Maintenance of the Foxp3-dependent developmental program in mature regulatory T cells requires continued expression of Foxp3. (Q51997055)

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scientific article published on 14 January 2007

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English	Maintenance of the Foxp3-dependent developmental program in mature regulatory T cells requires continued expression of Foxp3.	scientific article published on 14 January 2007

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scholarly article

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Europe PubMed Central

PubMed publication ID

17220892

retrieved

19 April 2018

reference URL

http://europepmc.org/abstract/MED/17220892

title

Maintenance of the Foxp3-dependent developmental program in mature regulatory T cells requires continued expression of Foxp3. (English)

1 reference

stated in

Europe PubMed Central

PubMed publication ID

17220892

retrieved

19 April 2018

reference URL

http://europepmc.org/abstract/MED/17220892

author

Alexander Rudensky

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2

object named as

Alexander Y Rudensky

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Europe PubMed Central

PubMed publication ID

17220892

retrieved

19 April 2018

reference URL

http://europepmc.org/abstract/MED/17220892

author name string

Luke M Williams

series ordinal

1

1 reference

stated in

Europe PubMed Central

PubMed publication ID

17220892

retrieved

19 April 2018

reference URL

http://europepmc.org/abstract/MED/17220892

language of work or name

English

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publication date

14 January 2007

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stated in

Europe PubMed Central

PubMed publication ID

17220892

retrieved

19 April 2018

reference URL

http://europepmc.org/abstract/MED/17220892

published in

Nature Immunology

1 reference

stated in

Europe PubMed Central

PubMed publication ID

17220892

retrieved

19 April 2018

reference URL

http://europepmc.org/abstract/MED/17220892

volume

8

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Europe PubMed Central

PubMed publication ID

17220892

retrieved

19 April 2018

reference URL

http://europepmc.org/abstract/MED/17220892

issue

3

1 reference

stated in

Europe PubMed Central

PubMed publication ID

17220892

retrieved

19 April 2018

reference URL

http://europepmc.org/abstract/MED/17220892

page(s)

277-284

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Europe PubMed Central

PubMed publication ID

17220892

retrieved

19 April 2018

reference URL

http://europepmc.org/abstract/MED/17220892

cites work

Foxp3 programs the development and function of CD4+CD25+ regulatory T cells

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7 January 2021

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Control of regulatory T cell development by the transcription factor Foxp3

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An essential role for Scurfin in CD4+CD25+ T regulatory cells

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Naturally arising Foxp3-expressing CD25+CD4+ regulatory T cells in immunological tolerance to self and non-self

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Regulatory T cell lineage specification by the forkhead transcription factor foxp3

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CD127 expression inversely correlates with FoxP3 and suppressive function of human CD4+ T reg cells

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The amount of scurfin protein determines peripheral T cell number and responsiveness

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Foxp3 interacts with nuclear factor of activated T cells and NF-kappa B to repress cytokine gene expression and effector functions of T helper cells

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Reciprocal developmental pathways for the generation of pathogenic effector TH17 and regulatory T cells

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The orphan nuclear receptor RORgammat directs the differentiation program of proinflammatory IL-17+ T helper cells

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Th17: an effector CD4 T cell lineage with regulatory T cell ties

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Transcription: tantalizing times for T cells

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Conditional deletion of Gata3 shows its essential function in T(H)1-T(H)2 responses.

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GATA-3 deficiency abrogates the development and maintenance of T helper type 2 cells

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Transcriptional activators of helper T cell fate are required for establishment but not maintenance of signature cytokine expression

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Immunologic self-tolerance maintained by CD25(+)CD4(+) regulatory T cells constitutively expressing cytotoxic T lymphocyte-associated antigen 4.

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Engagement of B7 on effector T cells by regulatory T cells prevents autoimmune disease

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Characterization of Foxp3+CD4+CD25+ and IL-10-Secreting CD4+CD25+ T Cells during Cure of Colitis

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Cutting edge: contact-mediated suppression by CD4+CD25+ regulatory cells involves a granzyme B-dependent, perforin-independent mechanism

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Control of experimental inflammatory bowel disease by regulatory T cells

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The evidence for two opposite, ATP-generating and ATP-consuming, extracellular pathways on endothelial and lymphoid cells.

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T regulatory and primed uncommitted CD4 T cells express CD73, which suppresses effector CD4 T cells by converting 5'-adenosine monophosphate to adenosine

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Soluble fibrinogen-like protein 2/fibroleukin exhibits immunosuppressive properties: suppressing T cell proliferation and inhibiting maturation of bone marrow-derived dendritic cells

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An intersection between the self-reactive regulatory and nonregulatory T cell receptor repertoires

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Homeostasis and anergy of CD4(+)CD25(+) suppressor T cells in vivo

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inferred from DOI database lookup

Identifiers

DOI

10.1038/NI1437

1 reference

stated in

Europe PubMed Central

PubMed publication ID

17220892

retrieved

19 April 2018

reference URL

http://europepmc.org/abstract/MED/17220892

PubMed publication ID

17220892

1 reference

stated in

Europe PubMed Central

PubMed publication ID

17220892

retrieved

19 April 2018

reference URL

http://europepmc.org/abstract/MED/17220892

ResearchGate publication ID

6580698

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