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Glutathione is critical for NK cell-mediated immunity

  • Luana Guerra
  • , Melanie Grusdat
  • , Takumi Kobayashi
  • , Joseph Longworth
  • , Henry Kurniawan
  • , Davide G. Franchina
  • , Georgios Theodorakis
  • , Carole Binsfeld
  • , Charlène Verschueren
  • , Lynn Bonetti
  • , Anouk Ewen
  • , Leticia Soriano-Baguet
  • , Sarah Alhamouieh
  • , Sophie Farinelle
  • , Catherine Dostert
  • , Ying Chen
  • , Vasilis Vasiliou
  • , Eric Vivier
  • , Philipp A. Lang
  • , Dirk Brenner*
  • *Corresponding author for this work
  • Luxembourg Institute of Health
  • University of Luxembourg
  • Heinrich Heine University Düsseldorf
  • Yale University
  • Centre d'Immunologie de Marseille-Luminy (CIML)
  • Innate Pharma S.A.
  • University Hospital La Timone
  • Paris-Saclay Cancer Cluster
  • Institut Gustave Roussy

Research output: Contribution to journal › Journal article › Research › peer-review

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Abstract

SummaryNatural killer (NK) cells are essential for immune protection against tumors and viruses. Disease environments impose oxidative stress and impair immune cell functions. Glutathione (GSH) is a major cellular antioxidant and is critical for the immune response, but how it modulates NK cell function remains largely unknown. Using a mouse model with a specific deletion of the catalytic subunit of glutamate-cysteine ligase (Gclc) in NK cells, we demonstrate that GSH supports interleukin-15 (IL-15)-driven activation of NK cells. Gclc deficiency causes an intracellular accumulation of reactive oxygen species (ROS), which impairs the metabolism of NK cells. This is accompanied by defective proliferation and cytokine production concurrent with subverted mTOR and STAT5 activation. During acute lymphocytic choriomeningitis virus (LCMV) infection, Gclc-deficient NK cells are unable to suppress the antiviral T cell response. Remarkably, Gclc deficiency impairs NK cell-mediated protection against tumor lung metastases. Our findings highlight an essential role of GSH in maintaining NK cell functionality.

Original languageEnglish
Article number116986
JournalCell Reports
Volume45
Issue number3
ISSN2639-1856
DOIs
Publication statusPublished - 24. Mar 2026

Keywords

  • cancer
  • CP: immunology
  • CP: metabolism
  • cytotoxic T cells
  • glutathione
  • IL-15
  • immunometabolism
  • LCMV
  • metastasis
  • mTOR
  • NK cells
  • redox metabolism

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