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.
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Authors | H N Lode, R A Reisfeld |
Journal | Immunologic research
(Immunol Res)
Vol. 21
Issue 2-3
Pg. 279-88
( 2000)
ISSN: 0257-277X [Print] United States |
PMID | 10852128
(Publication Type: Journal Article, Research Support, U.S. Gov't, P.H.S.)
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Chemical References |
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Topics |
- Animals
- Genetic Therapy
- Immunotherapy
- Interleukin-2
(genetics, immunology)
- Mice
- Neoplasms
(genetics, immunology, therapy)
- Neoplasms, Experimental
(genetics, immunology, therapy)
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