Trained immunity causes myeloid cell hypercoagulability

The pathogenic basis for increased thrombotic risk in individuals with inflammatory diseases is poorly understood. Myeloid cell "trained immunity" describes persistent innate immune cell memory arising from prior exposure to an inflammatory stimulus, leading to an enhanced immune response to subsequent unrelated stimuli. We identify enhanced myeloid cell prothrombotic activity as a maladaptive consequence of trained immunity. Lipopolysaccharide (LPS) stimulation of macrophages trained previously with β-glucan or heme exhibited significantly enhanced procoagulant activity compared to macrophages stimulated with LPS alone, which was mediated by enhanced acid sphingomyelinase-mediated tissue factor decryption. Furthermore, splenic monocytes isolated from β-glucan-trained mice revealed enhanced procoagulant activity up to 4 weeks after β-glucan administration compared to monocytes from control mice over the same time period. Moreover, hematopoietic progenitor cells and bone marrow interstitial fluid from β-glucan-trained mice had enhanced procoagulant activity compared to control mice. Trained immunity and associated metabolic perturbations may therefore represent an opportunity for targeted intervention in immunothrombotic disease development.

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Publication Details

Journal
Science Advances
Published
2025-03-07
DOI
https://doi.org/10.1126/sciadv.ads0105
Citations
6
Primary Topic
Immune responses and vaccinations
Type
article
Field-Weighted Citation Impact
4.78
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article

Trained immunity causes myeloid cell hypercoagulability

Paula Klavina, Frederick J. Sheedy, James S. O’Donnell, Roger J. S. Preston et al.
6 citations
Science Advances
Immune responses and vaccinations
4.78
article

Trained immunity causes myeloid cell hypercoagulability

Paula Klavina, Frederick J. Sheedy, James S. O’Donnell, Roger J. S. Preston, Seán McCluskey, Tristram A. J. Ryan, Emily A. Day, Aisling M. Rehill, Edmund Gilbert, Hugo Charles‐Messance, Annie M. Curtis, Judith A. Coppinger, Luke O'neill, Gemma León, Jamie M. O’Sullivan, Betül Ünlü, Corrina McMahon, Anna E. Ledwith
article en
6 citations

Abstract

The pathogenic basis for increased thrombotic risk in individuals with inflammatory diseases is poorly understood. Myeloid cell "trained immunity" describes persistent innate immune cell memory arising from prior exposure to an inflammatory stimulus, leading to an enhanced immune response to subsequent unrelated stimuli. We identify enhanced myeloid cell prothrombotic activity as a maladaptive consequence of trained immunity. Lipopolysaccharide (LPS) stimulation of macrophages trained previously with β-glucan or heme exhibited significantly enhanced procoagulant activity compared to macrophages stimulated with LPS alone, which was mediated by enhanced acid sphingomyelinase-mediated tissue factor decryption. Furthermore, splenic monocytes isolated from β-glucan-trained mice revealed enhanced procoagulant activity up to 4 weeks after β-glucan administration compared to monocytes from control mice over the same time period. Moreover, hematopoietic progenitor cells and bone marrow interstitial fluid from β-glucan-trained mice had enhanced procoagulant activity compared to control mice. Trained immunity and associated metabolic perturbations may therefore represent an opportunity for targeted intervention in immunothrombotic disease development.

Science AdvancesVol. 11(10)
Royal College of Surgeons in Ireland (IE), Trinity College Dublin (IE), Children's Health Ireland at Crumlin (IE), National Children’s Research Centre (IE)
Good health and well-being
Openalex Percentile: Top 5%
Immune responses and vaccinations
4.78
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