Correction: IRF4 Couples Anabolic Metabolism to Th1 Cell Fate Determination

IRF4 is required for efficient Th1 CD4⁺ effector cell differentiation.

(A) CD4⁺ T cells were labeled with CPD, stimulated with anti-CD3/CD28 + IL-2/IL-12, and restimulated with PMA/ionomycin on day 4, followed by FACS analysis. Representative FACS plots of indicated protein versus CPD (left panels). Quantification of the percent positive population in WT and IRF4-KO CD4⁺ T cells (right panels). (B) Representative FACS plots of TCF1 expression versus CPD after 4 d of activation in Th1-inducing conditions (top left and middle panels). Quantification of TCF1-low population in WT and IRF4-KO CD4⁺ T cells (top right panel). Representative line graphs of T-bet, CD25, and CD62L staining of CD4⁺ T cells (middle row). Quantification of protein expression in WT and IRF4-KO CD4⁺ T cells (bottom row). (C) Increased T-bet protein expression in WT and IRF4-KO CD4⁺ T cells following transduction with T-bet–GFP retrovirus (open graph) compared with untransduced cells (shaded graph) at day 4 postactivation (left panels). Expression of TCF1 (upper right panels) and TNF-α (lower right panels) by CD4⁺ T cells transduced (GFP⁺) or untransduced (GFP⁻) with T-bet–GFP retrovirus, at day 4 postactivation. Plots are representative of three independent experiments. *p < 0.05, **p < 0.01, paired t test.