Essential Site Maintenance: Authorea-powered sites will be updated circa 15:00-17:00 Eastern on Tuesday 5 November.
There should be no interruption to normal services, but please contact us at [email protected] in case you face any issues.

loading page

H1N1 G4 swine influenza T cell epitope analysis in swine and human vaccines and circulating strains uncovers potential risk to swine and humans
  • +5
  • Swan Tan,
  • Lenny Moise,
  • Douglas Pearce,
  • Constantinos Kyriakis,
  • Andres GutiĆ©rrez,
  • Ted Ross,
  • Justin Bahl,
  • Anne DeGroot
Swan Tan
University of Georgia College of Veterinary Medicine

Corresponding Author:[email protected]

Author Profile
Lenny Moise
EpiVax Inc
Author Profile
Douglas Pearce
Zoetis Inc
Author Profile
Constantinos Kyriakis
Auburn University College of Veterinary Medicine
Author Profile
Andres GutiƩrrez
EpiVax Inc
Author Profile
Ted Ross
University of Georgia College of Veterinary Medicine
Author Profile
Justin Bahl
University of Georgia
Author Profile
Anne DeGroot
EpiVax Inc
Author Profile

Abstract

Pandemic influenza viruses may emerge from animal reservoirs and spread among humans in the absence of cross-reactive antibodies in the human population. Immune response to highly conserved T cell epitopes in vaccines may still reduce morbidity and limit the spread of the new virus even when cross-protective antibody responses are lacking. We used an established epitope content prediction and comparison tool, EpiCC, to assess the potential for emergent H1N1 G4 swine influenza A virus (G4) to impact swine and human populations. We identified and computed the total cross-conserved T cell epitope content in HA sequences of human seasonal and experimental influenza vaccines, swine influenza vaccines from Europe and the United States (US) against G4. The overall T cell epitope content of US commercial swine vaccines was poorly conserved with G4, with an average T cell epitope coverage of 35.7%. EpiCC scores for the comparison between current human influenza vaccines and circulating human influenza strains were also very low. In contrast, the T cell epitope coverage of a recent European swine influenza vaccine (HL03) was 65.8% against G4. Poor T cell epitope cross-conservation between emergent G4 and swine and human influenza vaccines in the US may enable G4 to spread in swine and spillover to human populations in the absence of protective antibody response. One European influenza vaccine, HL03, may protect against emergent G4. This study illustrates the use of the EpiCC tool for prospective assessment of existing vaccine strains against emergent viruses in swine and human populations.
16 Apr 2022Submitted to Influenza and other respiratory viruses
20 Apr 2022Submission Checks Completed
20 Apr 2022Assigned to Editor
27 Jun 2022Reviewer(s) Assigned
03 Aug 2022Review(s) Completed, Editorial Evaluation Pending
04 Aug 2022Editorial Decision: Revise Minor
29 Aug 20221st Revision Received
05 Sep 2022Submission Checks Completed
05 Sep 2022Assigned to Editor
05 Sep 2022Editorial Decision: Accept
Jan 2023Published in Influenza and Other Respiratory Viruses volume 17 issue 1. 10.1111/irv.13058