Panteghini M, Bonora R, Pagani F
1st Laboratorio Analisi Chimico-Cliniche, Settore di Chimica Clinica ed Enzimologia, Spedali Civili, Brescia, Italy.
Eur J Clin Chem Clin Biochem. 1994 May;32(5):383-9. doi: 10.1515/cclm.1994.32.5.383.
We report a preliminary evaluation of an immunoinhibition assay for creatine kinase isoform quantification. The procedure employs the monoclonal antibody CKM-G01, which inhibits the native M subunit of creatine kinase. The antibody does not inhibit the M subunit modified by removal of lysine by plasma carboxypeptidase N. Residual activity after treatment with the antibody is therefore due to serum delysinated isoforms. The ratio inhibited/residual activity correlated directly with the ratio tissue/serum isoforms. Analysis of the total imprecision of isoform ratio measurement gave a coefficient of variation between 5.9 and 21.1%. Reference intervals for the ratio were 0.14-0.79 in females and 0.19-0.95 in men (p = 0.0046). Analytical and clinical comparison with alternative isoform procedures gave good results, showing that this assay can be used as alternative to the widely accepted electrophoretic method for measurement of the creatine kinase isoform ratio.
我们报告了一种用于肌酸激酶同工酶定量的免疫抑制测定法的初步评估。该方法采用单克隆抗体CKM-G01,它可抑制肌酸激酶的天然M亚基。该抗体不会抑制经血浆羧肽酶N去除赖氨酸修饰后的M亚基。因此,用该抗体处理后的残余活性归因于血清去赖氨酸同工酶。抑制活性/残余活性的比率与组织/血清同工酶的比率直接相关。对同工酶比率测量的总不精密度分析得出变异系数在5.9%至21.1%之间。该比率的参考区间在女性中为0.14 - 0.79,在男性中为0.19 - 0.95(p = 0.0046)。与其他同工酶检测方法进行的分析和临床比较结果良好,表明该测定法可作为广泛接受的电泳法的替代方法用于测量肌酸激酶同工酶比率。