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. 2021 Mar 9;12:1534. doi: 10.1038/s41467-021-21413-y

Fig. 7. TIGIT+ memory B-cell-modified DCs suppress the induction of IL-21- and IL-4-producing T cell response, while promoting the induction of IL-10-producing CD4+ T cell response.

Fig. 7

ad Representative FACS plots (left panels) and summarized data (right panels) showing the induction of CXCR5+ICOS+ T cell response (a), as well as IL-21- (b), IL-4- (c), and IL-10-expressing (d) CD4+ T cell response elicited by monocyte-derived dendritic cells (MDDCs) modified by TIGIT+ memory B cells. TIGIT+ memory B cells or TIGIT B cells were cocultured with MDDCs for 2 days in the presence of 100 ng/mL LPS before coculturing them for 7 days with FACS-sorted naive CD4+ T cells (CD4+CD45RA+CD45ROCCR7+). PMA, ionomycin, brefeldin A, and monensin cocktails were added 5 h before intracellular staining of indicated cytokines. Isotype antibody staining was performed using mixture of CD4+ T cells cultured in three different conditions. Cells were gated based on isotype antibody staining. Data from four independent experiments performed with cells from different healthy individuals (n = 4). Error bars are mean ± SD. P values were determined with one-way ANOVA with Holm–Sidak’s multiple comparison test (ad).