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作 者:蒋雷[1] 国汉邦[1] 赵满仓[1] 刘菊林[1] 李健斋[1]
出 处:《中华医学检验杂志》1995年第3期136-139,共4页
摘 要:为建立特异有效的脂蛋白(a)检测方法,应用杂交瘤技术,制备出4株抗载脂蛋白(a)单克隆抗体,分别命名为M_1、M_2、M_3、M_4。各株单克隆抗体与纤溶酶原和载脂蛋白B等无交叉反应。单抗相加试验及竞争抑制试验结果表明:M_1、M_4识别同一抗原位点,M_2、M_3识别另一位点。选用M_1、M_2、M_43株单克隆抗体建立了测定血清脂蛋白(a)浓度的双抗体夹心酶联免疫测定法。样品稀释后测定范围为0.05~1.60mg/L,批内平均变异系数(CV)4.2%,批间平均CV8.7%。测定了1032例中老年临床血清标本,脂蛋白(a)浓度为179,1±179.3mg/L(x±s)。与多克隆抗体的酶联免疫测定法同时测定了38份临床标本,结果相似。此法可满足临床脂蛋白(3)浓度检测的需要。our clones of hybridoma which secreted monoclonal antibodies named as M_1、M_2、M_3 and M_4 to apolipoprotein(a)were developed.These monoclonal antibodies showed no cross-reaction to apolipopro-tein B and plasminogen. Immunologically,the M_1 and M_4 recognized the same antigenic epitope,where-as M_2 and M_3 recognized another. A sandwich enzyme-linked immunosorbent assay was established for determining serum lipoprotein(a)concentration with mixed McAbs (M_1、M_2 and M_4).The quantitative range is 0. 05~1. 60mg/L. The average intra-and inter-assay coefficient of variation were 4.2%and 8.7%respectively. The sera concentration of Lp(a ) in 103 2 middle-aged and old patients were mea-sured,and the result was 179.1±179.3mg/L.The results of this assay corresponded well to that of the ELISA method using polycolonal antibody to apolipoprotein(a).We concluded that this method was suitable for routine usage in clinical laboratories.
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