Liu Jia, Chen Lin, Xu Jju, Guo Jing-Xia, Song Yong-Ji, Zhao Jing, Liu Ai-Xia, Yang Li-Hua, Li Bo-An, Mao Yuan-Li
Center of Clinical Laboratory, The No. 302 Hospital of The PLA, Beijing 100039, China.
Zhonghua Shi Yan He Lin Chuang Bing Du Xue Za Zhi. 2011 Dec;25(6):492-4.
Establish a kind of confirmation method based on ELISA, and use to verify authenticity of HBsAb + in HBsAg + HBsAb + serum, pick and get rid of the false masculine gender the result, and avoid the mistake diagnosis.
Collect 60 pieces of serum whose thick degree of HBsAg at 1000 COI above tested by ECLIA as confirm serum, mixed the confirm serum of different dilution with HBsAb positive serum to screen and verify best thick degree of HBsAg. Collected 40 pieces of HBsAg + HBsAb + serum, ELISA tested the descend rate of HBsAb COI after neutralized with confirm serum in order to confirm authenticity of HBsAb + in pieces of HBsAg + HBsAb + serum.
When thick degree of HBsAg is 2000 COI, the performance of neutralization to HBsAb is best. The ELISA confirmatory test is fully consistent with the ECLIA method with true positive of 37 pieces of HBsAg + HBsAb + serum while false-positive of 3 pieces of serum.
The ELISA confirm method is a simple, accurate and low cost initial validation method.
建立一种基于酶联免疫吸附测定(ELISA)的确认方法,用于验证HBsAg+HbsAb+血清中HbsAb+的真实性,剔除假阳性结果,避免误诊。
收集60份经电化学发光免疫分析(ECLIA)检测HBsAg浓度在1000 COI以上的血清作为确认血清,将不同稀释度的确认血清与HbsAb阳性血清混合,筛选并验证最佳HBsAg浓度。收集40份HBsAg+HbsAb+血清,用确认血清中和后,通过ELISA检测HbsAb COI的下降率,以确认各份HBsAg+HbsAb+血清中HbsAb+的真实性。
当HBsAg浓度为2000 COI时,对HbsAb的中和性能最佳。ELISA确认试验与ECLIA方法完全一致,37份HBsAg+HbsAb+血清为真阳性,3份血清为假阳性。
ELISA确认方法是一种简单、准确且低成本的初步验证方法。