Schüpbach J, Böni J
Swiss National Center for Retroviruses, Institute of Medical Virology, University of Zurich.
J Virol Methods. 1993 Jul;43(2):247-56. doi: 10.1016/0166-0934(93)90080-b.
5-min boiling of 3-fold diluted serum leads to the quantitative release of immune-complexed HIV antigen (Ag) that can be readily measured. The method is capable of detecting as little as 4 to 5 pg/ml Ag p24 depending on the Ag test used. Of a panel of 50 anti-HIV-positive sera, 30 (60%) were Ag-positive after heat denaturation, 17 (34%; P < or = 0.01) after acidification, and 13 (26%; P < or = 0.001) when tested undenatured. The superiority of heat denaturation was greatest in sera with high-titered antibodies to p24. Occurrence and mean concentrations of heat-denatured Ag were reversely correlated with p24-specific antibody. It is suggested that heat-denatured proteins be used for raising antibodies that will serve as capture or trace antibodies in Ag assays. This simple change in the manufacturing of test reagents in combination with a short boil before testing may solve the problem of incomplete Ag detection due to immune complex formation.
将三倍稀释的血清煮沸5分钟可使免疫复合物中的HIV抗原(Ag)定量释放,且易于检测。根据所使用的抗原检测方法,该方法能够检测低至4至5 pg/ml的p24抗原。在一组50份抗HIV阳性血清中,30份(60%)在热变性后呈抗原阳性,17份(34%;P≤0.01)在酸化后呈阳性,13份(26%;P≤0.001)在未变性检测时呈阳性。热变性的优势在针对p24的高滴度抗体血清中最为明显。热变性抗原的出现率和平均浓度与p24特异性抗体呈负相关。建议使用热变性蛋白来制备抗体,这些抗体可作为抗原检测中的捕获抗体或示踪抗体。检测试剂生产过程中的这一简单改变,再加上检测前短时间煮沸,可能会解决因免疫复合物形成导致抗原检测不完全的问题。