Wu J T, Wilson L, Zhang P, Meikle A W, Stephenson R
Department of Pathology, University of Utah School of Medicine, Salt Lake City, USA.
J Clin Lab Anal. 1995;9(1):15-24. doi: 10.1002/jcla.1860090103.
The current assays for serum prostate specific antigen (PSA) have failed to produce the same PSA values on the same specimens because of problems with antibody specificity and calibrator preparation. To eliminate these problems, we proposed to replace the current serum PSA assay with an assay specific for the PSA-ACT (PSA-alpha 1-antichymotrypsin) complex in the serum. An assay specific for the PSA-ACT complex was established using the anti-PSA antibody to coat the microplate for capturing the PSA complex and anti-ACT polyclonal antibodies for quantification. There was an excellent correlation between serum concentrations of PSA-ACT and total PSA, using either the Hybritech calibrator (gamma = 0.996) or a serum calibrator prepared in house (gamma = 0.993), in random as well as in serial specimens from 14 individual patients. Even though we did not find a gradual increase in the percentage of PSA-ACT with the increase of total PSA in cancer patients, a slightly higher percentage of free PSA was measured in pooled normal sera (18%) and in pooled sera containing only 12 ng/ml of total PSA (12%), compared to serum pools containing elevated PSA (> 100 ng/ml) level, in which most PSA was in the complex form (95%). Therefore, using an assay that specifically measures the PSA-ACT complex in the serum not only simplifies the preparation of calibrator but eliminates the difficulty of antibody selection, it also allows various assay kits to produce identical PSA values and also improve the test specificity for prostate cancer.
由于抗体特异性和校准品制备方面的问题,目前用于检测血清前列腺特异性抗原(PSA)的方法在相同标本上无法得出相同的PSA值。为消除这些问题,我们提议用一种针对血清中PSA-ACT(PSA-α1-抗糜蛋白酶)复合物的检测方法取代当前的血清PSA检测方法。通过使用抗PSA抗体包被微孔板以捕获PSA复合物,并使用抗ACT多克隆抗体进行定量,建立了一种针对PSA-ACT复合物的检测方法。在14名个体患者的随机及系列标本中,无论是使用Hybritech校准品(γ = 0.996)还是自制的血清校准品(γ = 0.993),PSA-ACT的血清浓度与总PSA之间均存在极好的相关性。尽管我们未发现癌症患者中PSA-ACT的百分比随总PSA的增加而逐渐升高,但与PSA水平升高(> 100 ng/ml)的血清池相比,在混合正常血清(18%)和仅含12 ng/ml总PSA的混合血清(12%)中测得的游离PSA百分比略高,在PSA水平升高的血清池中,大多数PSA处于复合物形式(95%)。因此,使用一种专门检测血清中PSA-ACT复合物的检测方法不仅简化了校准品的制备,消除了抗体选择的困难,还能使各种检测试剂盒得出相同的PSA值,并提高前列腺癌检测的特异性。