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诺华、诺瓦瓦克斯均开始研究禽流感疫苗


现代畜牧网 http://www.cvonet.com 2013/11/18 22:52:43 关注:501 评论: 我要投稿

  2013年11月17日讯 /生物谷BIOON/ --随着今年H7N9在中国再次出现,世界各国政府、人民对禽流感疫情再次爆发的担忧也越来越大。最近世界上两家主要疫苗生产商诺华公司和诺瓦瓦克斯公司就已经未雨绸缪开始研制相关疫苗。在目前有284名志愿者参与的初期研究中,诺瓦瓦克斯公司的研究人员发现新疫苗的有效率达到了81%。研究人员介绍说,这种新疫苗应用的是一种类病毒衣壳技术制备的,对禽流感具有很好的免疫作用。而诺华公司的H7N9疫苗则是通过利用细胞培养技术来研发的,根据其进行的有400名志愿者参与的研究显示,疫苗的有效率达到了85%左右。

  2009年爆发的H1N1疫情波及全球多个国家和地区,给世界各国造成了巨大损失。世界上各大疫苗生产商随后推出的疫苗也未能在疫情再次袭来前起到防护作用,这也遭到了各方广泛诟病。此次,两家疫苗生产巨头开发的疫苗有望在数月后问世。(生物谷Bioon.com)

  详细英文报道:

  Winter's coming, and with it there's a surge of dire warnings that new cases of H7N9 bird flu in China warrant a global pandemic alert. While the most recent pandemic alarms have fizzled out without any major outbreaks of a lethal virus, the federal government has been supporting work on new vaccine technologies. And today two prominent vaccine developers--Novartis ($NVS) and Novavax ($NVAX)--grabbed the R&D spotlight with news that they were able to successfully develop new vaccines within months that could be used against H7N9, demonstrating their broad effectiveness in spurring an immune response in human studies.

  Shares of Novavax popped 9% this morning on the news that its virus-like particle technology platform spawned a vaccine that triggered a significant immune response against H7N9 in 81% of the 284 adults in the study. And the Rockville, MD-based company was able to develop and test the vaccine/adjuvant combo in less than four months after the virus was identified and sequenced.

  "These are very preliminary results, but it appears for the first time that we may have a vaccine that would work against an outbreak" of avian flu, Robin Robinson, director of the Biomedical Advanced Research and Development Authority (BARDA), tells Reuters. "This is a very important milestone. We have a promising vaccine where before we had none."

  Novartis, meanwhile, says it was able to track an 85% response rate among the 400 adults it tested its adjuvanted H7N9 vaccine on. The pharma giant did it using its cell-culture manufacturing technology, which has been developed to rapidly produce mass quantities of vaccines--a vast improvement over the slow egg-based vaccine production system that has been used for generations.

  Novartis and partners at the Craig Venter Institute in San Diego were able to launch a clinical trial in August after the virus was identified in March. The project was funded by BARDA.

  The H1N1 scare back in 2009 spurred a global, multibillion-dollar effort to stockpile vaccines. The campaign highlighted just how long it took to develop and manufacture new vaccines and then spurred a backlash after governments around the globe rushed to buy stockpiles only to see the threat evaporate. In Europe some health officials accused pharma companies of capitalizing on the fear of a lethal pandemic, and memories of the controversy will likely influence any new moves to guard against a new outbreak. This winter's alarm may also fizzle, but these companies have demonstrated that new vaccines can be developed in record time.

  "This rapid response underscores our leadership position in pandemic preparedness," said Andrin Oswald, division head of Novartis Vaccines. "Thanks to our investments into innovative production technologies and adjuvants, we are now able to offer a protective solution for a potentially deadly pandemic virus within a few months after the emergence of the H7N9 virus."

  "The performance of our vaccine candidate is particularly important in light of the speed with which pandemic outbreaks can unfold," says Dr. Lou Fries, Novavax's vice president of clinical and medical affairs. "Often, an initial outbreak of a novel influenza virus is followed by a more severe and widespread outbreak at the onset of the next fall and winter respiratory virus season, as seen in 2009 with H1N1. Unfortunately, vaccine makers in 2009 were unable to produce vaccine in advance of the second wave and there was little impact of vaccine upon H1N1 disease in the first year. Past H7-based vaccine candidates have been poorly immunogenic and thus could not be advanced as viable vaccine candidates. This risk appears to have been overcome by our H7N9 adjuvanted VLP vaccine."

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