Influenza A H1N1 influenza vaccine safety and immunogenicity of a preliminary study.docVIP

Influenza A H1N1 influenza vaccine safety and immunogenicity of a preliminary study.doc

  1. 1、本文档共16页,可阅读全部内容。
  2. 2、原创力文档(book118)网站文档一经付费(服务费),不意味着购买了该文档的版权,仅供个人/单位学习、研究之用,不得用于商业用途,未经授权,严禁复制、发行、汇编、翻译或者网络传播等,侵权必究。
  3. 3、本站所有内容均由合作方或网友上传,本站不对文档的完整性、权威性及其观点立场正确性做任何保证或承诺!文档内容仅供研究参考,付费前请自行鉴别。如您付费,意味着您自己接受本站规则且自行承担风险,本站不退款、不进行额外附加服务;查看《如何避免下载的几个坑》。如果您已付费下载过本站文档,您可以点击 这里二次下载
  4. 4、如文档侵犯商业秘密、侵犯著作权、侵犯人身权等,请点击“版权申诉”(推荐),也可以打举报电话:400-050-0827(电话支持时间:9:00-18:30)。
  5. 5、该文档为VIP文档,如果想要下载,成为VIP会员后,下载免费。
  6. 6、成为VIP后,下载本文档将扣除1次下载权益。下载后,不支持退款、换文档。如有疑问请联系我们
  7. 7、成为VIP后,您将拥有八大权益,权益包括:VIP文档下载权益、阅读免打扰、文档格式转换、高级专利检索、专属身份标志、高级客服、多端互通、版权登记。
  8. 8、VIP文档为合作方或网友上传,每下载1次, 网站将根据用户上传文档的质量评分、类型等,对文档贡献者给予高额补贴、流量扶持。如果你也想贡献VIP文档。上传文档
查看更多
Influenza A H1N1 influenza vaccine safety and immunogenicity of a preliminary study

 PAGE \* MERGEFORMAT 16 Influenza A H1N1 influenza vaccine safety and immunogenicity of a preliminary study Of: Zhuangmao Xin Fu Cui Yingjie Pan Hongxing Jiang Wei Zhang Xuefeng Wang Meng Yue Zhou Yuchun Hu Xiaokui ZHU Feng Yao was the root of red [Abstract] Objective: To evaluate the cracking of domestic swine influenza virus H1N1 vaccine clinical safety and immunogenicity. Methods: According to randomized, controlled, blind principle, choose the old age (60 years old, Junior (12 to 17 age group and children (3 to 11 years old group of 220 people, according to the proportion of 1 ?U 1 15,30 g influenza H1N1 were inoculated with influenza vaccine, adult (18 to 60 age group of 330 people, according to the proportion of 1 ?U 1 ?U 1 were inoculated 15,30 g Influenza A H1N1 influenza vaccine and placebo controls. Comparison of two doses of vaccine the overall rate of adverse events after immunization, systemic and local adverse reaction rate, HI antibody positive rate, HI antibody (gt; = 1 ?U protection rate of 40 persons, after the HI-free HI antibody after immunization antibody GMT and GMT times higher than the average growth before free. Results: After the free 21 d, each dose group of adverse reactions collected 10.81% of total incidence rate (107/990, are an adverse reaction-based, not observed three or more adverse events. Safety Observation other abnormalities were not observed during the reaction, coupling reaction and the clinical significance of any serious adverse events .30,15 g of HI antibody positive rates were 87.24%, 84.45%, No significant differences were significantly higher than the placebo control group HI antibody positive rate, HI antibody (gt; = 1 ?U 40 for the Protection of 87.94%, respectively, and 85.61%, the difference was not statistically significant, were significantly higher than placebo HI antibody in the control group rate of protection, after-free group was higher than HI antibody GMT 30g 15g group, 15g group than the placebo

文档评论(0)

hhuiws1482 + 关注
实名认证
文档贡献者

该用户很懒,什么也没介绍

版权声明书
用户编号:5024214302000003

1亿VIP精品文档

相关文档