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Induction of Tumor-specific T Cell Immunity by Anti-DR5 Antibody Therapy
Because tumor necrosis factor–related apoptosis-inducing ligand (TRAIL) preferentially induces apoptosis in tumor cells and plays a critical role in tumor surveillance, its receptor is an attractive target for antibody-mediated tumor therapy. Here we report that a monoclonal antibody (mAb) against t...
Autores principales: | , , , , , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
Publicado: |
The Rockefeller University Press
2004
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2211825/ https://www.ncbi.nlm.nih.gov/pubmed/14769851 http://dx.doi.org/10.1084/jem.20031457 |
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author | Takeda, Kazuyoshi Yamaguchi, Noriko Akiba, Hisaya Kojima, Yuko Hayakawa, Yoshihiro Tanner, Jane E. Sayers, Thomas J. Seki, Naoko Okumura, Ko Yagita, Hideo Smyth, Mark J. |
author_facet | Takeda, Kazuyoshi Yamaguchi, Noriko Akiba, Hisaya Kojima, Yuko Hayakawa, Yoshihiro Tanner, Jane E. Sayers, Thomas J. Seki, Naoko Okumura, Ko Yagita, Hideo Smyth, Mark J. |
author_sort | Takeda, Kazuyoshi |
collection | PubMed |
description | Because tumor necrosis factor–related apoptosis-inducing ligand (TRAIL) preferentially induces apoptosis in tumor cells and plays a critical role in tumor surveillance, its receptor is an attractive target for antibody-mediated tumor therapy. Here we report that a monoclonal antibody (mAb) against the mouse TRAIL receptor, DR5, exhibited potent antitumor effects against TRAIL-sensitive tumor cells in vivo by recruiting Fc receptor–expressing innate immune cells, with no apparent systemic toxicity. Administration of the agonistic anti-DR5 mAb also significantly inhibited experimental and spontaneous tumor metastases. Notably, the anti-DR5 mAb-mediated tumor rejection by innate immune cells efficiently evoked tumor-specific T cell immunity that could also eradicate TRAIL-resistant variants. These results suggested that the antibody-based therapy targeting DR5 is an efficient strategy not only to eliminate TRAIL-sensitive tumor cells, but also to induce tumor-specific T cell memory that affords a long-term protection from tumor recurrence. |
format | Text |
id | pubmed-2211825 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2004 |
publisher | The Rockefeller University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-22118252008-03-11 Induction of Tumor-specific T Cell Immunity by Anti-DR5 Antibody Therapy Takeda, Kazuyoshi Yamaguchi, Noriko Akiba, Hisaya Kojima, Yuko Hayakawa, Yoshihiro Tanner, Jane E. Sayers, Thomas J. Seki, Naoko Okumura, Ko Yagita, Hideo Smyth, Mark J. J Exp Med Article Because tumor necrosis factor–related apoptosis-inducing ligand (TRAIL) preferentially induces apoptosis in tumor cells and plays a critical role in tumor surveillance, its receptor is an attractive target for antibody-mediated tumor therapy. Here we report that a monoclonal antibody (mAb) against the mouse TRAIL receptor, DR5, exhibited potent antitumor effects against TRAIL-sensitive tumor cells in vivo by recruiting Fc receptor–expressing innate immune cells, with no apparent systemic toxicity. Administration of the agonistic anti-DR5 mAb also significantly inhibited experimental and spontaneous tumor metastases. Notably, the anti-DR5 mAb-mediated tumor rejection by innate immune cells efficiently evoked tumor-specific T cell immunity that could also eradicate TRAIL-resistant variants. These results suggested that the antibody-based therapy targeting DR5 is an efficient strategy not only to eliminate TRAIL-sensitive tumor cells, but also to induce tumor-specific T cell memory that affords a long-term protection from tumor recurrence. The Rockefeller University Press 2004-02-16 /pmc/articles/PMC2211825/ /pubmed/14769851 http://dx.doi.org/10.1084/jem.20031457 Text en Copyright © 2004, 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 Takeda, Kazuyoshi Yamaguchi, Noriko Akiba, Hisaya Kojima, Yuko Hayakawa, Yoshihiro Tanner, Jane E. Sayers, Thomas J. Seki, Naoko Okumura, Ko Yagita, Hideo Smyth, Mark J. Induction of Tumor-specific T Cell Immunity by Anti-DR5 Antibody Therapy |
title | Induction of Tumor-specific T Cell Immunity by Anti-DR5 Antibody Therapy |
title_full | Induction of Tumor-specific T Cell Immunity by Anti-DR5 Antibody Therapy |
title_fullStr | Induction of Tumor-specific T Cell Immunity by Anti-DR5 Antibody Therapy |
title_full_unstemmed | Induction of Tumor-specific T Cell Immunity by Anti-DR5 Antibody Therapy |
title_short | Induction of Tumor-specific T Cell Immunity by Anti-DR5 Antibody Therapy |
title_sort | induction of tumor-specific t cell immunity by anti-dr5 antibody therapy |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2211825/ https://www.ncbi.nlm.nih.gov/pubmed/14769851 http://dx.doi.org/10.1084/jem.20031457 |
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