Media was replaced every 2 days for a total culture time of 9 days. For CFSE (Molecular Probes, Eugene, OR, USA) labeling, 5 × 107/mL T cells were incubated in prewarmed PBS containing 1 μM CFSE for 10 min at 37°C followed by extensive washing and resuspension in PBS for adoptive transfer. Mixed BM chimeras in which only the αβ T cells lack 4–1BB were generated using TCRα−/− and 4–1BB−/− mice as described previously [49]. For the generation of the 4–1BBL−/− BM chimeras, 5 × 106 congenically marked 4–1BBL−/− or WT BM cells were used to reconstitute lethally irradiated WT or 4–1BBL−/− mice. All irradiated BM reconstituted mice were given water supplemented with 2 mg/mL of neomycin

sulfate (Bio-Shop, Burlington, Ontario,

Canada) during the first 4 weeks, and they were further rested for an additional 2 months before use. Three million OT-I T cells, prepared as above, were delivered i.v. to the mice and their recovery Selumetinib datasheet from spleen, LN, and BM analyzed 30 days later. Influenza A/PR8 and A/HKx31 viruses were grown in eggs and their tissue culture infectious dose determined by infection of MDCK cells [50]. Age- and sex-matched mice were used for infection. A dose of 100 HAU influenza A/X31 in 200 μL volume was used for primary intraperitoneal infection. Influenza A/X31 primed mice were rested for at least 30 days before challenge with influenza A/PR8 at a dose of 100 HAU in 200 μL intraperitoneally. Analysis of influenza NP366–374-specific CD8+ T cells using MHC tetramers as well as CD107a and intracellular cytokine staining Alpelisib research buy following a 6-hour restimulation was carried out as previously described [28]. H-2Db/NP366–374

tetramers were provided by the National Institute for Allergy and Infectious Diseases tetramer facility (Emory University, Atlanta, GA, USA). Uninfected mice were used as negative controls for Db/NP366–374 tetramer staining. Isotype or fluorescence minus one controls were used as negative controls for cytokine staining. Congenically marked OT-I TCR transgenic cells were tracked using PE- or allophycocyanin-anti-mouse CD45.2 (eBioscience), Pacific Blue-anti-CD45.1 (Biolegend), FITC-anti-Vβ5.1 (BD Biosciences), biotin-anti-Vα2 and PerCP-anti-mouse CD8+ (BD Biosciences). Other antibodies used in this study included Cediranib (AZD2171) allophycocyanin-anti-mouse IFN-γ, FITC-anti-CD107a, PE- or PE-Cy5- or allophycocyanin-anti-CD44, FITC-anti-Ter119, Pe-Cy7- or PE-anti-mouse CD3, biotinylated-anti-mouse-4–1BB (clone 3H3), Alexa Fluor450- or PE-anti-B220, PE-, PE-Cy7- or allophycocyanin-anti-CD11c, Alexa Fluor488 anti-Gr1, PE-anti-Ly-6C, PE-anti-MHC-II, PE-Cy7-anti-F4/80, PerCP- or PE-Cy7-anti-CD11b, PE-Cy5.5-anti-mouse TCRβ, PE-Cy5.5-anti-mouse CD19, and FITC-anti-PDCA-1. The 4–1BB-deficient mouse was used as a negative control for analysis of 4–1BB expression on CD8+ T cells. Detection of 4–1BBL was done by i.v.