Fig. 1: Human intestinal CD4+ T cells are phenotypically distinct from their circulating counterparts. | Mucosal Immunology

Fig. 1: Human intestinal CD4+ T cells are phenotypically distinct from their circulating counterparts.

From: CD4+ T cells persist for years in the human small intestine and display a TH1 cytokine profile

Fig. 1

a UMAP visualization after concatenation of flow-cytometric data from PB (red), LP (gray), and IE (green) CD4+ T cells, as described in ref. 8. Representative of three samples. Map of the clusters and representation of each tissue compartment (left). Overlay of the UMAP clusters and the expression levels for each marker, color-coded based on the median fluorescence intensity values (MFI) (right). b Representative contour plots showing L-selectin and CD45RA expression on PB, LP and IE CD4+ T cells and classification of these cells into Tcm, central memory; Tem, effector memory; TemRA, effector memory re-expressing CD45RA; Tn, naïve. c Phenotypic comparison of total PB CD4+ T cells or d effector memory (EM) PB CD4+ T cells with intestinal LP, and IE CD4+ T cells. Compiled data for each marker is given and black bars indicate mean values. One-way ANOVA with Tukey’s multiple comparisons test. ns, not significant; *P ≤ 0.05; **P ≤ 0.01 ***P ≤ 0.001; ****P ≤ 0.0001. e Representative histograms showing the differential phenotypic profile of intestinal CD103 and CD103+ CD4+ T cells from LP and IE for several TRM-related markers. Mean values and SEM is provided. Compiled data of all the experiments are shown in Figure S1C.

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