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Extracellular vesicles derived from induced pluripotent stem cells mediate anti-inflammatory effects in primary human macrophages
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  • Published: 09 May 2026

Extracellular vesicles derived from induced pluripotent stem cells mediate anti-inflammatory effects in primary human macrophages

  • Stephen Fitzsimons  ORCID: orcid.org/0000-0002-1576-86321,
  • Silvia Oggero2,
  • Billy P. Egan1,
  • Eugène T. Dillon3,
  • María Muñoz-San Martín4,
  • Shane Clerkin1,
  • Ciarán Kennedy1,
  • Jessica Davis1,
  • Darrell Andrews1,
  • John Crean1 &
  • …
  • Orina Belton1 

Scientific Reports (2026) Cite this article

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Subjects

  • Cell biology
  • Immunology
  • Molecular biology
  • Stem cells

Abstract

Extracellular vesicles derived from induced pluripotent stem cells (iPSC EVs) have immunoregulatory potential with the ability to alter the macrophage phenotype. Modulating the macrophage phenotype towards an anti-inflammatory, pro-resolving state may be beneficial in the treatment of chronic inflammatory diseases. The contents of iPSC EVs and their effects on macrophages are poorly understood. Here iPSC EVs were characterized and analysed by mass spectrometry-based proteomics and a targeted microRNA (miR) panel and their immunomodulatory effects on primary human macrophages were assessed. Podocalyxin-like protein 1 (PODXL1) and Insulin (INS) were the most abundant proteins unique to the iPSC EVs while miR-302d-3p was the most abundant miR. Notably, thioredoxin- and peroxiredoxin-related proteins were detected. iPSC EVs increased the anti-inflammatory associated Mannose Receptor C-Type 1 (MRC1) and miR-21, while monocyte chemoattractant protein 1 (MCP-1) and IL-8 were decreased. Proteomics revealed that treated macrophages had decreased levels of chemoattractant proteins, Azurocidin 1 (AZU1), Growth Differentiation Factor 15 (GDF15), and Ribosomal Protein S19 (RPS19). Conditioned media from macrophages treated with iPSC EVs inhibited monocyte transmigration, a key component in the propagation of inflammation. This study provides insights into the protein and miR cargo of iPSC EVs and highlights their capacity to inhibit chemotactic proteins in macrophages.

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Acknowledgements

We would like to thank UCD Conway Microscopy Core, ONI Nanoimaging Company and the Irish Blood Transfusion Service. We would like to thank Dr Kieran Brennan and Dr Ella Fouhy for supplying reagents which supported this research. We would like to thank Dr Moritz J Strowitzki for his imaging assistance with this research.

Funding

This project was funded by the UCD Strategic Support Wellcome Trust Fund (17533).

Author information

Authors and Affiliations

  1. Diabetes Complications Research Centre, School of Biomolecular and Biomedical Science, Conway Institute, University College Dublin, Belfield, Dublin 4, Ireland

    Stephen Fitzsimons, Billy P. Egan, Shane Clerkin, Ciarán Kennedy, Jessica Davis, Darrell Andrews, John Crean & Orina Belton

  2. William Harvey Research Institute, Barts and the London School of Medicine, Queen Mary University of London, London, UK

    Silvia Oggero

  3. School of Biomolecular and Biomedical Science, Conway Institute, University College Dublin, Belfield, Dublin 4, Ireland

    Eugène T. Dillon

  4. School of Pharmacy and Biomolecular Science, Royal College of Surgeons in Ireland, 123 St Stephen’s Green, Dublin 2, Ireland

    María Muñoz-San Martín

Authors
  1. Stephen Fitzsimons
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  2. Silvia Oggero
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  3. Billy P. Egan
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  4. Eugène T. Dillon
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  7. Ciarán Kennedy
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  10. John Crean
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  11. Orina Belton
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Corresponding authors

Correspondence to Stephen Fitzsimons or Orina Belton.

Ethics declarations

Competing interests

The authors declare no competing interests.

Ethics declaration

Peripheral venous blood was donated by healthy volunteers to the Irish Blood Transfusion Service (IBTS), National Blood Bank located in St. James’s Hospital, James’s Street, Dublin 8 for transfusion and research purposes. Written informed consent was obtained from all volunteers. The IBTS provides de-identified blood components, pro bono, to academic researchers. Written approval was granted by the IBTS to academic researchers at the UCD Conway Institute to utilise these donated blood components (IBTS approval number: 001-03-19). We confirm that all experimental blood processing protocols were approved by the UCD Conway Institute and performed according to Institute guidelines and in compliance with international laws.

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Cite this article

Fitzsimons, S., Oggero, S., Egan, B.P. et al. Extracellular vesicles derived from induced pluripotent stem cells mediate anti-inflammatory effects in primary human macrophages. Sci Rep (2026). https://doi.org/10.1038/s41598-026-49621-w

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  • Received: 22 August 2025

  • Accepted: 15 April 2026

  • Published: 09 May 2026

  • DOI: https://doi.org/10.1038/s41598-026-49621-w

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Keywords

  • Extracellular vesicles
  • iPSCs
  • Macrophages
  • Monocytes
  • Inflammation
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Extracellular vesicles

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