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  • Poster presentation
  • Open Access

Serological response to pandemic influenza A/H1N1 2009 and seasonal influenza A/H3N2 among health care workers (HCWs) in JIPMER, Puducherry

BMC Infectious Diseases201414 (Suppl 3) :P41

  • Published:


  • Influenza
  • Antibody Titer
  • Influenza Vaccination
  • Seasonal Influenza
  • Pandemic Influenza


Serum antibody titers against influenza viruses are regarded as markers of partial or complete immunoprotection. Antibody titer of ≥40 is associated with at least a 50% reduction in risk for infection or disease.


Serum was collected from 138 HCWs including laboratory personnel, doctors and nurses working at JIPMER, Puducherry during August - October 2013. Details of influenza vaccination and laboratory confirmed influenza infection were noted. Hemagglutination inhibition assay was performed to determine the serum antibody levels against WHO reference antigens – pandemic influenza A (H1N1) A/California/07/2009, seasonal influenza A (H3N2) A/Victoria/361/2011.


Fifty of the HCWs had received pandemic influenza vaccination at least once in the previous three years. All HCWs had antibody titers ≥40 against seasonal influenza A/H3N2. Antibody titers against pandemic influenza A/H1N1 2009 ranged from ≤20 (16.7%) to 320 with 36.9% showing borderline protective titers (=40). Six of the vaccinated HCWs had non-protective antibody titers while 71 unvaccinated HCWs showed protective titers. Only one HCW developed seasonal influenza A/H3N2 infection despite having borderline protective antibody titer of 40 and his convalescent serum sample after two weeks showed fourfold rise in titers.


This study showed protective antibody levels against pandemic influenza A/H1N1 2009 and seasonal influenza A/H3N2 among a large percentage of HCWs, regardless of vaccination status, which may be the primary reason for the low incidence of influenza cases encountered this year.

Authors’ Affiliations

Department of Microbiology, JIPMER, Puducherry, India


© Nandhini and Sujatha; licensee BioMed Central Ltd. 2014

This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. The Creative Commons Public Domain Dedication waiver ( applies to the data made available in this article, unless otherwise stated.