Skip to main content
. 2014 Sep 12;6(10):1312–1327. doi: 10.15252/emmm.201404114

Figure 7. pDCs and LCs influence disease severity via IL-23.

Figure 7

A Relative Il10 mRNA expression in isolated LCs of indicated mice (n = 7–8).

B PD-L1 expression on epidermal and auricular lymph node LCs (n = 3).

C Relative Il23 mRNA expression in epidermal cells of indicated mice treated as described in Fig 4A (n = 4–6).

D Relative Mx1 mRNA expression (n = 3–7).

E, F Relative Il23 mRNA expression in (E) epidermal (n = 3–7) and (F) dermal cells (n = 3) of indicated mice treated as described in Fig 3A.

G Psoriatic disease was induced by five daily consecutive injections of Tx (▾), and on day 14, when psoriatic disease had developed, mice were treated with an inhibitory anti-IL-23R antibody or an isotype control every other day (▴), and euthanized on day 28.

H Psoriatic inflammation scored at day 14 and day 28 of the indicated mice (n = 9–14).

I Representative images of affected body parts of DKO* mice before and after treatment with anti-IL-23R or isotype control antibody.

J Representative H&E-stained ear sections of indicated mice on day 28. Scale bars represent 100 μm.

K, L Quantification of (K) dermal immune cells (CD45+) (n = 3–4), and (L) dermal monocytes/neutrophils (Gr-1+CD11bhi cells) within CD45+ dermal cells of indicated mice (n = 5–9) measured by flow cytometry.

Data information: Flow cytometric quantification in (K) is depicted as percentage of live cells. Data represent mean ± SEM. Data for (A–F) and (K) were analyzed using unpaired Student's t-test, and for (H) and (L), using Wilcoxon signed-rank test (*< 0.05, **< 0.01) and for (H), additionally using Mann–Whitney U-test (#< 0.05). P-values for this figure are available in Supplementary Table S3.

Source data are available online for this figure.