Heijtink R A, Kruining J, Schalm S W, Masurel N
J Virol Methods. 1985 Apr;10(4):333-9. doi: 10.1016/0166-0934(85)90050-3.
Two assays for the detection of antibody against hepatitis B surface antigen (anti-HBs) were compared. The first was a direct sandwich radioimmunoassay (RIA) which detects, in principle, antibody against any epitope of hepatitis B surface antigen (HBsAg). The second assay was an inhibition enzyme-linked immunosorbent assay (ELISA). In this assay a fixed amount of HBsAg which can be blocked by anti-HBs is measured in a direct sandwich test. Prevaccination screening sera (n = 191) and follow-up sera obtained from high risk groups (n1 = 85; n2 = 41) during two hepatitis B vaccine studies were compared in RIA and ELISA. In prevaccination sera either HBsAg or anti-HBs were detected by ELISA. Full agreement between the results of RIA and ELISA for anti-HBs was obtained in sera containing more than 10 IU/l anti-HBs. Both tests showed variable results at low titres. Experiments with monoclonal anti-HBs indicated that ELISA is less sensitive for subtype specific antibodies (anti-d, anti-y), which may explain that there were consistent differences between RIA and ELISA in a minority of cases.
对两种检测乙型肝炎表面抗原抗体(抗-HBs)的检测方法进行了比较。第一种是直接夹心放射免疫测定法(RIA),原则上可检测针对乙型肝炎表面抗原(HBsAg)任何表位的抗体。第二种检测方法是抑制酶联免疫吸附测定法(ELISA)。在该测定法中,在直接夹心试验中测量可被抗-HBs阻断的固定量的HBsAg。在两项乙型肝炎疫苗研究期间,对预接种筛查血清(n = 191)以及从高危组获得的随访血清(n1 = 85;n2 = 41)进行了RIA和ELISA比较。在预接种血清中,通过ELISA检测到HBsAg或抗-HBs。在抗-HBs含量超过10 IU/l的血清中,RIA和ELISA检测抗-HBs的结果完全一致。两种检测方法在低滴度时均显示出可变结果。使用单克隆抗-HBs的实验表明,ELISA对亚型特异性抗体(抗-d、抗-y)的敏感性较低,这可能解释了在少数情况下RIA和ELISA之间存在一致差异的原因。