CTLA-4-B7 interaction is sufficient to costimulate T cell clonal expansion. - Wikidata - wikimedia - TriplyDB

CTLA-4-B7 interaction is sufficient to costimulate T cell clonal expansion.

CTLA-4-B7 interaction is sufficient to costimulate T cell clonal expansion.

http://www.wikidata.org/entity/Q36377088

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The CD40, CTLA-4, thyroglobulin, TSH receptor, and PTPN22 gene quintet and its contribution to thyroid autoimmunity: back to the future The role of CTLA-4 in the regulation of T cell immune responses.Interaction of CTLA-4 (CD152) with CD80 or CD86 inhibits human T-cell activation.CD80 and CD86 control antiviral CD8+ T-cell function and immune surveillance of murine gammaherpesvirus 68.Pinpointing when T cell costimulatory receptor CTLA-4 must be engaged to dampen diabetogenic T cells Limited density of an antigen presented by RMA-S cells requires B7-1/CD28 signaling to enhance T-cell immunity at the effector phase T regulatory cells: aid or hindrance in the clearance of disease?CTLA-4 blockade decreases TGF-beta, IDO, and viral RNA expression in tissues of SIVmac251-infected macaques.Ligation of cytotoxic T lymphocyte antigen-4 to T cell receptor inhibits T cell activation and directs differentiation into Foxp3+ regulatory T cells Signaling through CD28 and CTLA-4 controls two distinct forms of T cell anergy.Cytotoxic T lymphocyte-associated antigen 4 (CTLA-4) regulates the unfolding of autoimmune diabetes Cytotoxic T lymphocyte antigen 4 (CTLA4) blockade accelerates the acute rejection of cardiac allografts in CD28-deficient mice: CTLA4 can function independently of CD28.Joint genetic susceptibility to type 1 diabetes and autoimmune thyroiditis: from epidemiology to mechanisms.CD28/B7-mediated co-stimulation is critical for early control of murine cytomegalovirus infection B7-CTLA4 interaction enhances both production of antitumor cytotoxic T lymphocytes and resistance to tumor challenge.B7-dependent T-cell costimulation in mice lacking CD28 and CTLA4.Induction of immunologic tolerance for transplantation.Human T-cell clones in long-term culture as a model of immunosenescence.Cytotoxic T lymphocyte antigen 4 (CTLA-4) interferes with extracellular signal-regulated kinase (ERK) and Jun NH2-terminal kinase (JNK) activation, but does not affect phosphorylation of T cell receptor zeta and ZAP70.A reappraisal of CTLA-4 checkpoint blockade in cancer immunotherapy.Analysis of cytotoxic T lymphocyte associated antigen 4 gene polymorphisms in patients with ulcerative colitis

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CTLA-4-B7 interaction is sufficient to costimulate T cell clonal expansion.

http://www.wikidata.org/entity/Q36377088

description

1997 nî lūn-bûn

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1997年の論文

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1997年学术文章

@wuu

1997年学术文章

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1997年学术文章

@zh-hans

1997年学术文章

@zh-my

1997年学术文章

@zh-sg

1997年學術文章

@yue

1997年學術文章

@zh

1997年學術文章

@zh-hant

name

CTLA-4-B7 interaction is sufficient to costimulate T cell clonal expansion.

@ast

CTLA-4-B7 interaction is sufficient to costimulate T cell clonal expansion.

@en

type

label

CTLA-4-B7 interaction is sufficient to costimulate T cell clonal expansion.

@ast

CTLA-4-B7 interaction is sufficient to costimulate T cell clonal expansion.

@en

prefLabel

CTLA-4-B7 interaction is sufficient to costimulate T cell clonal expansion.

@ast

CTLA-4-B7 interaction is sufficient to costimulate T cell clonal expansion.

@en

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P1433

Journal of Experimental Medicine

P1476

CTLA-4-B7 interaction is sufficient to costimulate T cell clonal expansion.

@en

P2093

A Huang

http://www.w3.org/2001/XMLSchema#string

P Zheng

http://www.w3.org/2001/XMLSchema#string

Y Guo

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Y Liu

http://www.w3.org/2001/XMLSchema#string

Y Wu

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P2860

Human T cell activation. II. A new activation pathway used by a major T cell population via a disulfide-bonded dimer of a 44 kilodalton polypeptide (9.3 antigen)

Involvement of T44 molecules in an antigen-independent pathway of T cell activation. Analysis of the correlations to the T cell antigen-receptor complex

T-cell antigen CD28 interacts with the lipid kinase phosphatidylinositol 3-kinase by a cytoplasmic Tyr(P)-Met-Xaa-Met motif

Binding of phosphatidylinositol-3-OH kinase to CD28 is required for T-cell signalling

CTLA-4 binding to the lipid kinase phosphatidylinositol 3-kinase in T cells

CTLA-4 ligation blocks CD28-dependent T cell activation

CD28 and CTLA-4 have opposing effects on the response of T cells to stimulation

Stimulation of CD28 triggers an association between CD28 and phosphatidylinositol 3-kinase in Jurkat T cells

Identification of residues in the V domain of CD80 (B7-1) implicated in functional interactions with CD28 and CTLA4

CD28-mediated signalling co-stimulates murine T cells and prevents induction of anergy in T-cell clones

P304

1327-1335

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scholarly article

P356

10.1084/JEM.185.7.1327

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7

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185

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1997-04-01T00:00:00Z

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9104819

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P932

2196265

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