AI Article Synopsis

  • The study examined how prior vaccination affects immune responses in children aged 9-14 receiving the 2010-2011 trivalent inactivated influenza vaccine (TIV).
  • Results showed that children with previous vaccinations had significant T-cell responses and maintained high antibody levels for over seven months, enhancing their protection against both past and future influenza strains.
  • The findings highlight that while influenza viruses mutate and evade immunity, previous exposure to vaccines helps create lasting immune memory that improves responses to new vaccine components.

Article Abstract

Background: Influenza viruses gradually accumulate point mutations, reducing the effectiveness of prior immune protection.

Methods: Children aged 9-14 years received 2010-2011 trivalent inactivated influenza vaccine (TIV). Vaccination history, hemagglutination-inhibition (HI) titers, and cell-mediated immune responses were assessed to investigate the cross-reactivity with past and future influenza virus strains.

Results: 2010-2011 TIV induced significant T-cell responses and HI titers of ≥160, with a fold-rise of ≥4 and titers of ≥100 maintained for >7 months in the majority of children. Pre-existing memory B cells in these children differentiated quickly to antibody-secreting cells to the new vaccine antigens. Children vaccinated in the previous year maintained high HI titers well into 2010, demonstrating elevated HI titers against A/Perth/16/2009, the future (in 2010-2011) H3N2 component. Prior vaccination enhanced CD8 T-cell responses to A/Perth/16/2009. Children vaccinated with the prior 2009-2010 seasonal vaccine also demonstrated higher preexisting levels of interferon γ-secreting CD4CD69 T cells to 2009 pandemic influenza A(H1N1). Children previously vaccinated with 2009-2010 seasonal influenza vaccine also showed greater expansion of tumor necrosis factor α-secreting CD8CD69 T cells to 2009 pandemic influenza A(H1N1) upon vaccination in the 2010-2011 season than those who were not previously vaccinated.

Conclusions: Seasonal influenza viruses continuously drift, which allows them to circumvent protective immunity, but conserved epitopes provide immunological cross-reactivity in children through either vaccination directly or through prime/boost in the prior influenza season.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5731644PMC
http://dx.doi.org/10.1093/infdis/jiw380DOI Listing

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