Bradley D W, Fields H A, McCaustland K A, Maynard J E, Decker R H, Whittington R, Overby L R
J Clin Microbiol. 1979 Jan;9(1):120-7. doi: 10.1128/jcm.9.1.120-127.1979.
A competitive binding radioimmunoassay (CBA) for antibody to hepatitis A virus (HAV) was evaluated and compared with a standard solid-phase radioimmunoassay for anti-HAV, CBA was found to be sensitive and specific for the detection of anti-HAV, as demonstrated by the 98% concordance of CBA and solid-phase radioimmunoassay test results. The standard CBA test was modified for the differential detection of acute (immunoglobulin M) and convalescent (immunoglobulin G) anti-HAV by incorporation of a step in which immunoglobulin G anti-HAV was preferentially absorbed with S. aureus cells (protein A). The modified CBA test was shown to be capable of differentiating between acute- and convalescent-phase sera. The modified CBAM test was able to detect immunoglobulin M anti-HAV up to approximately 4 weeks after the onset of illness.
对甲型肝炎病毒(HAV)抗体的竞争性结合放射免疫测定(CBA)进行了评估,并与抗-HAV的标准固相放射免疫测定进行了比较。发现CBA在检测抗-HAV方面具有敏感性和特异性,CBA与固相放射免疫测定测试结果的一致性为98%,证明了这一点。通过加入一步,其中抗-HAV免疫球蛋白G被金黄色葡萄球菌细胞(蛋白A)优先吸收,对标准CBA试验进行了改进,用于急性(免疫球蛋白M)和恢复期(免疫球蛋白G)抗-HAV的鉴别检测。改进后的CBA试验能够区分急性期和恢复期血清。改进后的CBAM试验能够在发病后约4周内检测到抗-HAV免疫球蛋白M。