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. 2024 Mar 8;15:1332588. doi: 10.3389/fimmu.2024.1332588

Figure 3.

Figure 3

Differentiation into MPECs is hindered in a priming environment deficient in GPR41 and GPR43. Ffar2–/–;Ffar3–/– and WT recipients were transferred 5 × 104 naïve WT gBT-I cells and subsequently epicutaneously infected with 1 × 106 PFU HSV-1. (A, B) gBT-I cells were analysed 9 days after infection for SLEC and MPEC proportions in the spleen (A). (B) IFN-γ and TNF-α were measured in gBT-I cells from the spleen following re-stimulation with gB498-505 peptide for 5 hours in the presence of brefeldin A. GzmB and perforin expression was analysed without re-stimulation. (C) Flank skins were harvested 5 days after HSV-1 infection to measure viral titres using PFU assays. Data are presented as representative contour plots or bar graphs with mean + SEM of n = 8 – 10 mice per group from 2 independent experiments. Asterisks indicate statistically significant differences as analysed by Student’s t-tests (non-significant (ns) p ≥ 0.05, **p < 0.01, and ***p < 0.001).