Chen Hualan, Subbarao Kanta, Swayne David, Chen Qi, Lu Xiuhua, Katz Jacqueline, Cox Nancy, Matsuoka Yumiko
Influenza Branch, Mailstop G-16, Centers for Disease Control and Prevention, 1600 Clifton Road, Atlanta, GA 30333, USA.
Vaccine. 2003 May 16;21(17-18):1974-9. doi: 10.1016/s0264-410x(02)00809-5.
H9N2 subtype avian influenza viruses (AIVs) are widely distributed in avian species and were isolated from humans in Hong Kong and Guangdong province, China in 1999 raising concern of their potential for pandemic spread. We generated a high-growth reassortant virus (G9/PR8) that contains the hemagglutinin (HA) and neuraminidase (NA) genes from the H9N2 avian influenza virus A/chicken/Hong Kong/G9/97 (G9) and six internal genes from A/Puerto Rico/8/34 (PR8) by genetic reassortment, for evaluation as a potential vaccine candidate in humans. Pathogenicity studies showed that the G9/PR8 reassortant was not highly pathogenic for mice or chickens. Two doses of a formalin-inactivated G9/PR8 virus vaccine induced hemagglutination inhibiting antibodies and conferred complete protection against challenge with G9 and the antigenically distinct H9N2 A/Hong Kong/1073/99 (G1-like) virus in a mouse model. These results indicate that the high growth G9/PR8 reassortant has properties that are desirable in a vaccine seed virus and is suitable for evaluation in humans for use in the event of an H9 pandemic.
H9N2亚型禽流感病毒(AIV)广泛分布于禽类中,1999年在中国香港和广东省从人类身上分离出该病毒,这引发了人们对其大流行传播潜力的担忧。我们通过基因重配产生了一种高生长重组病毒(G9/PR8),它含有来自H9N2禽流感病毒A/鸡/香港/G9/97(G9)的血凝素(HA)和神经氨酸酶(NA)基因以及来自A/波多黎各/8/34(PR8)的六个内部基因,用于评估其作为人类潜在疫苗候选物的可能性。致病性研究表明,G9/PR8重组病毒对小鼠或鸡不具有高致病性。两剂福尔马林灭活的G9/PR8病毒疫苗在小鼠模型中诱导产生了血凝抑制抗体,并对G9和抗原性不同的H9N2 A/香港/1073/99(G1样)病毒的攻击提供了完全保护。这些结果表明,高生长的G9/PR8重组病毒具有疫苗种子病毒所需的特性,适合在人类中进行评估,以备H9大流行时使用。