Live attenuated pandemic influenza vaccine: Clinical studies on A/17/California/2009/38 (H1N1) and licensing of the Russian-developed technology to WHO for pandemic influenza preparedness in developing countries

被引:46
作者
Rudenko, Larisa [1 ,2 ]
van den Bosch, Han [3 ]
Kiseleva, Irina [1 ,2 ]
Mironov, Alexander [4 ]
Naikhin, Anatoly [1 ]
Larionova, Natalie [1 ]
Bushmenkov, Dimitry [4 ]
机构
[1] Inst Expt Med, Dept Virol, Sr Petersburg, Russia
[2] BioDiem Ltd, Melbourne, Vic, Australia
[3] Nobilon Int BV, Boxmeer, Netherlands
[4] Microgen Fed State Co, Moscow, Russia
关键词
Live attenuated influenza vaccine; Pandemic; Technology transfer; WHO; Clinical; CELLULAR IMMUNE-RESPONSES; INFECTION;
D O I
10.1016/j.vaccine.2011.04.122
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
In February 2009, Nobilon granted the World Health Organization (WHO) a non-exclusive licence to develop, register, manufacture, use and sell seasonal a pandemic live attenuated influenza vaccine (LAIV) produced on embryonated chicken eggs. WHO was permitted to grant sub-licences to vaccine manufacturers in developing countries within the framework of its influenza vaccine technology transfer initiative. In parallel, the Institute of Experimental Medicine (IEM), Russia, concluded an agreement with WHO for the supply of Russian LAIV reassortants for use by these manufacturers. Also in 2009, IEM carried out a study on a novel A/17/California/2009/38 (H1N1) pandemic LAIV candidate derived from the pandemic-related A/California/07/2009 (H1N1) influenza virus and the attenuated A/Leningrad/134/17/57 (H2N2) master donor virus, using routine reassortant technique in embryonated chicken eggs. Following successful preclinical studies in eggs and in ferrets, a double-blind, controlled, randomized clinical trial was carried out in immunologically naive study participants between 12-18 and 18-60 years old. Collectively, the immunogenicity data (haemagglutinin inhibition test, ELISA and cytokine tests for the detection of memory T cells) support the use of a single dose of the pandemic H1N1 LAIV in 12-60 year olds. The outcome of the studies showed no significant adverse reactions attributable to the vaccine, and suggests that the vaccine is as safe and immunogenic as seasonal influenza vaccines. Importantly, it was clearly demonstrated that reliance on the HAI assay alone is not recommended for testing LAIV. To date, via the licence agreement with WHO, the H1N1 LAIV has been transferred to the Government Pharmaceutical Organization in Thailand, the Serum Institute of India, and the Zhejiang Tianyuan Bio-Pharmaceutical Co., Ltd. in China. (C) 2011 Elsevier Ltd. All rights reserved.
引用
收藏
页码:A40 / A44
页数:5
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