Figure 1: The lung is a key site of immunity to N. brasiliensis reinfection. | Nature Communications

Figure 1: The lung is a key site of immunity to N. brasiliensis reinfection.

From: ILC2s and T cells cooperate to ensure maintenance of M2 macrophages for lung immunity against hookworms

Figure 1

(a) Mice were primed by s.c. infection and reinfected 30 days later by either s.c. or i.v. inoculation (dark grey). Naïve mice were infected by either s.c.- or i.v. inoculation (light grey). Lung worm burden was assessed 2 days after challenge. The calculated percentage of protection is indicated on the graph (n=5 mice, mean+s.e.m., representative of three independent experiments, ANOVA). (b) Mice were s.c. infected 4, 9, 20 or 30 days before i.v.- or s.c. reinfection. Lung worm burden was assessed 2 days after challenge and protection was calculated as a percentage (n=5 mice, mean+s.e.m., representative of two independent experiments, ANOVA). (c,d) Number of N. brasiliensis larvae in lung tissue (c) and number of red blood cells in the BALF (d) 2, 24 or 48 h post-primary (open boxes) or secondary (closed circles) i.v. infection (with 30 days between primary and reinfection; n=5 mice, mean+s.e.m., representative of two independent experiments, ANOVA). (e) Haematoxylin and eosin staining of lung sections at 48 h post-primary (Nb) or i.v. reinfection (Nb+Nb) infection. Scale bar, 100 μm. (f) Number of N. brasiliensis larvae in the lung parenchyma (light grey bars) or airway space, measured in BALF (dark grey bars), 2, 24 or 48 h post-primary or i.v. reinfection (n=5 mice, mean+s.e.m., representative of two independent experiments, ANOVA). NS, non-significant; P>0.05; P<0.07; *P<0.05; **P<0.01; ***P<0.001; ****P<0.0001.

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