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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...

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Autores principales: 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.
Formato: Texto
Lenguaje:English
Publicado: The Rockefeller University Press 2004
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.
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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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