Dai J, Dent W, Atkinson J W, Cox J G, Dembinski T C
Department of Clinical Chemistry, Health Sciences Centre, Winnipeg, Manitoba, Canada.
Clin Biochem. 1996 Oct;29(5):461-5. doi: 10.1016/0009-9120(96)00066-5.
This study describes the evaluation of performance of three immunoassay kits [Sanofi-Pasteur, IRMA, with five monoclonal antibodies; Wallac-Delfia, FIA, with double monoclonal antibodies; and Diagnostic Products Corporation (DPC), RIA, with polyclonal antibodies] for serum thyroglobulin in patients with thyroid cancer. Specific aims were (a) to recognize a method with minimal interference, by comparing analyte recoveries, from thyroglobulin autoantibodies (TgAb) that can be present in some thyroid cancer patient samples, (b) to correlate individual results with those from Mayo Medical Laboratories (MML) (current referred out assay service used by our institute), and (c) to compare assay precision.
In evaluating performance of the three immunoassays, procedures were followed as recommended by the respective manufacturers. Parallel comparison of the three immunoassays with the MML procedure was performed with thyroid cancer patient sera. Recovery studies utilized sera from 15 thyroid cancer patients, 4 Hashimoto's thyroiditis patients, and 1 Grave's disease patient. TgAb were also measured directly by an IRMA thyroglobulin antibody kit (Sanofi-Pasteur).
Among the randomly selected 20 samples assayed in parallel studies, low recoveries (< 80%) were present in 2 samples by IRMA assay (Sanofi-Pasteur), 8 samples by FIA assay (Wallac-Delfia), and 10 samples by RIA assay (DPC). The majority of the low recovery samples contained high titers of TgAb. All three kits correlated well with the Mayo method. At the control-1 level (approximately 9.9 microgram/L by Delfia determination), both the IRMA kit (CV = 1.96%, n = 10) and FIA Kit (CV = 2.16%, n = 10) showed good within-run precision.
In our hands, the IRMA Kit (Sanofi-Pasteur) demonstrated excellent precision, analyte recoveries, the least interference from TgAb, and good correlation with the Mayo Medical Laboratories procedure.
本研究描述了对三种免疫分析试剂盒[赛诺菲-巴斯德公司的免疫放射分析(IRMA)试剂盒,含五种单克隆抗体;瓦里安公司的时间分辨荧光免疫分析(FIA)试剂盒,含双单克隆抗体;以及诊断产品公司(DPC)的放射免疫分析(RIA)试剂盒,含多克隆抗体]在甲状腺癌患者血清甲状腺球蛋白检测中的性能评估。具体目标为:(a)通过比较分析物回收率,识别出受甲状腺球蛋白自身抗体(TgAb)干扰最小的方法,TgAb可能存在于部分甲状腺癌患者样本中;(b)将各试剂盒检测结果与梅奥医学实验室(MML)(我院目前使用的外部检测服务)的结果进行关联;(c)比较各试剂盒的检测精密度。
在评估这三种免疫分析方法的性能时,按照各制造商推荐的程序进行操作。使用甲状腺癌患者血清对这三种免疫分析方法与MML方法进行平行比较。回收研究使用了15例甲状腺癌患者、4例桥本甲状腺炎患者和1例格雷夫斯病患者的血清。TgAb也通过免疫放射分析甲状腺球蛋白抗体试剂盒(赛诺菲-巴斯德公司)直接检测。
在平行研究中随机选取的20份样本检测中,免疫放射分析(IRMA)试剂盒(赛诺菲-巴斯德公司)检测的2份样本、时间分辨荧光免疫分析(FIA)试剂盒(瓦里安公司)检测的8份样本以及放射免疫分析(RIA)试剂盒(DPC)检测的10份样本出现低回收率(<80%)。大多数低回收率样本含有高滴度的TgAb。所有三种试剂盒与梅奥方法的相关性都很好。在对照1水平(通过瓦里安检测约为9.9微克/升),免疫放射分析(IRMA)试剂盒(CV = 1.96%,n = 1)和时间分辨荧光免疫分析(FIA)试剂盒(CV = 2.16%,n = 1)均显示出良好的批内精密度。
在我们的研究中,免疫放射分析(IRMA)试剂盒(赛诺菲-巴斯德公司)表现出卓越的精密度、分析物回收率、受TgAb干扰最小,且与梅奥医学实验室的方法相关性良好。