摘要
目的 建立更敏感的检测人免疫缺陷病毒 (HIV)抗体的方法 ,并研制检测试剂盒。方法 根据HIV 1/2型的基因序列及其所编码氨基酸结构 ,采用固相法合成了HIV 1型的 gp41.1、gp41.2、gp12 0、p2 4和HIV 2型的 gp36五条多肽 ,混合包被酶标板作为固相抗原。用辣根过氧化物酶标记以上多肽抗原作为标记物 ,建立检测血清中抗HIV 1/2抗体的双抗原夹心ELISA法。同时 ,应用该方法制备检测HIV抗体的试剂盒 ,并检测三批中国卫生部药品和生物制品检定所HIV诊断试剂国家参比品。结果 建立了检测HIV 1/2抗体的双抗原夹心法。用检定所参比品检测 ,该方法特异性、灵敏度均为 10 0 % ,变异系数小于 10 %。与间接法相比较其灵敏度、特异性均高于间接法 (P<0 0 5 )。检测 2 10份其他病种患者血清均为阴性。与GBI公司的HIV抗体诊断试剂比较 ,检测 40份卫生部药品和生物制品检定所提供的质控参比品 (阳性 2 0份 ,阴性 2 0份 ) ,GBI试剂阴、阳性符合率及总符合率分别为 10 0 % (2 0 /2 0 )、85 % (17/2 0 )及 92 5 % (37/4 0 ) ,而应用该方法所研制的诊断试剂盒阴、阳性符合率及总符合率为 10 0 %。该试剂已通过国家卫生部质检。与雅培公司HIV诊断试剂比较检测 90份献血员血清和 88份HIV 1/2型感染者血清 ,符合率为 10 0 %。?
Objective To establish a sensitive antigen sandwiched ELISA(AS) for detection of the total antibodies to HIV 1/2.Methods Based on the gene sequence of HIV 1/2 type and its coded amino acid structure,5 polypeptides were synthesized as coated antigens using solid phase method. These polypeptides were labelled with horseradish peroxidase. And the total antibodies of HIV 1/2 were detected with the same method. Results These reagents were detected by three batches of HIV panel from The National Institute for the Control of Pharmaceutical and Biological Products (NICPBP). The results indicated that the corresponding rate was 100%. The variant coefficient rate was less than 10%. A comparison of antigen sandwiched ELISA with indirect ELISA in detection of a panel(20 positive sera and 20 negative sera) from the NICPBP showed that the general coincident rate of indirect ELISA was 92.5% and the sandwiched system was 100%. The HIV AS diagnostic reagent kits have passed the quality examination of NICPBP. A comparison of antigen sandwiched ELISA with Yapei reagents in detection of 90 normal sera and 88 positive sera for HIV 1/2 showed that the coincident rate was 100%. The reagents were stable at 37 ℃ for 4 days. This indicated that our reagents were highly specific,sensitive and stable. Conclusion Our antigen sandwiched ELISA reagent for total antibodies of HIV has a merit of sensitivity specificity and stability. It can be clinically used for detection of HIV 1/2 infection and in blood bank for the screening of blood donors.
出处
《中华实验和临床病毒学杂志》
CAS
CSCD
北大核心
2001年第1期43-46,共4页
Chinese Journal of Experimental and Clinical Virology