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Mucosal-associated invariant T cells are a profibrogenic immune cell population in the liver

Author

Listed:
  • Pushpa Hegde

    (Centre de Recherche sur l’Inflammation
    Université Paris Diderot)

  • Emmanuel Weiss

    (Centre de Recherche sur l’Inflammation
    Université Paris Diderot
    Assistance Publique-Hôpitaux de Paris)

  • Valérie Paradis

    (Centre de Recherche sur l’Inflammation
    Université Paris Diderot
    Assistance Publique-Hôpitaux de Paris)

  • Jinghong Wan

    (Centre de Recherche sur l’Inflammation
    Université Paris Diderot)

  • Morgane Mabire

    (Centre de Recherche sur l’Inflammation
    Université Paris Diderot)

  • Sukriti Sukriti

    (Centre de Recherche sur l’Inflammation
    Université Paris Diderot)

  • Pierre-Emmanuel Rautou

    (Assistance Publique-Hôpitaux de Paris)

  • Miguel Albuquerque

    (Centre de Recherche sur l’Inflammation
    Université Paris Diderot
    Assistance Publique-Hôpitaux de Paris)

  • Olivia Picq

    (Centre de Recherche sur l’Inflammation
    Université Paris Diderot)

  • Abhishak Chandra Gupta

    (Centre de Recherche sur l’Inflammation
    Université Paris Diderot)

  • Gladys Ferrere

    (Centre de Recherche sur l’Inflammation
    Université Paris Diderot)

  • Hélène Gilgenkrantz

    (Centre de Recherche sur l’Inflammation
    Université Paris Diderot)

  • Badr Kiaf

    (Université Paris-Descartes)

  • Amine Toubal

    (Université Paris-Descartes)

  • Lucie Beaudoin

    (Université Paris-Descartes)

  • Philippe Lettéron

    (Centre de Recherche sur l’Inflammation
    Université Paris Diderot)

  • Richard Moreau

    (Centre de Recherche sur l’Inflammation
    Université Paris Diderot
    Assistance Publique-Hôpitaux de Paris)

  • Agnès Lehuen

    (Université Paris-Descartes)

  • Sophie Lotersztajn

    (Centre de Recherche sur l’Inflammation
    Université Paris Diderot
    Assistance Publique-Hôpitaux de Paris)

Abstract

Liver fibrosis is the common response to chronic liver injury, and leads to cirrhosis and its complications. Persistent inflammation is a driving force of liver fibrosis progression. Mucosal-associated invariant T (MAIT) cells are non-conventional T cells that display altered functions during chronic inflammatory diseases. Here, we show that circulating MAIT cells are reduced in patients with alcoholic or non-alcoholic fatty liver disease-related cirrhosis while they accumulate in liver fibrotic septa. Using two models of chronic liver injury, we demonstrate that MAIT cell-enriched mice show increased liver fibrosis and accumulation of hepatic fibrogenic cells, whereas MAIT cell-deficient mice are resistant. Co-culture experiments indicate that MAIT cells enhance the proinflammatory properties of monocyte-derived macrophages, and promote mitogenic and proinflammatory functions of fibrogenic cells, via distinct mechanisms. Our results highlight the profibrogenic functions of MAIT cells and suggest that targeting MAIT cells may constitute an attractive antifibrogenic strategy during chronic liver injury.

Suggested Citation

  • Pushpa Hegde & Emmanuel Weiss & Valérie Paradis & Jinghong Wan & Morgane Mabire & Sukriti Sukriti & Pierre-Emmanuel Rautou & Miguel Albuquerque & Olivia Picq & Abhishak Chandra Gupta & Gladys Ferrere , 2018. "Mucosal-associated invariant T cells are a profibrogenic immune cell population in the liver," Nature Communications, Nature, vol. 9(1), pages 1-12, December.
  • Handle: RePEc:nat:natcom:v:9:y:2018:i:1:d:10.1038_s41467-018-04450-y
    DOI: 10.1038/s41467-018-04450-y
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    Cited by:

    1. Morgane Mabire & Pushpa Hegde & Adel Hammoutene & Jinghong Wan & Charles Caër & Rola Al Sayegh & Mathilde Cadoux & Manon Allaire & Emmanuel Weiss & Tristan Thibault-Sogorb & Olivier Lantz & Michèle Go, 2023. "MAIT cell inhibition promotes liver fibrosis regression via macrophage phenotype reprogramming," Nature Communications, Nature, vol. 14(1), pages 1-13, December.

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