肿瘤坏死因子α
体内
细胞因子
化学
融合蛋白
体外
免疫系统
肽
毒性
细胞生物学
癌症研究
免疫学
生物化学
生物
重组DNA
基因
生物技术
有机化学
作者
Anja Krippner‐Heidenreich,Ingo Grunwald,Gudrun Zimmermann,Marie Kühnle,Jeannette Gerspach,Theobald Sterns,Steven D. Shnyder,Jason H. Gill,Daniela N. Männel,Klaus Pfizenmaier,Peter Scheurich
出处
期刊:Journal of Immunology
[American Association of Immunologists]
日期:2008-06-01
卷期号:180 (12): 8176-8183
被引量:65
标识
DOI:10.4049/jimmunol.180.12.8176
摘要
The inflammatory and proapoptotic cytokine TNF possesses a compelling potential as an antitumoral therapeutic agent. Possible target cells include the malignant cells themselves, the tumor vasculature, or the immune system. As the clinical use of TNF is limited by systemic toxicity, targeting strategies using TNF-based fusion proteins are currently used. A major obstacle, however, is that homotrimeric TNF ligands are prone to activity loss due to dissociation into their monomers. In this study, we report the construction of single-chain TNF molecule, a TNF mutant consisting of three TNF monomers fused by short peptide linkers. In comparison to wild-type TNF, single-chain TNF was found to possess increased stability in vitro and in vivo, displayed reduced systemic toxicity yet slightly enhanced antitumoral activity in mouse models. Creation of single-chain variants is a new approach for improvement of functional activity of therapeutics based on TNF family ligands.
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