Tsai C C, Yarnall M, Follis K E, Benveniste R E
Regional Primate Research Center, University of Washington, Seattle 98195.
Lab Anim Sci. 1989 Nov;39(6):554-9.
A rapid, sensitive and specific antigen capture (AC) assay has been established for the detection of p27 core protein of SAIDS type-D retrovirus (SRV). SRV p27 antigen in test samples was identified on rabbit anti-p27 IgG-coated microtiter plates by the addition of biotinylated rabbit anti-p27 IgG. This assay was specific for the p27 core protein of SRV-1 and SRV-2 and provided semi-quantitative results in less than 7 hours. Results of the AC assay were highly correlated with those of reverse transcriptase (RT), immunofluorescence and immunoblotting assays. However, the AC assay was faster and more sensitive than the other three assays. The AC assay also provided a rapid diagnostic tool for the detection of SRV in plasma, serum and peripheral blood lymphocyte cocultures. In addition to mass screening of SRV infection in macaque colonies, the AC assay also will be valuable for monitoring the efficacy of antiretroviral agents against SRV in vitro and in vivo.
已建立一种快速、灵敏且特异的抗原捕获(AC)检测法,用于检测猴艾滋病D型逆转录病毒(SRV)的p27核心蛋白。通过在兔抗p27 IgG包被的微量滴定板上加入生物素化的兔抗p27 IgG,来鉴定测试样品中的SRV p27抗原。该检测法对SRV-1和SRV-2的p27核心蛋白具有特异性,且在不到7小时内提供半定量结果。AC检测法的结果与逆转录酶(RT)、免疫荧光和免疫印迹检测法的结果高度相关。然而,AC检测法比其他三种检测法更快且更灵敏。AC检测法还为检测血浆、血清和外周血淋巴细胞共培养物中的SRV提供了一种快速诊断工具。除了对猕猴群体中的SRV感染进行大规模筛查外,AC检测法对于监测抗逆转录病毒药物在体外和体内针对SRV的疗效也将具有重要价值。