Influenza vaccine immunology
- PMID: 21198671
- DOI: 10.1111/j.1600-065X.2010.00974.x
Influenza vaccine immunology
Abstract
Studying the spread of influenza in human populations and protection by influenza vaccines provides important insights into immunity against influenza. The 2009 H1N1 pandemic has taught the most recent lessons. Neutralizing and receptor-blocking antibodies against hemagglutinin are the primary means of protection from the spread of pandemic and seasonal strains. Anti-neuraminidase antibodies seem to play a secondary role. More broadly cross-reactive forms of immunity may lessen disease severity but are insufficient to prevent epidemic spread. Priming by prior exposure to related influenza strains through infection or immunization permits rapid, potent antibody responses to immunization. Priming is of greater importance to the design of immunization strategies than the immunologically fascinating phenomenon of dominant recall responses to previously encountered strains (original antigenic sin). Comparisons between non-adjuvanted inactivated vaccines and live attenuated vaccines demonstrate that both can protect, with some advantage of live attenuated vaccines in children and some advantage of inactivated vaccines in those with multiple prior exposures to influenza antigens. The addition of oil-in-water emulsion adjuvants to inactivated vaccines provides enhanced functional antibody titers, greater breadth of antibody cross-reactivity, and antigen dose sparing. The MF59 adjuvant broadens the distribution of B-cell epitopes recognized on HA and NA following immunization.
© 2010 John Wiley & Sons A/S.
Similar articles
-
Immunization against influenza A virus: comparison of conventional inactivated, live-attenuated and recombinant baculovirus produced purified hemagglutinin and neuraminidase vaccines in a murine model system.Virology. 2005 Sep 1;339(2):273-80. doi: 10.1016/j.virol.2005.06.006. Virology. 2005. PMID: 15996702
-
Vaccines with MF59 adjuvant expand the antibody repertoire to _target protective sites of pandemic avian H5N1 influenza virus.Sci Transl Med. 2010 Jan 20;2(15):15ra5. doi: 10.1126/scitranslmed.3000624. Sci Transl Med. 2010. PMID: 20371470
-
Enhanced immunogenicity of seasonal influenza vaccines in young children using MF59 adjuvant.Pediatr Infect Dis J. 2009 Jul;28(7):563-71. doi: 10.1097/INF.0b013e31819d6394. Pediatr Infect Dis J. 2009. PMID: 19561422 Clinical Trial.
-
Trends in development of the influenza vaccine with broader cross-protection.Acta Virol. 2010;54(1):7-19. Acta Virol. 2010. PMID: 20201609 Review.
-
[Immunity against influenza virus infection].Nihon Rinsho. 2010 Sep;68(9):1625-30. Nihon Rinsho. 2010. PMID: 20845738 Review. Japanese.
Cited by
-
Long-term immunogenicity of the pandemic influenza A/H1N1 2009 vaccine among health care workers: influence of prior seasonal influenza vaccination.Clin Vaccine Immunol. 2013 Apr;20(4):513-6. doi: 10.1128/CVI.00725-12. Epub 2013 Jan 30. Clin Vaccine Immunol. 2013. PMID: 23365206 Free PMC article.
-
Inferring reasons for the failure of Staphylococcus aureus vaccines in clinical trials.Front Cell Infect Microbiol. 2012 Feb 22;2:16. doi: 10.3389/fcimb.2012.00016. eCollection 2012. Front Cell Infect Microbiol. 2012. PMID: 22919608 Free PMC article. Review. No abstract available.
-
Selection of therapeutic H5N1 monoclonal antibodies following IgVH repertoire analysis in mice.Antiviral Res. 2016 Jul;131:100-8. doi: 10.1016/j.antiviral.2016.04.001. Epub 2016 Apr 21. Antiviral Res. 2016. PMID: 27109194 Free PMC article.
-
Memory CD4+ T cells enhance B-cell responses to drifting influenza immunization.Eur J Immunol. 2019 Feb;49(2):266-276. doi: 10.1002/eji.201847852. Epub 2018 Dec 21. Eur J Immunol. 2019. PMID: 30548475 Free PMC article.
-
The Role of Pre-existing Cross-Reactive Central Memory CD4 T-Cells in Vaccination With Previously Unseen Influenza Strains.Front Immunol. 2019 Apr 4;10:593. doi: 10.3389/fimmu.2019.00593. eCollection 2019. Front Immunol. 2019. PMID: 31019503 Free PMC article.
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Other Literature Sources
Medical