Making Better Influenza Virus Vaccines?
Open Access
- 1 January 2006
- journal article
- review article
- Published by Centers for Disease Control and Prevention (CDC) in Emerging Infectious Diseases
- Vol. 12 (1) , 61-65
- https://doi.org/10.3201/eid1201.051043
Abstract
Killed and live influenza virus vaccines are effective in preventing and curbing the spread of disease, but new technologies such as reverse genetics could be used to improve them and to shorten the lengthy process of preparing vaccine seed viruses. By taking advantage of these new technologies, we could develop live vaccines that would be safe, cross-protective against variant strains, and require less virus per dose than conventional vaccines. Furthermore, pandemic vaccines against highly virulent strains such as the H5N1 virus can only be generated by reverse genetics techniques. Other technologic breakthroughs should result in effective adjuvants for use with killed and live vaccines, increasing the number of available doses. Finally, universal influenza virus vaccines seem to be within reach. These new strategies will be successful if they are supported by regulatory agencies and if a robust market for influenza virus vaccines against interpandemic and pandemic threats is made and sustained.Keywords
This publication has 34 references indexed in Scilit:
- Chimeric Influenza Virus Hemagglutinin Proteins Containing Large Domains of the Bacillus anthracis Protective Antigen: Protein Characterization, Incorporation into Infectious Influenza Viruses, and AntigenicityJournal of Virology, 2005
- Is this our best shot?Nature, 2005
- It Did Happen Here: Fear And Loathing On The Vaccine TrailHealth Affairs, 2005
- A Noninfectious Simian/Human Immunodeficiency Virus DNA Vaccine That Protects Macaques against AIDSJournal of Virology, 2005
- Immunogenicity and Protection Efficacy of Replication-Deficient Influenza A Viruses with Altered NS1 GenesJournal of Virology, 2004
- Principles Underlying the Development and Use of Live Attenuated Cold-Adapted Influenza A and B Virus VaccinesViral Immunology, 2002
- Immunogenicity and Protective Efficacy of Replication-Incompetent Influenza Virus-Like ParticlesJournal of Virology, 2002
- A DNA transfection system for generation of influenza A virus from eight plasmidsProceedings of the National Academy of Sciences, 2000
- Purified influenza A virus N2 neuraminidase vaccine is immunogenic and non-toxic in humansVaccine, 1995
- Purification of Influenza Virus in the K-II Zonal CentrifugeNature, 1969