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. Author manuscript; available in PMC: 2010 Jun 15.
Published in final edited form as: J Immunol. 2009 Jun 15;182(12):7353–7363. doi: 10.4049/jimmunol.0900657

Figure 7.

Figure 7

Reduced IL-10 expression during secondary flu responses. (A) WT or IL-10 KO mice were infected with 0.1LD50 A/PR8 (H1N1) and on stated days post primary infection, mice were challenged with 300 LD50 A/Philippines (H3N2) and monitored for weight loss (n=5 mice / group). No primed mice succumbed to secondary challenge. (B) After naïve HNT cell transfer, lung and dLN resident donor cells were assayed for IL-10 production by ICCS on stated days post 0.1LD50 A/PR8 challenge. (C) 2×106 naïve or memory HNT cells (Th1-polarized rested effectors) were transferred to naïve hosts subsequently infected with 1 LD50 A/PR8. On stated days, lungs (n=3 / group) were analyzed for IL-10 message. (D) Lung homogenates (n=3 mice / day) from naïve mice infected with 1 LD50 A/PR8 and from mice primed 60 days previously with A/PR8 and challenged with 300 LD50 A/Philippines were analyzed for IL-10 expression. Data in B-D is representative of 2 independent exp.

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