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Detection of anti-neuraminidase antibody in preclinical and clinical studies of live influenza vaccine

机译:实时流感疫苗的临床前和临床研究中抗神经氨酸酶抗体的检测

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The aim of this study is to evaluate antibody response to influenza virus neuraminidase (NA) following immunization with live attenuated influenza vaccine (LATV). We adjusted the peroxidase-linked lectin micro-procedure previously reported by Lambre, et al. (1990) to assay neuraminidase inhibition (NI) antibody in sera taken from immunized mice and from human subjects in a clinical trial. For the assay, we prepared the A(H7N1) reassortant virus containing the NA of A/California/07/2009 (H1N1) and the hemagglutinin (HA) of A/equine/Pra-gue/l/56(H7N7). In addition, we used an NA-specific IgG ELISA assay to test sera from immunized mice and volunteers. In mice, one dose of LAIV induced NI antibody of a geometric mean titer (GMT) of 31-7, compared to 10-6 in the control group. GMT of NI from human subjects who received two doses of pandemic A(H1N1) were significantly higher than pre-vaccination titers. In unvaccinated human subjects, NA-specific cross-reactive antibodies to pandemic A(H1N1) were detected more often than cross-reactive antibodies to HA.
机译:这项研究的目的是评估减毒活流感疫苗(LATV)免疫后对流感病毒神经氨酸酶(NA)的抗体反应。我们调整了Lambre等人先前报道的过氧化物酶连接的凝集素微过程。 (1990)在一项临床试验中测定从免疫小鼠和人类受试者获得的血清中的神经氨酸酶抑制(NI)抗体。对于测定,我们制备了含有A /加利福尼亚/ 2009/7/7 / Pra-gue / 1/56(H7N7)的NA和加利福尼亚的NA(H1N1)和血凝素(HA)的A(H7N1)重配病毒。此外,我们使用了NA特异性IgG ELISA试验来测试免疫小鼠和志愿者的血清。在小鼠中,一剂LAIV诱导的NI抗体的几何平均滴度(GMT)为31-7,而对照组为10-6。接受两次大流行A(H1N1)感染的人类受试者的NI GMT显着高于疫苗接种前的滴度。在未接种疫苗的人类受试者中,大流行性A(H1N1)的NA特异性交叉反应抗体比HA交叉反应抗体的检测频率更高。

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