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. 2018 Jan 15;8:1973. doi: 10.3389/fimmu.2017.01973

Figure 2.

Figure 2

Low dose, but not high dose, H56 vaccination post-exposure reduces bacterial loads and lung pathology. (A) lung bacterial loads (log10 CFU) 37 weeks after Mycobacterium tuberculosis challenge from mice vaccinated with the indicated dose of H56 in the post-exposure models. The histopathology data in (B,C) also derives from this experiment (Figure S1B in Supplementary Material, Exp#1). Symbols represent individual mice; lines represent mean ± SEM. (B) representative hematoxylin and eosin (H&E) stains (left panels) and inducible nitric oxide synthase (iNOS) immunohistochemistry (IHC; right panels) of lung tissue from the indicated vaccine groups. Regions of higher magnifications are indicated by inserts (dotted white lines) in lower magnification panels, with magnifications (20×, 100×) indicated above panels. (C) The overall lesion size, number of lesions, and average area affected by tuberculosis inflammation per section are shown. Symbols represent individual mice; lines represent medians. *p < 0.05 by Kruskall–Wallis with Dunn’s posttest for multiple comparisons. (D) extent of lung inflammation 2 weeks after first and 1 week after second and third post-exposure vaccinations (corresponding to 12, 14, and 17 weeks p.i.) as assessed by H&E staining is shown in a separate experiment. Symbols represent mean ± SEM of n = 4–5 mice/group. Differences between vaccine groups were assessed using one-way ANOVA and Tukey’s posttest for multiple comparisons. Statistical significant differences are marked by asterisks, *p < 0.05, **p < 0.01. These experiments were performed once each.