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Donor regulatory T cells rapidly adapt to recipient tissues to control murine acute graft-versus-host disease

Author

Listed:
  • David J. Dittmar

    (University Hospital Regensburg
    BioNTech SE)

  • Franziska Pielmeier

    (University Hospital Regensburg)

  • Nicholas Strieder

    (Leibniz Institute for Immunotherapy)

  • Alexander Fischer

    (University Hospital Regensburg)

  • Michael Herbst

    (University Hospital Regensburg
    University of Zurich)

  • Hanna Stanewsky

    (University Hospital Regensburg)

  • Niklas Wenzl

    (Leibniz Institute for Immunotherapy)

  • Eveline Röseler

    (Leibniz Institute for Immunotherapy)

  • Rüdiger Eder

    (University Hospital Regensburg)

  • Claudia Gebhard

    (Leibniz Institute for Immunotherapy)

  • Lucia Schwarzfischer-Pfeilschifter

    (University Hospital Regensburg)

  • Christin Albrecht

    (University Hospital Regensburg)

  • Wolfgang Herr

    (University Hospital Regensburg)

  • Matthias Edinger

    (University Hospital Regensburg
    Leibniz Institute for Immunotherapy)

  • Petra Hoffmann

    (University Hospital Regensburg
    Leibniz Institute for Immunotherapy)

  • Michael Rehli

    (University Hospital Regensburg
    Leibniz Institute for Immunotherapy)

Abstract

The adoptive transfer of regulatory T cells is a promising strategy to prevent graft-versus-host disease after allogeneic bone marrow transplantation. Here, we use a major histocompatibility complex-mismatched mouse model to follow the fate of in vitro expanded donor regulatory T cells upon migration to target organs. Employing comprehensive gene expression and repertoire profiling, we show that they retain their suppressive function and plasticity after transfer. Upon entering non-lymphoid tissues, donor regulatory T cells acquire organ-specific gene expression profiles resembling tissue-resident cells and activate hallmark suppressive and cytotoxic pathways, most evidently in the colon, when co-transplanted with graft-versus-host disease-inducing conventional T cells. Dominant T cell receptor clonotypes overlap between organs and across recipients and their relative abundance correlates with protection efficacy. Thus, this study reveals donor regulatory T cell selection and adaptation mechanisms in target organs and highlights protective features of Treg to guide the development of improved graft-versus-host disease prevention strategies.

Suggested Citation

  • David J. Dittmar & Franziska Pielmeier & Nicholas Strieder & Alexander Fischer & Michael Herbst & Hanna Stanewsky & Niklas Wenzl & Eveline Röseler & Rüdiger Eder & Claudia Gebhard & Lucia Schwarzfisch, 2024. "Donor regulatory T cells rapidly adapt to recipient tissues to control murine acute graft-versus-host disease," Nature Communications, Nature, vol. 15(1), pages 1-16, December.
  • Handle: RePEc:nat:natcom:v:15:y:2024:i:1:d:10.1038_s41467-024-47575-z
    DOI: 10.1038/s41467-024-47575-z
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    References listed on IDEAS

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    1. Lei Zhou & Coco Chu & Fei Teng & Nicholas J. Bessman & Jeremy Goc & Endi K. Santosa & Gregory G. Putzel & Hiroki Kabata & Judith R. Kelsen & Robert N. Baldassano & Manish A. Shah & Robbyn E. Sockolow , 2019. "Innate lymphoid cells support regulatory T cells in the intestine through interleukin-2," Nature, Nature, vol. 568(7752), pages 405-409, April.
    2. Clarissa Campbell & Peter T. McKenney & Daniel Konstantinovsky & Olga I. Isaeva & Michail Schizas & Jacob Verter & Cheryl Mai & Wen-Bing Jin & Chun-Jun Guo & Sara Violante & Ruben J. Ramos & Justin R., 2020. "Bacterial metabolism of bile acids promotes generation of peripheral regulatory T cells," Nature, Nature, vol. 581(7809), pages 475-479, May.
    3. Gioele La Manno & Ruslan Soldatov & Amit Zeisel & Emelie Braun & Hannah Hochgerner & Viktor Petukhov & Katja Lidschreiber & Maria E. Kastriti & Peter Lönnerberg & Alessandro Furlan & Jean Fan & Lars E, 2018. "RNA velocity of single cells," Nature, Nature, vol. 560(7719), pages 494-498, August.
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