Skip NavigationSkip to Content

Induction of tumor-specific T cell immunity by anti-DR5 antibody therapy

  1. Author:
    Takeda, K.
    Yamaguchi, N.
    Akiba, H.
    Kojima, Y.
    Hayakawa, Y.
    Tanner, J. E.
    Sayers, T. J.
    Seki, N.
    Okumura, K.
    Yagita, H.
    Smyth, M. J.
  2. Author Address

    Takeda, K, Juntendo Univ, Sch Med, Dept Immunol, Bukyou Ku, 2-1-1 Hongo, Tokyo 1138421, Japan Juntendo Univ, Sch Med, Dept Immunol, Bukyou Ku, Tokyo 1138421, Japan. Juntendo Univ, Sch Med, Div Pathol, Cent Lab Med Sci,Bukyou Ku, Tokyo 1138421, Japan. Peter MacCallum Canc Ctr, Canc Immunol Program, Melbourne, Vic 8006, Australia. SAIC Frederick Inc, Basic Res Program, Frederick, MD 21702 USA. NCI, Expt Immunol Lab, Frederick, MD 21702 USA.
    1. Year: 2004
  1. Journal: Journal of Experimental Medicine
    1. 199
    2. 4
    3. Pages: 437-448
  2. Type of Article: Article
  1. Abstract:

    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 DFG 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

    See More

External Sources

  1. No sources found.

Library Notes

  1. No notes added.
NCI at Frederick

You are leaving a government website.

This external link provides additional information that is consistent with the intended purpose of this site. The government cannot attest to the accuracy of a non-federal site.

Linking to a non-federal site does not constitute an endorsement by this institution or any of its employees of the sponsors or the information and products presented on the site. You will be subject to the destination site's privacy policy when you follow the link.

ContinueCancel