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Targeted cytokines for cancer immunotherapy.

Abstract
Targeting of cytokines into the tumor microenvironment using antibody-cytokine fusion proteins, called immunocytokines, represents a novel approach in cancer immunotherapy. This article summarizes therapeutic efficacy and immune mechanisms involved in targeting interleukin-2 (IL-2) to neuroectodermal tumors using ganglioside GD2-specific antibody-IL-2 fusion protein (ch14.18-IL-2). Treatment of established melanoma metastases with ch14.18-IL-2 resulted in eradication of disease followed by a vaccination effect protecting mice from lethal challenges with wild-type tumor calls. In a syngeneic neuroblastoma model, targeted IL-2 was effective in the amplification of a weak memory immune response previously induced by IL-12 gene therapy using an engineered linear version of this heterodimeric cytokine. These findings show that targeted IL-2 may provide an effective tool in cancer immunotherapy and establish the missing link between T cell-mediated vaccination and objective clinical responses.
AuthorsH N Lode, R A Reisfeld
JournalImmunologic research (Immunol Res) Vol. 21 Issue 2-3 Pg. 279-88 ( 2000) ISSN: 0257-277X [Print] United States
PMID10852128 (Publication Type: Journal Article, Research Support, U.S. Gov't, P.H.S.)
Chemical References
  • Interleukin-2
Topics
  • Animals
  • Genetic Therapy
  • Immunotherapy
  • Interleukin-2 (genetics, immunology)
  • Mice
  • Neoplasms (genetics, immunology, therapy)
  • Neoplasms, Experimental (genetics, immunology, therapy)

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