4.5 Article

Selection of antigenically advanced variants of seasonal influenza viruses

期刊

NATURE MICROBIOLOGY
卷 1, 期 6, 页码 -

出版社

NATURE PUBLISHING GROUP
DOI: 10.1038/NMICROBIOL.2016.58

关键词

-

资金

  1. Bill & Melinda Gates Foundation Global Health Grant [OPPGH5383]
  2. National Institute of Allergy and Infectious Diseases (NIAID) Public Health Service research grants (USA)
  3. ERATO(Japan Science and Technology Agency)
  4. Center for Research on Influenza Pathogenesis (CRIP) - NIAID [HHSN266200700010C, HHSN272201400008C]
  5. Japan Initiative for Global Research Network on Infectious Diseases
  6. Ministry of Education, Culture, Sports, Science, and Technology, Japan
  7. Ministry of Health, Labour and Welfare, Japan
  8. Strategic Basic Research Program of the Japan Science and Technology Agency
  9. Japan Agency for Medical Research and Development (AMED)
  10. Royal Society
  11. Netherlands Organisation for Scientific Research (NWO) VICI grant
  12. European Union (EU) FP7 programme EMPERIE [223498]
  13. European Union (EU) FP7 programme ANTIGONE [278976]
  14. Human Frontier Science Program (HFSP) programme grant [P0050/2008]
  15. Wellcome [087982AIA]
  16. NIH Director's Pioneer Award [DP1-OD000490-01]
  17. CamGrid, the University of Cambridge distributed computer system
  18. Australian Government Department of Health
  19. MRC [MC_U117512723] Funding Source: UKRI
  20. Medical Research Council [MC_U117512723] Funding Source: researchfish
  21. The Francis Crick Institute [10030] Funding Source: researchfish
  22. Grants-in-Aid for Scientific Research [16K08017] Funding Source: KAKEN

向作者/读者索取更多资源

Influenza viruses mutate frequently, necessitating constant updates of vaccine viruses. To establish experimental approaches that may complement the current vaccine strain selection process, we selected antigenic variants from human H1N1 and H3N2 influenza virus libraries possessing random mutations in the globular head of the haemagglutinin protein ( which includes the antigenic sites) by incubating them with human and/or ferret convalescent sera to human H1N1 and H3N2 viruses. We also selected antigenic escape variants from human viruses treated with convalescent sera and from mice that had been previously immunized against human influenza viruses. Our pilot studies with past influenza viruses identified escape mutants that were antigenically similar to variants that emerged in nature, establishing the feasibility of our approach. Our studies with contemporary human influenza viruses identified escape mutants before they caused an epidemic in 2014-2015. This approach may aid in the prediction of potential antigenic escape variants and the selection of future vaccine candidates before they become widespread in nature.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.5
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据