Graded Foxo1 activity in Treg cells differentiates tumour immunity from spontaneous autoimmunity
Chong T. Luo,
Will Liao,
Saida Dadi,
Ahmed Toure and
Ming O. Li ()
Additional contact information
Chong T. Luo: Immunology Program, Memorial Sloan Kettering Cancer Center
Will Liao: New York Genome Center
Saida Dadi: Immunology Program, Memorial Sloan Kettering Cancer Center
Ahmed Toure: Immunology Program, Memorial Sloan Kettering Cancer Center
Ming O. Li: Immunology Program, Memorial Sloan Kettering Cancer Center
Nature, 2016, vol. 529, issue 7587, 532-536
Abstract:
The transcription factor Foxo1 is shown to be involved in the determination of distinct subsets of regulatory T (Treg) cells, and the differentiation of activated phenotype Treg cells is associated with the repression of the Foxo1-dependent transcriptional program; constitutively active Foxo1 expression triggers depletion of activated Treg cells in peripheral tissues and leads to CD8 T-cell-mediated autoimmunity and anti-tumour immunity.
Date: 2016
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Persistent link: https://EconPapers.repec.org/RePEc:nat:nature:v:529:y:2016:i:7587:d:10.1038_nature16486
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DOI: 10.1038/nature16486
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