| Literature DB >> 33922875 |
Esther Dawen Yu1, Alba Grifoni1, Aaron Sutherland1, Hannah Voic1, Eric Wang1, April Frazier1, Natalia Jimenez-Truque2, Sandra Yoder2, Sabrina Welsh3, Stacey Wooden4, Wayne Koff3, Buddy Creech2, Alessandro Sette1,5, Ricardo da Silva Antunes1.
Abstract
The role of T cell immunity has been acknowledged in recent vaccine development and evaluation. We tested the humoral and cellular immune responses to Flucelvax®, a quadrivalent inactivated seasonal influenza vaccine containing two influenza A (H1N1 Singapore/GP1908/2015 IVR-180 and H3N2 North Carolina/04/2016) and two influenza B (Iowa/06/2017 and Singapore/INFTT-16-0610/2016) virus strains, using peripheral blood mononuclear cells stimulated by pools of peptides overlapping all the individual influenza viral protein components. Baseline reactivity was detected against all four strains both at the level of CD4 and CD8 responses and targeting different proteins. CD4 T cell reactivity was mostly directed to HA/NA proteins in influenza B strains, and NP/M1/M2/NS1/NEP proteins in the case of the Influenza A strains. CD8 responses to both influenza A and B viruses preferentially targeted the more conserved core viral proteins. Following vaccination, both CD4 and CD8 responses against the various influenza antigens were increased in day 15 to day 91 post vaccination period, and maintained a Th1 polarized profile. Importantly, no vaccine interference was detected, with the increased responses balanced across all four included viral strains for both CD4 and CD8 T cells, and targeting HA and multiple additional viral antigens.Entities:
Keywords: T cells; cytokine polarization; influenza viruses; protein immunodominance; vaccine
Year: 2021 PMID: 33922875 DOI: 10.3390/vaccines9050426
Source DB: PubMed Journal: Vaccines (Basel) ISSN: 2076-393X