Fig. 3From: A novel “prime and pull” strategy mediated by the combination of two dendritic cell-targeting designs induced protective lung tissue-resident memory T cells against H1N1 influenza virus challengeProduction of effector memory T cells (TEM) before and after intranasal boost immunization in Study 1. At 10 days post-2nd immunization (10 dp2i), spleen samples were collected and subjected to flow cytometry analysis to determine the percentages of CD44+CD62L− TEM cells, CD44+CD62L+ TCM cells and CD44− CD62L+ TNaive cells in the CD3 (A–C), CD4 (D–F) and CD8 (G–I) subgroups. At 10 days post-3rd immunization (10 dp3i), lung samples were collected and subjected to flow cytometry analysis to determine the percentages of TEM, TCM and TNaive cells in the CD4 (J–L) and CD8 (M–O) subgroups (n = 4, *P < 0.05, **P < 0.01, ***P < 0.001, ****P < 0.0001, ns, not significant). Notably, Salmonella strain χ11802 harboring plasmids pYL180 and pYL230 was designated S180 and S230, respectivelyBack to article page