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TIV + LAIV refers to a vaccination regimen involving the sequential or comparative administration of the Trivalent Inactivated Influenza Vaccine (TIV) and the Live Attenuated Influenza Vaccine (LAIV). This specific combination was the subject of a Phase 4 clinical trial (NCT01184690) sponsored by the University of Rochester to evaluate the safety, viral shedding, and immunogenicity in healthy children aged 2 to 9 years. The TIV component is an inactivated vaccine typically administered via intramuscular injection, while the LAIV component (such as FluMist) contains live-attenuated viruses administered intranasally. The vaccines used in the Rochester study targeted three influenza strains: A/California/7/2009 (H1N1), A/Perth/16/2009 (H3N2), and B/Brisbane/60/2008 (Victoria lineage), which were the recommended components for the 2010–2011 Northern Hemisphere influenza season.
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