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Cooperative B7-1/2 (CD80/CD86) and B7-DC Costimulation of CD4(+) T Cells Independent of the PD-1 Receptor

B7-DC is a recently discovered member of the B7 family that binds to PD-1 and is selectively expressed by dendritic cells (DCs). It has been shown to either costimulate or inhibit T cell responses. To assess the role of B7-DC in DC–T cell interactions, DCs from B7-DC knockout (KO) mice were generate...

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Autores principales: Shin, Tahiro, Kennedy, Gene, Gorski, Kevin, Tsuchiya, Haruo, Koseki, Haruhiko, Azuma, Miyuki, Yagita, Hideo, Chen, Lieping, Powell, Jonathan, Pardoll, Drew, Housseau, Franck
Formato: Texto
Lenguaje:English
Publicado: The Rockefeller University Press 2003
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2196092/
https://www.ncbi.nlm.nih.gov/pubmed/12847135
http://dx.doi.org/10.1084/jem.20030242
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author Shin, Tahiro
Kennedy, Gene
Gorski, Kevin
Tsuchiya, Haruo
Koseki, Haruhiko
Azuma, Miyuki
Yagita, Hideo
Chen, Lieping
Powell, Jonathan
Pardoll, Drew
Housseau, Franck
author_facet Shin, Tahiro
Kennedy, Gene
Gorski, Kevin
Tsuchiya, Haruo
Koseki, Haruhiko
Azuma, Miyuki
Yagita, Hideo
Chen, Lieping
Powell, Jonathan
Pardoll, Drew
Housseau, Franck
author_sort Shin, Tahiro
collection PubMed
description B7-DC is a recently discovered member of the B7 family that binds to PD-1 and is selectively expressed by dendritic cells (DCs). It has been shown to either costimulate or inhibit T cell responses. To assess the role of B7-DC in DC–T cell interactions, DCs from B7-DC knockout (KO) mice were generated and compared with DCs from wild-type (WT) and B7–1/B7–2 double KO mice. B7–1/B7–2–deficient DCs, while strongly diminished in their ability to stimulate naive CD4(+) T cells, nonetheless retain partial activity. DCs from B7-DC KO mice are diminished in their ability to activate CD4(+) T cells, demonstrating that DC-expressed B7-DC serves a predominantly stimulatory rather than inhibitory function in the initiation of T cell responses. B7-DC costimulates expression of CD40L with faster kinetics than B7–1 and displays potent synergy with B7–1 and B7–2 for T cell proliferation and cytokine production, indicating that these B7 family members work in concert to stimulate T cells. Finally, costimulation with B7-DC alone or in conjunction with B7–1 is PD-1 independent, indicating that B7-DC costimulates T cells via a second receptor.
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spelling pubmed-21960922008-04-11 Cooperative B7-1/2 (CD80/CD86) and B7-DC Costimulation of CD4(+) T Cells Independent of the PD-1 Receptor Shin, Tahiro Kennedy, Gene Gorski, Kevin Tsuchiya, Haruo Koseki, Haruhiko Azuma, Miyuki Yagita, Hideo Chen, Lieping Powell, Jonathan Pardoll, Drew Housseau, Franck J Exp Med Article B7-DC is a recently discovered member of the B7 family that binds to PD-1 and is selectively expressed by dendritic cells (DCs). It has been shown to either costimulate or inhibit T cell responses. To assess the role of B7-DC in DC–T cell interactions, DCs from B7-DC knockout (KO) mice were generated and compared with DCs from wild-type (WT) and B7–1/B7–2 double KO mice. B7–1/B7–2–deficient DCs, while strongly diminished in their ability to stimulate naive CD4(+) T cells, nonetheless retain partial activity. DCs from B7-DC KO mice are diminished in their ability to activate CD4(+) T cells, demonstrating that DC-expressed B7-DC serves a predominantly stimulatory rather than inhibitory function in the initiation of T cell responses. B7-DC costimulates expression of CD40L with faster kinetics than B7–1 and displays potent synergy with B7–1 and B7–2 for T cell proliferation and cytokine production, indicating that these B7 family members work in concert to stimulate T cells. Finally, costimulation with B7-DC alone or in conjunction with B7–1 is PD-1 independent, indicating that B7-DC costimulates T cells via a second receptor. The Rockefeller University Press 2003-07-07 /pmc/articles/PMC2196092/ /pubmed/12847135 http://dx.doi.org/10.1084/jem.20030242 Text en Copyright © 2003, The Rockefeller University Press This article is distributed under the terms of an Attribution–Noncommercial–Share Alike–No Mirror Sites license for the first six months after the publication date (see http://www.rupress.org/terms). After six months it is available under a Creative Commons License (Attribution–Noncommercial–Share Alike 4.0 Unported license, as described at http://creativecommons.org/licenses/by-nc-sa/4.0/).
spellingShingle Article
Shin, Tahiro
Kennedy, Gene
Gorski, Kevin
Tsuchiya, Haruo
Koseki, Haruhiko
Azuma, Miyuki
Yagita, Hideo
Chen, Lieping
Powell, Jonathan
Pardoll, Drew
Housseau, Franck
Cooperative B7-1/2 (CD80/CD86) and B7-DC Costimulation of CD4(+) T Cells Independent of the PD-1 Receptor
title Cooperative B7-1/2 (CD80/CD86) and B7-DC Costimulation of CD4(+) T Cells Independent of the PD-1 Receptor
title_full Cooperative B7-1/2 (CD80/CD86) and B7-DC Costimulation of CD4(+) T Cells Independent of the PD-1 Receptor
title_fullStr Cooperative B7-1/2 (CD80/CD86) and B7-DC Costimulation of CD4(+) T Cells Independent of the PD-1 Receptor
title_full_unstemmed Cooperative B7-1/2 (CD80/CD86) and B7-DC Costimulation of CD4(+) T Cells Independent of the PD-1 Receptor
title_short Cooperative B7-1/2 (CD80/CD86) and B7-DC Costimulation of CD4(+) T Cells Independent of the PD-1 Receptor
title_sort cooperative b7-1/2 (cd80/cd86) and b7-dc costimulation of cd4(+) t cells independent of the pd-1 receptor
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2196092/
https://www.ncbi.nlm.nih.gov/pubmed/12847135
http://dx.doi.org/10.1084/jem.20030242
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