Hanson M R, Polesky H F
Transfusion. 1987 Jan-Feb;27(1):107-8. doi: 10.1046/j.1537-2995.1987.27187121451.x.
Routine antibody to hepatitis B core antigen (anti-HBc) screening, recommended as a surrogate test to identify potential carriers of non-A, non-B hepatitis, was evaluated on 22,346 blood donors using currently available enzyme immunoassay (EIA) reagents. Of the 2 percent found reactive, the majority had cutoff-to-sample absorbance ratios less than 2.0 and less than one-half had anti-HBc when tested by a radioimmunoassay (RIA) method. Only one of 2877 units donated previously by the reactive donors was implicated in a transfusion associated hepatitis case. These results raise questions about the use of currently available anti-HBc reagents as a surrogate test for non-A, non-B hepatitis.
作为一种用于识别非甲非乙型肝炎潜在携带者的替代检测方法,常规乙肝核心抗原抗体(抗-HBc)筛查使用现有的酶免疫测定(EIA)试剂在22346名献血者中进行了评估。在检测出的2%反应性样本中,大多数样本的临界值与样本吸光度比值小于2.0,并且采用放射免疫测定(RIA)方法检测时,不到一半的样本含有抗-HBc。反应性献血者之前捐献的2877单位血液中,仅有1单位与1例输血相关肝炎病例有关。这些结果对将现有的抗-HBc试剂用作非甲非乙型肝炎的替代检测方法提出了质疑。