Kashiwagi S, Hayashi J, Noguchi A, Nakashima K, Hirata M, Kajiyama W
Department of General Medicine, Kyushu University Hospital.
Kansenshogaku Zasshi. 1992 Mar;66(3):390-9. doi: 10.11150/kansenshogakuzasshi1970.66.390.
A fully automated microparticle enzyme immunoassay (IMx AUSAB, Abbott) has been recently introduced for the detection of the presence of antibody to hepatitis B surface antigen (anti-HBs). The present trial was carried out to determine the feasibility of using the IMx AUSAB with sera and plasma, and for comparison with RIA (AUSAB, Abbott) and EIA (AUSAB EIA, Abbott). According to the kinds of vaccines used and locations of residents, the subjects were divided into six groups. Results obtained were as follows; In the test of 642 sera from 446 vaccines and 196 other inhabitants of Okinawa and Miyazaki prefectures, 388 (87.0%) were found positive for anti-HBs using IMx, 392 (87.9%) with RIA and 359 (80.5%) with EIA. Among those vaccinated with recombinant vaccines, 96.6% were found positive with IMx, 96.2% with RIA and 89.4% with EIA. Among subject vaccinated with plasma derived vaccines, 72.9% were found positive with IMx, 75.7% with RIA, and 68.5% EIA. Quantitative agreement between IMx and RIA among the six groups gave linear correlation coefficients ranging from 0.459 to 0.821. In the group vaccinated with the recombinant vaccine by K company (r = 0.459), anti-HBs was confirmed in many sera by IMx compared to that confirmed by RIA and EIA. In addition, anti-HBs was assayed within one hour by IMx and the procedure was simplified by autoanalyser equipped for this method. The results indicate that the sensitivity of IMx is equal to that of RIA and more than that of EIA, and that quantitative linear correlations were obtained between IMx and RIA, and IMx and EIA.
最近推出了一种全自动微粒酶免疫测定法(IMx AUSAB,雅培公司)用于检测乙型肝炎表面抗原抗体(抗-HBs)的存在。本试验旨在确定IMx AUSAB用于血清和血浆检测的可行性,并与放射免疫测定法(RIA,AUSAB,雅培公司)和酶免疫测定法(EIA,AUSAB EIA,雅培公司)进行比较。根据所使用疫苗的种类和居民所在地区,将受试者分为六组。得到的结果如下:在对来自冲绳县和宫崎县的446名接种疫苗者和196名其他居民的642份血清进行检测时,使用IMx法发现388份(87.0%)抗-HBs呈阳性,RIA法为392份(87.9%),EIA法为359份(80.5%)。在接种重组疫苗的人群中,IMx法检测到96.6%呈阳性,RIA法为96.2%,EIA法为89.4%。在接种血浆源性疫苗的受试者中,IMx法检测到72.9%呈阳性,RIA法为75.7%,EIA法为68.5%。六组中IMx与RIA之间的定量一致性给出的线性相关系数范围为0.459至0.821。在由K公司生产的重组疫苗接种组(r = 0.459)中,与RIA法和EIA法相比,IMx法在许多血清中检测到更多的抗-HBs。此外,IMx法在一小时内即可完成抗-HBs检测,并且配备该方法的自动分析仪简化了检测程序。结果表明,IMx的灵敏度与RIA相当且高于EIA,并且在IMx与RIA以及IMx与EIA之间获得了定量线性相关性。