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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16 February 2004
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February 09 2004
Induction of Tumor-specific T Cell Immunity by Anti-DR5 Antibody Therapy
Kazuyoshi Takeda,
Kazuyoshi Takeda
1Department of Immunology, Central Laboratory of Medical Science, Juntendo University School of Medicine, Tokyo 113-8421, Japan
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Noriko Yamaguchi,
Noriko Yamaguchi
1Department of Immunology, Central Laboratory of Medical Science, Juntendo University School of Medicine, Tokyo 113-8421, Japan
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Hisaya Akiba,
Hisaya Akiba
1Department of Immunology, Central Laboratory of Medical Science, Juntendo University School of Medicine, Tokyo 113-8421, Japan
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Yuko Kojima,
Yuko Kojima
2Division of Pathology, Central Laboratory of Medical Science, Juntendo University School of Medicine, Tokyo 113-8421, Japan
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Yoshihiro Hayakawa,
Yoshihiro Hayakawa
3Cancer Immunology Program, Peter MacCallum Cancer Centre, 8006 Victoria, Australia
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Jane E. Tanner,
Jane E. Tanner
3Cancer Immunology Program, Peter MacCallum Cancer Centre, 8006 Victoria, Australia
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Thomas J. Sayers,
Thomas J. Sayers
4Basic Research Program, SAIC-Frederick Inc.
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Naoko Seki,
Naoko Seki
5Laboratory of Experimental Immunology, National Cancer Institute Frederick, Frederick, MD 21702
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Ko Okumura,
Ko Okumura
1Department of Immunology, Central Laboratory of Medical Science, Juntendo University School of Medicine, Tokyo 113-8421, Japan
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Hideo Yagita,
Hideo Yagita
1Department of Immunology, Central Laboratory of Medical Science, Juntendo University School of Medicine, Tokyo 113-8421, Japan
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Mark J. Smyth
Mark J. Smyth
3Cancer Immunology Program, Peter MacCallum Cancer Centre, 8006 Victoria, Australia
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Kazuyoshi Takeda
1Department of Immunology, Central Laboratory of Medical Science, Juntendo University School of Medicine, Tokyo 113-8421, Japan
Noriko Yamaguchi
1Department of Immunology, Central Laboratory of Medical Science, Juntendo University School of Medicine, Tokyo 113-8421, Japan
Hisaya Akiba
1Department of Immunology, Central Laboratory of Medical Science, Juntendo University School of Medicine, Tokyo 113-8421, Japan
Yuko Kojima
2Division of Pathology, Central Laboratory of Medical Science, Juntendo University School of Medicine, Tokyo 113-8421, Japan
Yoshihiro Hayakawa
3Cancer Immunology Program, Peter MacCallum Cancer Centre, 8006 Victoria, Australia
Jane E. Tanner
3Cancer Immunology Program, Peter MacCallum Cancer Centre, 8006 Victoria, Australia
Thomas J. Sayers
4Basic Research Program, SAIC-Frederick Inc.
Naoko Seki
5Laboratory of Experimental Immunology, National Cancer Institute Frederick, Frederick, MD 21702
Ko Okumura
1Department of Immunology, Central Laboratory of Medical Science, Juntendo University School of Medicine, Tokyo 113-8421, Japan
Hideo Yagita
1Department of Immunology, Central Laboratory of Medical Science, Juntendo University School of Medicine, Tokyo 113-8421, Japan
Mark J. Smyth
3Cancer Immunology Program, Peter MacCallum Cancer Centre, 8006 Victoria, Australia
Address correspondence to Kazuyoshi Takeda, Department of Immunology, Juntendo University School of Medicine, 2-1-1 Hongo, Bukyou-ku, Tokyo 113-8421, Japan. Phone: 81-3-3818-9284; Fax: 81-3-3813-0421; email: [email protected]
The online version of this article contains supplemental material.
Abbreviations used in this paper: ADCC, antibody-dependent cellular cytotoxicity; ALT, alanine aminotransferase; ASGM1, asialo-GM1; AST, aspartate aminotransferase; CMA, concanamycin A; FLIP, FLICE inhibitory protein; H/E, hematoxylin/eosin; TRAIL, TNF-related apoptosis-inducing ligand.
Received:
August 25 2003
Accepted:
December 09 2003
Online ISSN: 1540-9538
Print ISSN: 0022-1007
The Rockefeller University Press
2004
J Exp Med (2004) 199 (4): 437–448.
Article history
Received:
August 25 2003
Accepted:
December 09 2003
Citation
Kazuyoshi Takeda, Noriko Yamaguchi, Hisaya Akiba, Yuko Kojima, Yoshihiro Hayakawa, Jane E. Tanner, Thomas J. Sayers, Naoko Seki, Ko Okumura, Hideo Yagita, Mark J. Smyth; Induction of Tumor-specific T Cell Immunity by Anti-DR5 Antibody Therapy . J Exp Med 16 February 2004; 199 (4): 437–448. doi: https://doi.org/10.1084/jem.20031457
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