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TNF-alpha and the IFN-gamma-inducible protein 10 (IP-10/CXCL-10) delivered by parvoviral vectors act in synergy to induce antitumor effects in mouse glioblastoma.

Abstract
Interferon-gamma-inducible protein 10 is a potent chemoattractant for natural killer cells and activated T lymphocytes. It also displays angiostatic properties and some antitumor activity. Tumor necrosis factor-alpha (TNF-alpha) is a powerful immunomodulating cytokine with demonstrated tumoricidal activity in various tumor models and the ability to induce strong immune responses. This prompted us to evaluate the antitumor effects of recombinant parvoviruses designed to deliver IP-10 or TNF-alpha into a glioblastoma. When Gl261 murine glioma cells were infected in vitro with an IP-10- or TNF-alpha-transducing parvoviral vector and were subcutaneously implanted in mice, tumor growth was significantly delayed. Complete tumor regression was observed when the glioma cells were coinfected with both the vectors, demonstrating synergistic antitumor activity. In an established in vivo glioma model, however, repeated simultaneous peritumoral injection of the IP-10- and TNF-alpha-delivering parvoviruses failed to improve the therapeutic effect as compared with the use of a single cytokine-delivering vector. In this tumor model, cytokine-mediated immunostimulation, rather than inhibition of vascularization, is likely responsible for the therapeutic efficacy.
AuthorsM Enderlin, E V Kleinmann, S Struyf, C Buracchi, A Vecchi, R Kinscherf, F Kiessling, S Paschek, S Sozzani, J Rommelaere, J J Cornelis, J Van Damme, C Dinsart
JournalCancer gene therapy (Cancer Gene Ther) Vol. 16 Issue 2 Pg. 149-60 (Feb 2009) ISSN: 1476-5500 [Electronic] England
PMID18670452 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
Chemical References
  • CXCL10 protein, human
  • Chemokine CXCL10
  • Tumor Necrosis Factor-alpha
Topics
  • Animals
  • Chemokine CXCL10 (administration & dosage, immunology, metabolism, therapeutic use)
  • Dendritic Cells (cytology, virology)
  • Drug Synergism
  • Female
  • Genetic Vectors
  • Glioblastoma (blood supply, drug therapy, immunology, metabolism, virology)
  • H-1 parvovirus (physiology)
  • Humans
  • Immunocompetence
  • Mice
  • Mice, Inbred C57BL
  • Minute Virus of Mice (physiology)
  • Necrosis (metabolism)
  • Tumor Cells, Cultured (cytology, drug effects)
  • Tumor Necrosis Factor-alpha (administration & dosage, genetics, metabolism, therapeutic use)

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