Fig. 3: Increased frequency of CD11c+TbethighCD21low B cells in DS. | Nature

Fig. 3: Increased frequency of CD11c+TbethighCD21low B cells in DS.

From: Autoimmunity in Down’s syndrome via cytokines, CD4 T cells and CD11c+ B cells

Fig. 3

a, Representative t-distributed stochastic neighbour embedding (t-SNE) analysis of a fixed number of B cells to illustrate subset distribution in whole blood from adults with DS and age-matched HC individuals. b,c, The frequency in adults with DS (n = 10) and age-matched HC individuals (n = 10) of total B cells expressed as the percentage of CD66b cells (non-granulocytes) (b) and B cell subsets expressed as the percentage of total B cells (c). dg, The frequency in HC adults (n = 10), adults with DS (n = 10) and patients with SLE (n = 6) of CD11c+ B cells in the IgD+ naive (CD27CD38lowIgD+) or DN (CD27CD38lowIgD) compartments expressed as the percentage of total (d), IgD+ naive (e) or DN (f) B cells, and the log2-transformed ratios of CD11c+ subsets to CD11c subset (rN:aN and DN2:DN1) (g). hk, Intracellular Tbet expression (h), and surface expression of FAS and CD86 (i), CD21 (j) and CXCR5, CCR7, CCR4 and CXCR3 (k) in naive and DN B cells from both HC individuals (n = 2–4) and individuals with DS (n = 3–10). MSI, mean signal intensity; MFI, mean fluorescence intensity. l,m, Correlation of CD11c+ B cells and circulating IL-6 (l) and cTFH1/17 (m). r, Pearson correlation coefficient. In bg, the whiskers denote the minimum and maximum values, the box limits denote quartile 1 to quartile 3, and the centre bar denotes the mean. Significance was assessed using two-tailed unpaired t-tests (b and hk) and one-way ANOVA with Tukey’s post hoc analysis (dg).

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