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Identification of a human OX-40 ligand, a costimulator of CD4+ T cells with homology to tumor necrosis factor
The human OX-40 cell surface antigen is a CD4+ T cell activation marker that acts as a costimulatory receptor and is a member of the nerve growth factor receptor/tumor necrosis factor (TNF) receptor family. Using a soluble form of the receptor, the extracellular region fused with human immunoglobuli...
Formato: | Texto |
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Lenguaje: | English |
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The Rockefeller University Press
1994
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2191595/ https://www.ncbi.nlm.nih.gov/pubmed/7913952 |
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collection | PubMed |
description | The human OX-40 cell surface antigen is a CD4+ T cell activation marker that acts as a costimulatory receptor and is a member of the nerve growth factor receptor/tumor necrosis factor (TNF) receptor family. Using a soluble form of the receptor, the extracellular region fused with human immunoglobulin Fc, we expression cloned the human OX-40 ligand cDNA from a library derived from an activated B lymphoblastoid cell line MSAB. The encoded protein is identified as gp34, a type II transmembrane antigen previously known to be expressed only by human T cell lymphotropic virus 1-infected cells. We describe gp34 as a new member of the TNF family, and find that the recombinant ligand expressed in COS cells costimulates phorbol myristate acetate, phytohemagglutinin, and anti-CD3-induced CD4+ T cell proliferation. |
format | Text |
id | pubmed-2191595 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 1994 |
publisher | The Rockefeller University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-21915952008-04-16 Identification of a human OX-40 ligand, a costimulator of CD4+ T cells with homology to tumor necrosis factor J Exp Med Articles The human OX-40 cell surface antigen is a CD4+ T cell activation marker that acts as a costimulatory receptor and is a member of the nerve growth factor receptor/tumor necrosis factor (TNF) receptor family. Using a soluble form of the receptor, the extracellular region fused with human immunoglobulin Fc, we expression cloned the human OX-40 ligand cDNA from a library derived from an activated B lymphoblastoid cell line MSAB. The encoded protein is identified as gp34, a type II transmembrane antigen previously known to be expressed only by human T cell lymphotropic virus 1-infected cells. We describe gp34 as a new member of the TNF family, and find that the recombinant ligand expressed in COS cells costimulates phorbol myristate acetate, phytohemagglutinin, and anti-CD3-induced CD4+ T cell proliferation. The Rockefeller University Press 1994-08-01 /pmc/articles/PMC2191595/ /pubmed/7913952 Text en 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 | Articles Identification of a human OX-40 ligand, a costimulator of CD4+ T cells with homology to tumor necrosis factor |
title | Identification of a human OX-40 ligand, a costimulator of CD4+ T cells with homology to tumor necrosis factor |
title_full | Identification of a human OX-40 ligand, a costimulator of CD4+ T cells with homology to tumor necrosis factor |
title_fullStr | Identification of a human OX-40 ligand, a costimulator of CD4+ T cells with homology to tumor necrosis factor |
title_full_unstemmed | Identification of a human OX-40 ligand, a costimulator of CD4+ T cells with homology to tumor necrosis factor |
title_short | Identification of a human OX-40 ligand, a costimulator of CD4+ T cells with homology to tumor necrosis factor |
title_sort | identification of a human ox-40 ligand, a costimulator of cd4+ t cells with homology to tumor necrosis factor |
topic | Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2191595/ https://www.ncbi.nlm.nih.gov/pubmed/7913952 |