Kiyohara Tomoko, Ouchi Yoshimi, Hasegawa Yoshiko, Sato Tomoko, Yoneyama Tetsuo, Ishii Koji, Ito Toshihiro, Wakita Takaji
Department of Virology II, National Institute of Infectious Diseases, Tokyo, Japan.
J Med Virol. 2009 Sep;81(9):1513-6. doi: 10.1002/jmv.21578.
An anti-hepatitis A virus (HAV)-specific immunoglobulin M capture enzyme-linked immunosorbent assay (anti-HAV IgM ELISA) kit was re-designed for laboratory use and compared with a commercial anti-HAV IgM detection system using 58 serum samples collected from patients, vaccines, and healthy individuals. Because concordance between the two systems was high (r = 0.93, P < 0.05), 19 sets of serum and fecal samples obtained from individuals exposed to an HAV outbreak were also examined. Serum levels of anti-HAV IgM were determined using the in-house ELISA kit and the HAV genome in fecal samples was detected using the polymerase chain reaction (PCR). Among the 19 sets of sample, 14 were positive for both anti-HAV IgM and the HAV genome. All of those whose serum samples were anti-HAV IgM negative were also negative for the HAV genome in fecal samples. The results of the in-house IgM ELISA were consistent with those of the HAV genome detected by PCR and with the commercial IgM ELISA. The in-house anti-HAV IgM ELISA kit was therefore proven suitable for laboratory use and applicable to epidemiological studies of HAV infection.
一种抗甲型肝炎病毒(HAV)特异性免疫球蛋白M捕获酶联免疫吸附测定(抗HAV IgM ELISA)试剂盒被重新设计用于实验室,并与一种商用抗HAV IgM检测系统进行比较,该比较使用了从患者、疫苗接种者和健康个体收集的58份血清样本。由于两种系统之间的一致性很高(r = 0.93,P < 0.05),因此还对从暴露于甲型肝炎病毒爆发的个体获得的19组血清和粪便样本进行了检测。使用自制ELISA试剂盒测定血清中抗HAV IgM水平,并使用聚合酶链反应(PCR)检测粪便样本中的HAV基因组。在这19组样本中,14组抗HAV IgM和HAV基因组均呈阳性。所有血清样本抗HAV IgM阴性的个体,其粪便样本中的HAV基因组也为阴性。自制IgM ELISA的结果与PCR检测的HAV基因组结果以及商用IgM ELISA的结果一致。因此,自制抗HAV IgM ELISA试剂盒被证明适用于实验室使用,并适用于甲型肝炎病毒感染的流行病学研究。