Ferguson R A, Yu H, Kalyvas M, Zammit S, Diamandis E P
Department of Pathology and Laboratory Medicine, Mount Sinai Hospital, Toronto, ON, Canada.
Clin Chem. 1996 May;42(5):675-84.
We report an ultrasensitive time-resolved immunofluorometric assay (TRIFA) for prostate-specific antigen (PSA). The assay is an improvement of our previous report (Clin Chem 1993;39:2108-14) and includes the utilization of two monoclonal antibodies and a one-step incubation period, which greatly reduces analysis time. The new method demonstrates a superior lower analytical limit of detection (< or = 1 ng/L), a wide dynamic range, absence of a hook effect at 10(6) ng/L PSA, and equimolarity for free PSA and PSA-antichymotrypsin complex. Also, we have compared several aspects of our TRIFA with a commercially available third-generation assay (Immulite). An evaluation of breast tumor cytosol extracts from 315 patients shows PSA immunoreactivity > 15 ng/g of total protein in 28% and 23% by TRIFA and Immulite analysis, respectively. Both methods demonstrate a significant association between breast tumor PSA immunoreactivity and progesterone and estrogen receptor positivity (P <0.001). Analysis of serum samples obtained for monitoring of postradical prostatectomy patients reveals significant PSA changes at concentrations undetectable by conventional methods. The significance of these results as well as the potential applications of ultrasensitive PSA assays in breast and prostate cancers are discussed.
我们报告了一种用于前列腺特异性抗原(PSA)的超灵敏时间分辨免疫荧光测定法(TRIFA)。该测定法是对我们之前报告(《临床化学》1993年;39卷:2108 - 2114页)的改进,包括使用两种单克隆抗体和一步温育期,这大大缩短了分析时间。新方法显示出卓越的较低分析检测限(≤1 ng/L)、宽动态范围、在10⁶ ng/L PSA时无钩状效应,以及游离PSA和PSA - 抗糜蛋白酶复合物的等摩尔性。此外,我们将我们的TRIFA的几个方面与一种市售的第三代测定法(免疫发光分析仪)进行了比较。对315例患者的乳腺肿瘤胞质溶胶提取物进行评估,通过TRIFA和免疫发光分析仪分析,分别有28%和23%的提取物显示PSA免疫反应性>15 ng/g总蛋白。两种方法均显示乳腺肿瘤PSA免疫反应性与孕酮和雌激素受体阳性之间存在显著关联(P<0.001)。对用于监测前列腺癌根治术后患者的血清样本进行分析,发现在常规方法无法检测到的浓度下PSA有显著变化。讨论了这些结果的意义以及超灵敏PSA测定法在乳腺癌和前列腺癌中的潜在应用。