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Unopposed IL-18 signaling leads to severe TLR9-induced macrophage activation syndrome in mice

Charlotte Girard-Guyonvarc'h, Jennifer Palomo, Praxedis Martin, Emiliana Rodriguez, Sabina Troccaz, Gaby Palmer and Cem Gabay

Key points

  • Endogenous IL-18BP is critical to prevent severe macrophage activation syndrome (MAS) upon repetitive TLR9 stimulation.

  • IL-18BP deficiency is associated with elevated plasma levels of free IL-18 and an enhanced IFN-γ molecular signature in TLR9-induced MAS.

Abstract

The term macrophage activation syndrome (MAS) defines a severe, potentially fatal disorder characterized by overwhelming inflammation and multiorgan involvement. Interleukin (IL)-18 is a pro-inflammatory cytokine belonging to the IL-1 family, the activity of which is regulated by its endogenous inhibitor IL-18 binding protein (IL-18BP). Elevated IL-18 levels have been reported in patients with MAS. Herein we show that upon repeated toll-like receptor (TLR)9 stimulation with CpG, IL-18BP-/- mice display severe MAS manifestations, including increased weight loss, splenomegaly, anemia, thrombocytopenia, hyperferritinemia and bone marrow hemophagocytosis as compared to wild-type mice. Serum free IL-18 was detected in CpG-treated IL-18BP-/- mice only. Levels of interferon (IFN)-γ and of IFN-γ signature genes, such as the chemokine Cxcl9 or the transcription factor CIIta were significantly increased in IL-18BP-/- mice. Blocking IL-18R signaling attenuated the severity of MAS and IFN-γ responses in IL-18BP-/- mice. Blocking IFN-γ had comparable effects as IL-18 inhibition on most MAS manifestations. Our data indicate that endogenous IL-18BP exerts a protective role in CpG-induced MAS and that IL-18, which acts upstream of IFN-γ, is involved in the severity of MAS.

  • Submitted June 12, 2017.
  • Accepted December 20, 2017.