4.5 Article

Pre-existing influenza-specific nasal IgA or nasal viral infection does not affect live attenuated influenza vaccine immunogenicity in children

Journal

CLINICAL AND EXPERIMENTAL IMMUNOLOGY
Volume 204, Issue 1, Pages 125-133

Publisher

OXFORD UNIV PRESS
DOI: 10.1111/cei.13564

Keywords

IgA; influenza; LAIV; mucosal; schoolchildren

Categories

Funding

  1. NIHR Policy Research Programme (National Vaccine Evaluation Consortium) [039/0031]
  2. National Institute for Health Research (NIHR) Imperial Biomedical Research Centre (BRC)

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This study analyzed the impact of pre-existing influenza-specific nasal immunoglobulin (Ig)A on the immunogenicity of live attenuated influenza vaccine (LAIV) in children aged 6-14 years. The results showed that baseline nasal IgA levels did not affect the IgG response to the vaccine or the detectability of vaccine virus RNA after immunization. Overall, there was no effect of pre-existing influenza-specific nasal antibody on immunogenicity, supporting annual immunization with LAIV in children.
The United Kingdom has a national immunization programme which includes annual influenza vaccination in school-aged children, using live attenuated influenza vaccine (LAIV). LAIV is given annually, and it is unclear whether repeat administration can affect immunogenicity. Because LAIV is delivered intranasally, pre-existing local antibody might be important. In this study, we analysed banked samples from a study performed during the 2017/18 influenza season to investigate the role of pre-existing influenza-specific nasal immunoglobulin (Ig)A in children aged 6-14 years. Nasopharyngeal swabs were collected prior to LAIV immunization to measure pre-existing IgA levels and test for concurrent upper respiratory tract viral infections (URTI). Oral fluid samples were taken at baseline and 21-28 days after LAIV to measure IgG as a surrogate of immunogenicity. Antibody levels at baseline were compared with a pre-existing data set of LAIV shedding from the same individuals, measured by reverse transcription-polymerase chain reaction. There was detectable nasal IgA specific to all four strains in the vaccine at baseline. However, baseline nasal IgA did not correlate with the fold change in IgG response to the vaccine. Baseline nasal IgA also did not have an impact upon whether vaccine virus RNA was detectable after immunization. There was no difference in fold change of antibody between individuals with and without an URTI at the time of immunization. Overall, we observed no effect of pre-existing influenza-specific nasal antibody levels on immunogenicity, supporting annual immunization with LAIV in children.

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