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This sequential vaccination regimen consists of one dose of an inactivated monovalent H1N1 influenza vaccine (IIV) followed by one dose of a live attenuated monovalent H1N1 influenza vaccine (LAIV). It was evaluated by the University of Rochester in a Phase 4 clinical trial (NCT01081639) to study the immune response and safety in children aged 4-9 years during the 2009 H1N1 pandemic. The regimen aims to leverage the different immunological pathways of inactivated vaccines, which primarily induce systemic IgG antibodies, and live-attenuated vaccines, which mimic natural infection to stimulate mucosal IgA and cellular immune responses. Both components target the A/California/07/2009 (H1N1) strain.
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See how Gosset can support your research on Influenza A (H1N1) 2009 Monovalent Vaccine + Influenza A (H1N1) Monovalent Vaccine Live-University of Rochester-2009 H1N1 influenza.