Influenza virus vaccines are the main prophylactic strategy
for reducing the burden of influenza morbidity and mortality. Nevertheless the
currently available influenza vaccines induce a narrow and strain specific
immunity and their protective effect is limited by the continuous evolution of
influenza viruses associated with rapidly evolving mutations in key antigenic
sites of the hemagglutinin surface protein.
Besides viral factors, also host and environmental factors
considerably influence the protective effect of influenza vaccines considerably.
Assessment of vaccine effectiveness (VE) using the test-negative
case-control design has revolutionized VE monitoring and has contributed to a
better understanding of suboptimal VE of seasonal influenza vaccines.
This methodology first described for the 2004/05 influenza
season in Canada is now the preferred observational study design to reliably
calculate the effectiveness of seasonal influenza vaccines against medically
attended influenza virus infections.
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