Lenzi M, Cassani F, Bianchi F B, Franceschi C
J Immunol Methods. 1983 Feb 25;57(1-3):59-69. doi: 10.1016/0022-1759(83)90065-0.
A microELISA to detect anti-liver-specific protein (LSP) antibodies in human sera is described. Rabbit LSP was used as antigen. Optimal conditions for antigen concentration, serum dilution, substrate incubation time and reproducibility with time were established. The microELISA is specific, as assessed by testing anti-LSP positive sera with another lipoprotein from rabbit plasma (VLDL), although a weak cross-reactivity between LSP and VLDL was observed. The test was applied to patients with HBsAg-positive and -negative chronic active hepatitis (CAH). Ten of 26 (38%) patients were positive for anti-LSP antibodies, in comparison with healthy controls used to determine the threshold of positivity. Such a percentage is comparable with that reported for radioimmunoassay (RIA) procedures.
本文描述了一种用于检测人血清中抗肝特异性蛋白(LSP)抗体的微量酶联免疫吸附测定法(microELISA)。兔LSP用作抗原。确定了抗原浓度、血清稀释度、底物孵育时间以及随时间变化的重现性的最佳条件。通过用兔血浆中的另一种脂蛋白(极低密度脂蛋白,VLDL)检测抗LSP阳性血清来评估,该微量酶联免疫吸附测定法具有特异性,不过观察到LSP与VLDL之间存在微弱的交叉反应。该检测方法应用于乙肝表面抗原(HBsAg)阳性和阴性的慢性活动性肝炎(CAH)患者。与用于确定阳性阈值的健康对照相比,26例患者中有10例(38%)抗LSP抗体呈阳性。该百分比与放射免疫测定法(RIA)程序报告的百分比相当。