Abstract

The prevalence of antibodies reactive to the 2009 pandemic influenza A(H1N1) was determined in sera collected before the start of the pandemic, during the early phase, and after the main epidemic wave and nationwide vaccination campaign in Norway. A substantial rise in prevalence of antibodies at protective titres, from 3.2% to 44.9%, was observed between August 2009 and January 2010. The highest prevalence, 65.3%, was seen in the age group of 10-19 year-olds.

Highlights

  • A new influenza virus in humans emerged in the spring of 2009 in Mexico

  • This was followed by a comparatively calm period leading up to a major influenza epidemic during October and November 2009, surpassing all previous peaks recorded in the current Norwegian clinical influenza surveillance system which monitors influenza-like illness consultation rates and has been in operation since 1998 [1]

  • The data for the 2008 serum panel show that there was a low frequency of pre-existing protective antibodies to the 2009 pandemic influenza A(H1N1) virus (1.7%, all ages, haemagglutination– inhibition (HI) ≥40)

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Summary

Introduction

A new influenza virus in humans emerged in the spring of 2009 in Mexico. The virus was identified to be a triple reassorted A(H1N1) variant of swine origin but with a still unknown reservoir. A minor epidemic occurred from late July to early August, with a high but gradually declining proportion of travel-related cases This was followed by a comparatively calm period leading up to a major influenza epidemic during October and November 2009, surpassing all previous peaks recorded in the current Norwegian clinical influenza surveillance system which monitors influenza-like illness consultation rates and has been in operation since 1998 [1]. A subset of the serum panel collected in August 2008 (n=689), representative for all age groups and counties across the country, was tested for HI reactivity to the pandemic influenza virus in order to determine the background level of pre-existing antibodies reactive to this virus

Results and discussion
January 2010
Conclusions
Full Text
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