Active specific T-cell-based immunotherapy for cancer: Nucleic acids, peptides, whole native proteins, recombinant viruses, with dendritic cell adjuvants or whole tumor cell-based vaccines. Principles and future prospects

Nadine Fernandez, Marie Thérèse Duffour, Michel Perricaudet, Michael T. Lotze, Thomas Tursz, Laurence Zitvogel

    Résultats de recherche: Contribution à un journalArticleRevue par des pairs

    37 Citations (Scopus)

    Résumé

    Whereas tumor cells are poor immunogens, recombinant tumor cells or dendritic cells as well as engineered viruses have been demonstrated to elicit specific antitumor immune responses leading to tumor growth suppression and long-lasting immunity in mouse tumor models. Single cytotoxic T lymphocyte-defined epitope-based strategies have proved useful for immunization in tumor-bearing mice. This strategy is under investigation in human melanoma, along with adjuvants such as cytokines or dendritic cells. Flt3L is an in vivo dendritic-cell growth factor that offers new prospects in the field of active specific immunotherapy. These immunotherapeutic approaches are being tested in clinical trials, and may open up novel avenues for disease-free patients with poor prognostic factors.

    langue originaleAnglais
    Pages (de - à)53-65
    Nombre de pages13
    journalCytokines, Cellular and Molecular Therapy
    Volume4
    Numéro de publication1
    étatPublié - 1 mars 1998

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