共 45 条
Fusokine interleukin-2/interleukin-18, a novel potent innate and adaptive immune stimulator with decreased toxicity
被引:13
作者:

Acres, B
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机构: Transgene SA, Mol Immunol Lab, F-67082 Strasbourg, France

Gantzer, M
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机构: Transgene SA, Mol Immunol Lab, F-67082 Strasbourg, France

Remy, C
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机构: Transgene SA, Mol Immunol Lab, F-67082 Strasbourg, France

Futin, N
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h-index: 0
机构: Transgene SA, Mol Immunol Lab, F-67082 Strasbourg, France

Accart, N
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机构: Transgene SA, Mol Immunol Lab, F-67082 Strasbourg, France

Chaloin, O
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机构: Transgene SA, Mol Immunol Lab, F-67082 Strasbourg, France

Hoebeke, J
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机构: Transgene SA, Mol Immunol Lab, F-67082 Strasbourg, France

Balloul, JM
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机构: Transgene SA, Mol Immunol Lab, F-67082 Strasbourg, France

Paul, S
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机构: Transgene SA, Mol Immunol Lab, F-67082 Strasbourg, France
机构:
[1] Transgene SA, Mol Immunol Lab, F-67082 Strasbourg, France
[2] Transgene SA, Div Med & Regulatory Affairs, F-67082 Strasbourg, France
[3] Transgene SA, Histol & Anim Facil Lab, F-67082 Strasbourg, France
[4] CNRS, Inst Biol Mol & Cellulaire, F-67084 Strasbourg, France
关键词:
D O I:
10.1158/0008-5472.CAN-05-0691
中图分类号:
R73 [肿瘤学];
学科分类号:
100214 ;
摘要:
To redress the immune imbalances created by pathologies such as cancer, it would be beneficial to create novel cytokine molecules, which combine desired cytokine activities with reduced toxicities. Due to their divergent but complementary activities, it is of interest to combine interleukin-2 (IL-2) and IL-18 into one recombinant molecule for immunotherapy. Evaluation of a fusokine protein that combines murine IL-2/IL-18 shows that it is stable, maintains IL-2 and IL-18 bioactivities, has notably reduced IL-2 associated toxicities, and has a novel lymphocyte-stimulating activity. An adeno-viral expression system was used to explore the biology of this "fusokine". Inclusion of the IL-18 prosequence (proIL-18) increases the expression, secretion, and potency of this fusokine. In vivo gene transfer experiments show that Ad-IL-2/proIL-18 dramatically outdoes Ad-IL-2, Ad-proIL-18, or the combination of both, by inducing high rates of tumor rejection in several murine models. Both innate and adaptive effector mechanisms are required for this antitumor activity.
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页码:9536 / 9546
页数:11
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