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从腺病毒病毒组中挖掘针对多种实体瘤的溶瘤病毒。

Mining the adenovirus virome for oncolytics against multiple solid tumor types.

机构信息

Department of Internal Medicine, Mayo Clinic, Rochester, MN, USA.

出版信息

Cancer Gene Ther. 2011 Oct;18(10):744-50. doi: 10.1038/cgt.2011.47. Epub 2011 Sep 2.

Abstract

Although there are 55 serotypes of adenovirus (Ad) that infect humans, Ad serotype 5 (Ad5) is the most widely studied because of the availability of commercial kits for its genetic manipulation. In fact, engineered Ad 5 is currently being used in all of the 87 global clinical trials utilizing Ad for the treatment of cancer. Unfortunately, Ad5 is one of the most seroprevalent serotypes, meaning that this virus has to confront additional immunological barriers to be effective in Ad5-immune patients. In this work, we compare Ad5 to 13 other adenoviral serotypes from species B, C, D and E for oncolytic potential in both immunodeficient mouse and immunocompetent hamster models. Our results indicate that species D Ads are not effective oncolytics against most solid tumors. Conversely, lower seroprevalent Ad6 and Ad11 had anti-cancer activity comparable to Ad5. This work strongly supports the consideration of Ad6-based oncolytic therapies for the treatment of breast, ovarian, kidney and liver tumors.

摘要

虽然有 55 种血清型的腺病毒(Ad)感染人类,但由于其基因操作的商业试剂盒的可用性,Ad 血清型 5(Ad5)是研究最多的。事实上,目前正在使用工程 Ad5 进行全球 87 项利用 Ad 治疗癌症的临床试验。不幸的是,Ad5 是最普遍的血清型之一,这意味着这种病毒在 Ad5 免疫患者中必须面对额外的免疫障碍才能有效。在这项工作中,我们比较了 Ad5 与来自 B、C、D 和 E 种的 13 种其他腺病毒血清型在免疫缺陷小鼠和免疫功能正常的仓鼠模型中的溶瘤潜力。我们的结果表明,D 种 Ads 对大多数实体瘤不是有效的溶瘤剂。相反,血清流行率较低的 Ad6 和 Ad11 具有与 Ad5 相当的抗癌活性。这项工作强烈支持考虑基于 Ad6 的溶瘤疗法来治疗乳腺癌、卵巢癌、肾癌和肝癌。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/275c/3176962/0ddb63608ea6/nihms310885f1.jpg

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