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Blocking the B7-H4 pathway with novel recombinant antibodies enhances T cell-mediated antitumor responses
B7-H4 inhibits T-cell activation and is widely expressed by solid neoplasms. We have recently demonstrated that the expression of B7-H4 on the surface of malignant cells in vivo is inducible, and that novel anti-B7-H4 recombinant antibodies can reverse the inhibition of tumor-specific T cells. Thus,...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Landes Bioscience
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3782523/ https://www.ncbi.nlm.nih.gov/pubmed/24083083 http://dx.doi.org/10.4161/onci.25913 |
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author | Dangaj, Denarda Scholler, Nathalie |
author_facet | Dangaj, Denarda Scholler, Nathalie |
author_sort | Dangaj, Denarda |
collection | PubMed |
description | B7-H4 inhibits T-cell activation and is widely expressed by solid neoplasms. We have recently demonstrated that the expression of B7-H4 on the surface of malignant cells in vivo is inducible, and that novel anti-B7-H4 recombinant antibodies can reverse the inhibition of tumor-specific T cells. Thus, antibodies targeting the B7-H4 pathways may extend the survival of cancer patients by restoring T cell-mediated antitumor responses. |
format | Online Article Text |
id | pubmed-3782523 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Landes Bioscience |
record_format | MEDLINE/PubMed |
spelling | pubmed-37825232013-09-30 Blocking the B7-H4 pathway with novel recombinant antibodies enhances T cell-mediated antitumor responses Dangaj, Denarda Scholler, Nathalie Oncoimmunology Point of View B7-H4 inhibits T-cell activation and is widely expressed by solid neoplasms. We have recently demonstrated that the expression of B7-H4 on the surface of malignant cells in vivo is inducible, and that novel anti-B7-H4 recombinant antibodies can reverse the inhibition of tumor-specific T cells. Thus, antibodies targeting the B7-H4 pathways may extend the survival of cancer patients by restoring T cell-mediated antitumor responses. Landes Bioscience 2013-08-01 2013-07-31 /pmc/articles/PMC3782523/ /pubmed/24083083 http://dx.doi.org/10.4161/onci.25913 Text en Copyright © 2013 Landes Bioscience http://creativecommons.org/licenses/by-nc/3.0/ This is an open-access article licensed under a Creative Commons Attribution-NonCommercial 3.0 Unported License. The article may be redistributed, reproduced, and reused for non-commercial purposes, provided the original source is properly cited. |
spellingShingle | Point of View Dangaj, Denarda Scholler, Nathalie Blocking the B7-H4 pathway with novel recombinant antibodies enhances T cell-mediated antitumor responses |
title | Blocking the B7-H4 pathway with novel recombinant antibodies enhances T cell-mediated antitumor responses |
title_full | Blocking the B7-H4 pathway with novel recombinant antibodies enhances T cell-mediated antitumor responses |
title_fullStr | Blocking the B7-H4 pathway with novel recombinant antibodies enhances T cell-mediated antitumor responses |
title_full_unstemmed | Blocking the B7-H4 pathway with novel recombinant antibodies enhances T cell-mediated antitumor responses |
title_short | Blocking the B7-H4 pathway with novel recombinant antibodies enhances T cell-mediated antitumor responses |
title_sort | blocking the b7-h4 pathway with novel recombinant antibodies enhances t cell-mediated antitumor responses |
topic | Point of View |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3782523/ https://www.ncbi.nlm.nih.gov/pubmed/24083083 http://dx.doi.org/10.4161/onci.25913 |
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