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Highly self-reactive naive CD4 T cells are prone to differentiate into regulatory T cells

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  • Bruno Martin

    (CNRS UMR8104, Cochin Hospital
    INSERM U1016, Cochin Hospital
    Paris Descartes University, Cochin Hospital)

  • Cédric Auffray

    (CNRS UMR8104, Cochin Hospital
    INSERM U1016, Cochin Hospital
    Paris Descartes University, Cochin Hospital)

  • Arnaud Delpoux

    (CNRS UMR8104, Cochin Hospital
    INSERM U1016, Cochin Hospital
    Paris Descartes University, Cochin Hospital)

  • Arnaud Pommier

    (CNRS UMR8104, Cochin Hospital
    INSERM U1016, Cochin Hospital
    Paris Descartes University, Cochin Hospital)

  • Aurélie Durand

    (CNRS UMR8104, Cochin Hospital
    INSERM U1016, Cochin Hospital
    Paris Descartes University, Cochin Hospital)

  • Céline Charvet

    (CNRS UMR8104, Cochin Hospital
    INSERM U1016, Cochin Hospital
    Paris Descartes University, Cochin Hospital)

  • Philippe Yakonowsky

    (CNRS UMR8104, Cochin Hospital
    INSERM U1016, Cochin Hospital
    Paris Descartes University, Cochin Hospital)

  • Hubert de Boysson

    (CNRS UMR8104, Cochin Hospital
    INSERM U1016, Cochin Hospital
    Paris Descartes University, Cochin Hospital)

  • Nelly Bonilla

    (CNRS UMR8104, Cochin Hospital
    INSERM U1016, Cochin Hospital
    Paris Descartes University, Cochin Hospital)

  • Alexandra Audemard

    (CNRS UMR8104, Cochin Hospital
    INSERM U1016, Cochin Hospital
    Paris Descartes University, Cochin Hospital)

  • Tim Sparwasser

    (Institute of Infection Immunology, TWINCORE Center of Experimental and Clinical Infection Research)

  • Benoit L. Salomon

    (CNRS UMR7211, Pitié-Salpêtrière Hospital
    INSERM U959, Pitié-Salpêtrière Hospital
    Paris Sorbonne University, Pitié-Salpêtrière Hospital)

  • Bernard Malissen

    (CNRS UMR6102, Aix-Marseille Université UM 631, 5 Campus de Luminy case 906
    INSERM U631, Aix-Marseille Université UM 631, 5 Campus de Luminy case 906
    Centre d’Immunologie de Marseille-Luminy, Aix-Marseille Université UM 631, 5 Campus de Luminy case 906)

  • Bruno Lucas

    (CNRS UMR8104, Cochin Hospital
    INSERM U1016, Cochin Hospital
    Paris Descartes University, Cochin Hospital)

Abstract

Upon activation, naive CD4 T cells differentiate into a variety of T-helper-cell subsets characterized by different cytokine production and functions. Currently, lineage commitment is considered to depend mostly on the environmental context to which naive CD4 T cells are exposed. Here we challenge this model based on the supposed homogeneity of the naive CD4 T-cell compartment. We show that peripheral naive CD4 T cells can be subdivided into two subsets according to Ly-6C expression. Furthermore, the two newly defined subsets (Ly-6C− and Ly-6C+ naive CD4 T cells) are not equal in their intrinsic ability to commit into the induced regulatory T-cell lineage. Finally, phenotypic analysis, imaging and adoptive transfer experiments reveal that Ly-6C expression is modulated by self-recognition, allowing the dichotomization of the naive CD4 T-cell compartment into two cell subsets with distinct self-reactivity. Altogether, our results show that naive CD4 T cells with the highest avidity for self are prone to differentiate into regulatory T cells.

Suggested Citation

  • Bruno Martin & Cédric Auffray & Arnaud Delpoux & Arnaud Pommier & Aurélie Durand & Céline Charvet & Philippe Yakonowsky & Hubert de Boysson & Nelly Bonilla & Alexandra Audemard & Tim Sparwasser & Beno, 2013. "Highly self-reactive naive CD4 T cells are prone to differentiate into regulatory T cells," Nature Communications, Nature, vol. 4(1), pages 1-12, October.
  • Handle: RePEc:nat:natcom:v:4:y:2013:i:1:d:10.1038_ncomms3209
    DOI: 10.1038/ncomms3209
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    Cited by:

    1. Aurélie Durand & Nelly Bonilla & Théo Level & Zoé Ginestet & Amélie Lombès & Vincent Guichard & Mathieu Germain & Sébastien Jacques & Franck Letourneur & Marcio Cruzeiro & Carmen Marchiol & Gilles Ren, 2024. "Type 1 interferons and Foxo1 down-regulation play a key role in age-related T-cell exhaustion in mice," Nature Communications, Nature, vol. 15(1), pages 1-19, December.

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