Abstract
In preclinical models of cancer, gene therapy with interleukin 12 (IL-12) has reached unprecedented levels of success when combined with immunotherapy approaches such as gene transfer of other cytokines and/or chemokines, costimulatory molecules or adoptive cell therapy. These combinations have been found to produce synergistic rather than additive effects. Meanwhile, IL-12 gene therapy is beginning clinical testing as a single agent, but combination strategies are at hand.
Publication types
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News
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Research Support, Non-U.S. Gov't
MeSH terms
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4-1BB Ligand
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Animals
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Antigens, CD / genetics
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Antigens, CD / immunology
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B7-1 Antigen / genetics
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B7-1 Antigen / immunology
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B7-2 Antigen
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Chemokine CXCL10
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Chemokines, CXC / immunology
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Gene Transfer Techniques
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Genetic Therapy*
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Humans
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Immunotherapy* / methods
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Interleukin-12 / genetics
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Interleukin-12 / immunology
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Interleukin-12 / therapeutic use*
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Interleukin-15 / immunology
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Interleukin-18 / immunology
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Interleukin-2 / immunology
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Membrane Glycoproteins / genetics
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Membrane Glycoproteins / immunology
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Mice
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Neoplasms / therapy*
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Tumor Necrosis Factor-alpha / genetics
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Tumor Necrosis Factor-alpha / immunology
Substances
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4-1BB Ligand
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Antigens, CD
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B7-1 Antigen
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B7-2 Antigen
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CD86 protein, human
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Cd86 protein, mouse
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Chemokine CXCL10
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Chemokines, CXC
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Interleukin-15
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Interleukin-18
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Interleukin-2
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Membrane Glycoproteins
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TNFSF9 protein, human
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Tnfsf9 protein, mouse
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Tumor Necrosis Factor-alpha
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Interleukin-12