was calculated. Serum GH immunoactivity determined by IMMULITE/GH bioactivity ratios was calculated. Our experimental data showed that GH-bioactivity/GH-immunoactivity ratios below 0.303 are indicative of a bioinactive GH molecule. This bioassay would recognize only extreme cases of GH bioinactivity, and it would not be a useful tool in the search for patients with altered forms of GH.
我们分析了BaF3细胞系生物测定法筛选出生长激素(GH)生物学活性缺失患者的能力。我们首先评估了Ba/F3-hGHR细胞对10至5000 pg/ml不同剂量重组人生长激素(rhGH)的生物学反应。选取了曲线线性部分对应的浓度点。然后我们分析了一组像标准品一样稀释的血清,包括生物测定法可分析的整个生长激素浓度范围。计算曲线下血清/标准品面积比。计算通过免疫发光法(IMMULITE)/生长激素生物活性比测定的血清生长激素免疫活性。我们的实验数据表明,生长激素生物活性/生长激素免疫活性比值低于0.303表明生长激素分子具有生物学活性缺失。这种生物测定法只能识别生长激素生物学活性缺失的极端情况,在寻找生长激素形式改变的患者方面并非有用的工具。