Author
Listed:
- 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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