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Targeting of antigens to activated dendritic cells in vivo cures metastatic melanoma in mice

Cancer research. Bd. 65. H. 15. Philadelphia, Pa.: AACR 2005 S. 7007 - 7012

Erscheinungsjahr: 2005

ISBN/ISSN: 0008-5472

Publikationstyp: Zeitschriftenaufsatz

Sprache: Englisch

Doi/URN: 10.1158/0008-5472.CAN-05-0938

Volltext über DOI/URN

Geprüft:Bibliothek

Inhaltszusammenfassung


Anti (alpha)-DEC-205 antibodies target to the DEC-205 receptor that mediates antigen presentation to T cells by dendritic cells. To exploit these properties for immunization purposes, we conjugated the melanoma antigen tyrosinase-related protein (TRP)-2 to alphaDEC-205 antibodies and immunized mice with these conjugates together with dendritic cell-activating oligonucleotides (CpG). Upon injection of the melanoma cell line B16, alphaDEC-TRP immunized mice were protected against tumor growth. ...Anti (alpha)-DEC-205 antibodies target to the DEC-205 receptor that mediates antigen presentation to T cells by dendritic cells. To exploit these properties for immunization purposes, we conjugated the melanoma antigen tyrosinase-related protein (TRP)-2 to alphaDEC-205 antibodies and immunized mice with these conjugates together with dendritic cell-activating oligonucleotides (CpG). Upon injection of the melanoma cell line B16, alphaDEC-TRP immunized mice were protected against tumor growth. Even more important for clinical applications, we were able to substantially slow the growth of implanted B16 cells by injection of alphaDEC-TRP2 conjugates into tumor bearing hosts. Approximately 70% of the animals were cured from existing tumors by treatment with alphaDEC conjugates carrying two different melanoma antigens (TRP-2 and gp100). This protection was due to induction of melanoma-specific CD4 and CD8 responses. Thus, these data show that targeting of dendritic cells in situ by the means of antibody-antigen conjugates may be a novel way to induce long-lasting antitumor immunity.» weiterlesen» einklappen

Autoren


Mahnke, Karsten (Autor)
Qian, Yingjie (Autor)
Fondel, Sabine (Autor)
Brueck, Juergen (Autor)
Becker, Christian (Autor)
Enk, Alexander (Autor)

Klassifikation


DFG Fachgebiet:
2.21 - Mikrobiologie, Virologie und Immunologie

DDC Sachgruppe:
Medizin