Uptake of lipids from ascites drives NK cell metabolic dysfunction in ovarian cancer

High-grade serous ovarian cancer (HGSOC) remains an urgent unmet clinical need, with more than 70% of patients presenting with metastatic disease. Many patients develop large volumes of ascites, which promotes metastasis and is associated with poor therapeutic response and survival. Immunotherapy trials have shown limited success, highlighting the need to better understand HGSOC immunology. Here, we analyzed cytotoxic lymphocytes [natural killer (NK), T, and innate T cells] from patients with HGSOC and observed widespread dysfunction across primary and metastatic sites. Although nutrient rich, ascites was immunosuppressive for all lymphocyte subsets. NK cell dysfunction was driven by uptake of polar lipids, with associated dysregulation in lipid storage. Phosphatidylcholine was a key immunosuppressive metabolite, disrupting NK cell membrane order and cytotoxicity. Blocking lipid uptake through SR-B1 protected NK cell antitumor functions in ascites. These findings offer insights into immune suppression in HGSOC and have important implications for the design of future immunotherapies.

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Publication Details

Journal
Science Immunology
Published
2025-05-09
DOI
https://doi.org/10.1126/sciimmunol.adr4795
Citations
15
Primary Topic
Immune Cell Function and Interaction
Type
article
Field-Weighted Citation Impact
11.96
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article

Uptake of lipids from ascites drives NK cell metabolic dysfunction in ovarian cancer

Karen Slattery, Edward Corry, Rafael J. Argüello, Eimear Mylod et al.
15 citations
Science Immunology
Immune Cell Function and Interaction
11.96
article

Uptake of lipids from ascites drives NK cell metabolic dysfunction in ovarian cancer

Karen Slattery, Edward Corry, Rafael J. Argüello, Eimear Mylod, Kate Glennon, Marcia C. Haigis, Donal J. Brennan, Cong-Hui Yao, John Scanlan, Barry Scott, Gavin McManus, Lydia Lynch, Katie O’Brien, Clair M. Gardiner, Orla McGowan, Martin Brennan, Joseph M. Crowley, Ann Treacy
article en
15 citations

Abstract

High-grade serous ovarian cancer (HGSOC) remains an urgent unmet clinical need, with more than 70% of patients presenting with metastatic disease. Many patients develop large volumes of ascites, which promotes metastasis and is associated with poor therapeutic response and survival. Immunotherapy trials have shown limited success, highlighting the need to better understand HGSOC immunology. Here, we analyzed cytotoxic lymphocytes [natural killer (NK), T, and innate T cells] from patients with HGSOC and observed widespread dysfunction across primary and metastatic sites. Although nutrient rich, ascites was immunosuppressive for all lymphocyte subsets. NK cell dysfunction was driven by uptake of polar lipids, with associated dysregulation in lipid storage. Phosphatidylcholine was a key immunosuppressive metabolite, disrupting NK cell membrane order and cytotoxicity. Blocking lipid uptake through SR-B1 protected NK cell antitumor functions in ascites. These findings offer insights into immune suppression in HGSOC and have important implications for the design of future immunotherapies.

Science ImmunologyVol. 10(107)
University College Dublin (IE), Brigham and Women's Hospital (US), Centre National de la Recherche Scientifique (FR), Harvard University (US), Inserm (FR), Princeton University (US), Trinity College Dublin (IE), Mater Misericordiae University Hospital (IE), Boston VA Research Institute (US), Centre d’Immunologie de Marseille-Luminy (FR)
Good health and well-being
Openalex Percentile: Top 1%
Immune Cell Function and Interaction
11.96
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