Healthy adult volunteers were 1:1 randomized to receive either intranasal LAIV (2015/2016 Fluenz Tetra or FluMist Tetra, AstraZeneca) or intramuscular quadrivalent inactivated influenza vaccination (Fluarix Tetra, GlaxoSmithKline), as described previously14 . The control group also received a nasal saline spray, while the LAIV group also received an intramuscular saline injection. Three days post-vaccination, all subjects were inoculated with 80,000 colony-forming units (CFU) per nostril of S. pneumoniae 6B type as described previously6 (link),51 . Nasal microbiopsies (ASL Rhino-Pro, Arlington Scientific) and nasal lining fluid samples (Nasosorption, Hunt Developments) were collected and stored at −80 °C as previously described52 (link).