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The anaplastic lymphoma kinase is an effective oncoantigen for lymphoma vaccination.

Abstract
An ideal vaccination strategy against tumors relies on specific antigens that are required for tumor maintenance. For lymphoma, vaccination with subject-specific immunoglobulin idiotypes has had the most promising results. Here we show that DNA vaccination with plasmids encoding portions of the cytoplasmic domain of anaplastic lymphoma kinase (ALK), which has been translocated in different fusion proteins necessary for the growth of anaplastic large cell lymphoma (ALCL), protects mice from local and systemic lymphoma growth. The protection is potent and long lasting and elicits ALK-specific interferon-gamma responses and CD8+ T cell-mediated cytotoxicity. A combination of chemotherapy and vaccination significantly enhanced the survival of mice challenged with ALK+ lymphomas. These findings indicate that ALK represents an ideal tumor antigen for vaccination-based therapies of ALCL and possibly other ALK+ human tumors.
AuthorsRoberto Chiarle, Cinzia Martinengo, Cristina Mastini, Chiara Ambrogio, Valentina D'Escamard, Guido Forni, Giorgio Inghirami
JournalNature medicine (Nat Med) Vol. 14 Issue 6 Pg. 676-80 (Jun 2008) ISSN: 1546-170X [Electronic] United States
PMID18469826 (Publication Type: Journal Article, Research Support, N.I.H., Extramural, Research Support, Non-U.S. Gov't)
Chemical References
  • Antigens, Neoplasm
  • Fluorescent Dyes
  • ALK protein, human
  • Alk protein, mouse
  • Anaplastic Lymphoma Kinase
  • Protein-Tyrosine Kinases
  • Receptor Protein-Tyrosine Kinases
  • Fluorescein-5-isothiocyanate
Topics
  • Anaplastic Lymphoma Kinase
  • Animals
  • Antigens, Neoplasm (immunology, therapeutic use)
  • Cell Line, Transformed
  • Cell Line, Tumor
  • Cell Transformation, Neoplastic
  • Fluorescein-5-isothiocyanate (metabolism)
  • Fluorescent Antibody Technique, Direct
  • Fluorescent Dyes (metabolism)
  • Immunization, Secondary
  • Immunohistochemistry
  • Lymphoma, Large-Cell, Anaplastic (immunology, pathology, therapy)
  • Mice
  • Mice, Inbred BALB C
  • Mice, Transgenic
  • Mutation
  • Plasmids
  • Protein-Tyrosine Kinases (genetics, immunology)
  • Receptor Protein-Tyrosine Kinases
  • Vaccination

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