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. Author manuscript; available in PMC: 2023 Feb 8.
Published in final edited form as: Immunity. 2022 Feb 8;55(2):254–271.e7. doi: 10.1016/j.immuni.2021.12.014

Figure 1: IL-5+ type 2 lymphocytes expand in lung and liver parenchyma during type 2 inflammation.

Figure 1:

(A) Schematics of lung topography highlighting adventitial (pink) and parenchymal (teal) domains.

(B-D) Confocal imaging of lung thick-sections (left) or surface-rendered three-dimensional reconstruction (right) from IL-5+ T2L lineage tracker naïve mice, Nippostrongylus brasiliensis infected (Nb) at day 30 (D30) post-infection (PI), or IL-33 treated at D30 post treatment, as indicated. 3 independent experiments, total N=5–6 mice/group.

(E-F, H-I) Quantitative analysis of lung and liver thick-section confocal images as percent parenchymal IL-5+ T2Ls of total IL-5+ T2Ls (E and H) or parenchymal IL-5+ T2L numbers per tissue volume (F and I). Pooled from 3 independent experiments, total N=5–6 mice/group.

(G) Confocal imaging of liver thick-sections at resting, D30 PI with Nb and D30 post IL-33 treatment showing surface-rendered reconstruction, as described in B-D.

(J-L) Confocal imaging of lung and liver sections at indicated days post IL-33 treatment showing surface-rendered 3D reconstruction, as described in B-D and quantitative imaging analysis (K-L) of parenchymal IL-5+ T2L accumulation as a percent of total IL-5+ T2L. Images and quantification from 2 independent experiments, total N=4–5 mice per time point.

See also Figure S1.