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Development of a new radioimmunoassay for erythropoietin using recombinant erythropoietin

机译:使用重组促红细胞生成素开发一种新的促红细胞生成素放射免疫测定方法

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Development of a new radioimmunoassay for erythropoietin using recombinant erythropoietin. The development of a 24 hour radioimmunoassay for erythropoietin (EPO) using EPO derived from recombinant DNA as both immunogen and ligand is described in the present paper. Mixed breed rabbits immunized with 10 g/kg of EPO derived from a stably transfected cell line (Elanex Pharmaceuticals Inc., Bothel, Washington, USA, through McDonnell Douglas Corp., St. Louis, Missouri, USA; "MD") produced antibodies to EPO with high titer (up to 1:896,000 final dilution in the tube), high affinity (8.4 1011 liter/M), and good specificity. Purified EPO from the above source or from AmGen Biologicals (Thousand Oaks, California, USA; "AG") were successfully radioiodinated with the chloramine-T method and used as ligand in the radioimmunoassay. Standard dose-response curves prepared with EPO from both commercial sources were not significantly different and showed a sensitivity of 0.75 to 0.96 mU/tube. The dose-response curves in both systems also showed parallelism with serially diluted serum from a patient with aplastic anemia. Within-assay and between-assay precision were determined by assaying multiple replicates of a serum pool. Recovery of exogenous EPO added to a serum pool averaged 97% for both systems. The range of normal human serum EPO was determined by assaying the sera of 153 hematologically-normal adult subjects and was found to be 1.1 to 27.3 mU/ml for MD EPO and 0.5 to 16.7 mU/ml for AG EPO. Sera from several patients with hematologic abnormalities were also assayed, including those of 36 patients with anemia of end-stage renal disease (mean SEM, 29.5 4.0 mU/ml; P < 0.01). In conclusion, this new, more rapid and sensitive radioimmunoassay system can be used to measure EPO levels in sera from normal human subjects and patients with several types of anemia, and should also be very useful in therapeutic drug monitoring of patients receiving EPO from various commercial sources.
机译:使用重组促红细胞生成素开发一种新的促红细胞生成素放射免疫测定方法。本文描述了使用衍生自重组DNA的EPO作为免疫原和配体的促红细胞生成素(EPO)24小时放射免疫分析方法的开发。用源自稳定转染的细胞系(Elanex Pharmaceuticals Inc.,美国华盛顿州博塞尔,通过McDonnell Douglas Corp.,美国密苏里州,美国;“ MD”)的10 g / kg EPO免疫的混种兔产生抗体具有高滴度(在试管中最终稀释度可达1:896,000),高亲和力(8.4 1011升/ M)和良好的特异性。从上述来源或从AmGen Biologicals(美国加利福尼亚州千橡市,“ AG”)获得的纯化EPO已成功通过氯胺T方法进行了放射性碘标记,并在放射免疫分析中用作配体。两种商业来源的EPO制备的标准剂量反应曲线均无显着差异,灵敏度为0.75至0.96 mU /管。在两个系统中的剂量反应曲线也显示出与再生障碍性贫血患者的系列稀释血清的平行性。通过测定血清池的多个重复测定来测定测定内和测定间的精度。对于两个系统,添加到血清库中的外源性EPO的回收率平均为97%。正常人血清EPO的范围是通过测定153名血液学正常的成年人的血清来确定的,发现MD EPO为1.1至27.3 mU / ml,AG EPO为0.5至16.7 mU / ml。还测定了几例血液学异常患者的血清,包括36例终末期肾脏疾病贫血患者的血清(平均SEM,29.5 4.0 mU / ml; P <0.01)。总之,这种新型,更快速,更灵敏的放射免疫分析系统可用于测量正常人和几种贫血患者血清中的EPO水平,对于从各种商业渠道接受EPO的患者的治疗药物监测也应非常有用。资料来源。

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