Journal article
Protection of mice against lethal challenge with 2009 H1N1 influenza A virus by 1918-like and classical swine H1N1 based vaccines
PLoS pathogens, Vol.6(1), pp.e1000745-e1000745
01/29/2010
DOI: 10.1371/journal.ppat.1000745
PMCID: PMC2813279
PMID: 20126449
Abstract
The recent 2009 pandemic H1N1 virus infection in humans has resulted in nearly 5,000 deaths worldwide. Early epidemiological findings indicated a low level of infection in the older population (>65 years) with the pandemic virus, and a greater susceptibility in people younger than 35 years of age, a phenomenon correlated with the presence of cross-reactive immunity in the older population. It is unclear what virus(es) might be responsible for this apparent cross-protection against the 2009 pandemic H1N1 virus. We describe a mouse lethal challenge model for the 2009 pandemic H1N1 strain, used together with a panel of inactivated H1N1 virus vaccines and hemagglutinin (HA) monoclonal antibodies to dissect the possible humoral antigenic determinants of pre-existing immunity against this virus in the human population. By hemagglutinination inhibition (HI) assays and vaccination/challenge studies, we demonstrate that the 2009 pandemic H1N1 virus is antigenically similar to human H1N1 viruses that circulated from 1918-1943 and to classical swine H1N1 viruses. Antibodies elicited against 1918-like or classical swine H1N1 vaccines completely protect C57B/6 mice from lethal challenge with the influenza A/Netherlands/602/2009 virus isolate. In contrast, contemporary H1N1 vaccines afforded only partial protection. Passive immunization with cross-reactive monoclonal antibodies (mAbs) raised against either 1918 or A/California/04/2009 HA proteins offered full protection from death. Analysis of mAb antibody escape mutants, generated by selection of 2009 H1N1 virus with these mAbs, indicate that antigenic site Sa is one of the conserved cross-protective epitopes. Our findings in mice agree with serological data showing high prevalence of 2009 H1N1 cross-reactive antibodies only in the older population, indicating that prior infection with 1918-like viruses or vaccination against the 1976 swine H1N1 virus in the USA are likely to provide protection against the 2009 pandemic H1N1 virus. This data provides a mechanistic basis for the protection seen in the older population, and emphasizes a rationale for including vaccination of the younger, naïve population. Our results also support the notion that pigs can act as an animal reservoir where influenza virus HAs become antigenically frozen for long periods of time, facilitating the generation of human pandemic viruses.
Details
- Title: Subtitle
- Protection of mice against lethal challenge with 2009 H1N1 influenza A virus by 1918-like and classical swine H1N1 based vaccines
- Creators
- Balaji Manicassamy - Department of Microbiology, Mount Sinai School of Medicine, New York, New York, United States of AmericaRafael A MedinaRong HaiTshidi TsibaneSilke StertzEstanislao Nistal-VillánPeter PaleseChristopher F BaslerAdolfo García-Sastre
- Resource Type
- Journal article
- Publication Details
- PLoS pathogens, Vol.6(1), pp.e1000745-e1000745
- DOI
- 10.1371/journal.ppat.1000745
- PMID
- 20126449
- PMCID
- PMC2813279
- NLM abbreviation
- PLoS Pathog
- ISSN
- 1553-7366
- eISSN
- 1553-7374
- Publisher
- Public Library of Science
- Grant note
- 3 U19 AI062623-05S1 / NIAID NIH HHS P01 AI058113 / NIAID NIH HHS HHSN266200700010C / PHS HHS AI058113 / NIAID NIH HHS U19 AI062623 / NIAID NIH HHS HHSN266200700010C / NIAID NIH HHS
- Language
- English
- Date published
- 01/29/2010
- Academic Unit
- Microbiology and Immunology
- Record Identifier
- 9984083271002771
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