Key result
Pandemic H1N1 vaccination induced significantly higher levels of A/H1N1/California/7/2009-specific antibodies (27.9 vs 20.7 mm2) and long-lived T-cell responses compared to no vaccination.
Why the study?
Does pandemic flu vaccination induce different immune responses compared to natural infection in individuals in Sweden?
Cohort (n=1,971)
Does pandemic flu vaccination induce different immune responses compared to natural infection in individuals in Sweden?
The 2009 pandemic flu vaccine induced qualitatively and quantitatively different, longer-lived cellular immune responses compared to natural infection.
May support stronger, longer-lived responses after vaccination than natural infection; leaves open protection benefits for future pandemic strategies.
BACKGROUND: Previous exposures to flu and subsequent immune responses may impact on 2009/2010 pandemic flu vaccine responses and clinical symptoms upon infection with the 2009 pandemic H1N1 influenza strain. Qualitative and quantitative differences in humoral and cellular immune responses associated with the flu vaccination in 2009/2010 (pandemic H1N1 vaccine) and natural infection have not yet been described in detail. We designed a longitudinal study to examine influenza- (flu-) specific immune responses and the association between pre-existing flu responses, symptoms of influenza-like illness (ILI), impact of pandemic flu infection, and pandemic flu vaccination in a cohort of 2,040 individuals in Sweden in 2009-2010. METHODS: Cellular flu-specific immune responses were assessed by whole-blood antigen stimulation assay, and humoral responses by a single radial hemolysis test. RESULTS: Previous seasonal flu vaccination was associated with significantly lower flu-specific IFN-γ responses (using a whole-blood assay) at study entry. Pandemic flu vaccination induced long-lived T-cell responses (measured by IFN-γ production) to influenza A strains, influenza B strains, and the matrix (M1) antigen. In contrast, individuals with pandemic flu infection (PCR positive) exhibited increased flu-specific T-cell responses shortly after onset of ILI symptoms but the immune response decreased after the flu season (spring 2010). We identified non-pandemic-flu vaccinated participants without ILI symptoms who showed an IFN-γ production profile similar to pandemic-flu infected participants, suggesting exposure without experiencing clinical symptoms. CONCLUSIONS: Strong and long-lived flu-M1 specific immune responses, defined by IFN-γ production, in individuals after vaccination suggest that M1-responses may contribute to protective cellular immune responses. Silent flu infections appeared to be frequent in 2009/2010. The pandemic flu vaccine induced qualitatively and quantitatively different humoral and cellular immune responses as compared to infection with the 2009 H1N1 pandemic H1N1 influenza strain.
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Magalhaes et al. (2014) conducted a cohort in 2009 pandemic H1N1 influenza (n=1,971). Pandemic H1N1 vaccination vs. No pandemic H1N1 vaccination was evaluated on A/H1N1/California/7/2009-specific antibodies (SRH mm2) after the 2009-2010 flu season (p=<0.001). Pandemic H1N1 vaccination induced significantly higher levels of A/H1N1/California/7/2009-specific antibodies (27.9 vs 20.7 mm2) and long-lived T-cell responses compared to no vaccination.
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