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c, WT mice were inoculated with e.c.
Subsequently, mice were inoculated intradermally with B16-F0 tumor cells.
Swiss mice were inoculated intra-peritoneally with viable protoscoleces (PSCs).
Balb/c mice were inoculated with A20HA tumors subcutaneously in one flank.
Sepsis mice were inoculated intraperitoneally with BM-MSCsFluc+/GFP+ (2×106 in 50 ul).
h k, B6 albino mice were inoculated epicutaneously with B16.gB.Luc cells.
Groups of 5 mice were inoculated intragastrically with 0.2 ml of bacteria resuspended in PBS solution.
Immunodeficient NOD.Cg-Prkdcscid Il2rgtm1Wjl/SzJ (NSG) mice were inoculated with 5 × 105 CD19 + Raji cells expressing firefly luciferase.
CD45.2+ wild-type mice were inoculated with E.G7-OVA eight days before the transfer of 1.5 × 105 CD45.1+ OT-I CD8+ iTCM or iTSCM cells.
c, WT mice were inoculated with A20 tumors and tumor were stained for TCs (CD3) and DC (CD11c) after 3 weeks.
The mice were inoculated topically on the wound area (5 µl per wound) with 1.05 × 105 CFU/mouse of strain BAA-1717 suspended in 5 µl PBS.
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