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使用溶瘤病毒作为载体的免疫刺激基因疗法。

Immunostimulatory Gene Therapy Using Oncolytic Viruses as Vehicles.

作者信息

Loskog Angelica

机构信息

Department of Immunology, Genetics and Pathology, Science for Life Laboratory, Uppsala University, Rudbeck laboratory C11, Dag Hammarskjoldsvag 20, 75185 Uppsala, Sweden.

Lokon Pharma AB, Dag Hammarskoldsvag 40c, 75183 Uppsala, Sweden.

出版信息

Viruses. 2015 Nov 6;7(11):5780-91. doi: 10.3390/v7112899.

Abstract

Immunostimulatory gene therapy has been developed during the past twenty years. The aim of immunostimulatory gene therapy is to tilt the suppressive tumor microenvironment to promote anti-tumor immunity. Hence, like a Trojan horse, the gene vehicle can carry warriors and weapons into enemy territory to combat the tumor from within. The most promising immune stimulators are those activating and sustaining Th1 responses, but even if potent effects were seen in preclinical models, many clinical trials failed to show objective responses in cancer patients. However, with new tools to control ongoing immunosuppression in cancer patients, immunostimulatory gene therapy is now emerging as an interesting option. In parallel, oncolytic viruses have been shown to be safe in patients. To prolong immune stimulation and to increase efficacy, these two fields are now merging and oncolytic viruses are armed with immunostimulatory transgenes. These novel agents are racing towards approval as established cancer immunotherapeutics.

摘要

免疫刺激基因疗法在过去二十年中得到了发展。免疫刺激基因疗法的目的是改变抑制性肿瘤微环境,以促进抗肿瘤免疫。因此,基因载体就像一匹特洛伊木马,可以将战士和武器带入敌境,从内部对抗肿瘤。最有前景的免疫刺激剂是那些能够激活并维持Th1反应的物质,但即便在临床前模型中观察到了显著效果,许多临床试验仍未能在癌症患者中显示出客观反应。然而,随着控制癌症患者持续免疫抑制的新工具的出现,免疫刺激基因疗法如今正成为一个有吸引力的选择。与此同时,溶瘤病毒已被证明对患者是安全的。为了延长免疫刺激并提高疗效,这两个领域正在融合,溶瘤病毒被装载了免疫刺激转基因。这些新型制剂正竞相获批成为成熟的癌症免疫疗法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1700/4664972/ce5705c172cc/viruses-07-02899-g001.jpg

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