Delaying pyroptosis with an AI-screened gasdermin D pore blocker mitigates inflammatory response

Nat Immunol. 2025 Oct;26(10):1660-1672. doi: 10.1038/s41590-025-02280-x. Epub 2025 Sep 15.

Abstract

The formation of membrane pores by cleaved N-terminal gasdermin D (GSDMD-NT) results in the release of cytokines and inflammatory cell death, known as pyroptosis. Blocking GSDMD-NT pores is an attractive and promising strategy for mitigating inflammation. Here we demonstrate that SK56, an artificial intelligence-screened peptide, effectively obstructs GSDMD-NT pores and inhibits pyroptosis and cytokine release in macrophages and human peripheral blood leukocyte-induced pyroptosis. SK56 prevents septic death induced by lipopolysaccharide or cecal ligation and puncture surgery in mice. SK56 does not influence cleavage of interleukin-1β or GSDMD. Instead, SK56 inhibits the release of cytokines from pyroptotic macrophages, mitigates the activation of primary mouse dendritic cells triggered by incubation with pyroptotic cytomembranes and prevents widespread cell death of human alveolar organoids in an organoid-macrophage coculture model. SK56 blocks GSDMD-NT pores on lipid-bilayer nanoparticles and enters pyroptotic macrophages to inhibit mitochondrial damage. SK56 presents new therapeutic possibilities for counteracting inflammation, which is implicated in numerous diseases.

MeSH terms

  • Animals
  • Artificial Intelligence*
  • Cytokines / metabolism
  • Dendritic Cells / drug effects
  • Dendritic Cells / immunology
  • Disease Models, Animal
  • Gasdermins
  • Humans
  • Inflammation* / drug therapy
  • Inflammation* / immunology
  • Intracellular Signaling Peptides and Proteins* / antagonists & inhibitors
  • Intracellular Signaling Peptides and Proteins* / metabolism
  • Lipopolysaccharides
  • Macrophages / drug effects
  • Macrophages / immunology
  • Macrophages / metabolism
  • Mice
  • Mice, Inbred C57BL
  • Neoplasm Proteins* / antagonists & inhibitors
  • Neoplasm Proteins* / metabolism
  • Phosphate-Binding Proteins* / antagonists & inhibitors
  • Phosphate-Binding Proteins* / metabolism
  • Pyroptosis* / drug effects
  • Pyroptosis* / immunology
  • Sepsis / immunology

Substances

  • Phosphate-Binding Proteins
  • Intracellular Signaling Peptides and Proteins
  • GSDMD protein, human
  • Gsdmd protein, mouse
  • Lipopolysaccharides
  • Neoplasm Proteins
  • Cytokines
  • Gasdermins