Enhanced TCR-induced apoptosis in interferon regulatory factor 4-deficient CD4⁺ Th cells

Abstract

Transcription factors of the interferon regulatory factor (IRF) family contribute to the regulation of cell proliferation and apoptosis. Here, we show that CD4+ T helper (Th) cells lacking IRF4 (IRF4-/-) are highly sensitive to apoptosis. After infection of IRF4-/- mice with the protozoan parasite Leishmania major, the lesion-draining lymph nodes developed the prototypic lymphadenopathy of wild-type mice after 4 wk, but demonstrated almost total loss of cellularity and enhanced apoptosis after 7 wk. In vitro, activation of IRF4-/- CD4+ Th cells led to greatly increased apoptosis compared with wild-type cells. Coculture of IRF4-/- and IRF4+/+ CD4+ cells did not increase survival of IRF4-/- CD4+ cells, indicating that the enhanced rate of IRF4-/- Th cell apoptosis was neither transferable nor due to lack of a cytokine. Enhanced CD4+ cell apoptosis was also observed after anti-CD95 mAb treatment, despite normal CD95 expression. Removal of endogenous cytokines, notably interleukin (IL)-4, led to increased and equally high levels of IRF4-/- and IRF4+/+ cell apoptosis, whereas the protective activity of exogenous IL-4 was reduced in IRF4 -/- CD4+ cells despite normal expression of the IL-4 receptor. Therefore, IRF4 is central in protecting CD4+ cells against proapoptotic stimuli.