Engineering oncolytic vaccinia virus to redirect macrophages to tumor cells

Felicia Cao, Phuong Nguyen, Bangxing Hong, Christopher DeRenzo, Nino C. Rainusso, Tania Rodriguez Cruz, Meng-Fen Wu, Hao Liu, Xiao-Tong Song, Masataka Suzuki, Lisa L. Wang, Jason T. Yustein, Stephen Gottschalk
{"title":"Engineering oncolytic vaccinia virus to redirect macrophages to tumor cells","authors":"Felicia Cao,&nbsp;Phuong Nguyen,&nbsp;Bangxing Hong,&nbsp;Christopher DeRenzo,&nbsp;Nino C. Rainusso,&nbsp;Tania Rodriguez Cruz,&nbsp;Meng-Fen Wu,&nbsp;Hao Liu,&nbsp;Xiao-Tong Song,&nbsp;Masataka Suzuki,&nbsp;Lisa L. Wang,&nbsp;Jason T. Yustein,&nbsp;Stephen Gottschalk","doi":"10.1002/acg2.99","DOIUrl":null,"url":null,"abstract":"<p>Oncolytic virotherapy has been tested in numerous early phase clinical studies. However, the antitumor activity of oncolytic viruses thus far has been limited. Numerous strategies are being explored to enhance their antitumor activity by activating the adaptive arm of the immune system. We reasoned that it might also be possible to engineer oncolytic viruses to redirect tumor-associated macrophages to tumor cells for therapeutic benefit. We engineered an oncolytic vaccinia virus (VV) to disrupt the CD47/SIRPα interaction by expressing a chimeric molecule that consists of the ectodomain of SIRPα and the Fc domain of IgG4 (SIRPα-Fc-VV). SIRPα-Fc-VV readily replicated in tumor cells and redirected M1 as well as M2 macrophages to tumor cells in vitro. In contrast, control VVs that either encoded YFP (YFP-VV) or SIRPα (SIRPα-VV) did not. In vivo, SIRPα-Fc-VV had greater antitumor activity than YFP-VV and SIRPα-VV in an immune competent osteosarcoma model resulting in a significant survival advantage. Pretreatment with cytoxan further augmented the antitumor activity of SIRPα-Fc-VV. Thus, arming oncolytic viruses with SIRPα-Fc may present a promising strategy to enhance their antitumor activity for the virotherapy of solid tumors.</p>","PeriodicalId":72084,"journal":{"name":"Advances in cell and gene therapy","volume":null,"pages":null},"PeriodicalIF":0.0000,"publicationDate":"2020-07-03","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1002/acg2.99","citationCount":"10","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Advances in cell and gene therapy","FirstCategoryId":"1085","ListUrlMain":"https://onlinelibrary.wiley.com/doi/10.1002/acg2.99","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 10

Abstract

Oncolytic virotherapy has been tested in numerous early phase clinical studies. However, the antitumor activity of oncolytic viruses thus far has been limited. Numerous strategies are being explored to enhance their antitumor activity by activating the adaptive arm of the immune system. We reasoned that it might also be possible to engineer oncolytic viruses to redirect tumor-associated macrophages to tumor cells for therapeutic benefit. We engineered an oncolytic vaccinia virus (VV) to disrupt the CD47/SIRPα interaction by expressing a chimeric molecule that consists of the ectodomain of SIRPα and the Fc domain of IgG4 (SIRPα-Fc-VV). SIRPα-Fc-VV readily replicated in tumor cells and redirected M1 as well as M2 macrophages to tumor cells in vitro. In contrast, control VVs that either encoded YFP (YFP-VV) or SIRPα (SIRPα-VV) did not. In vivo, SIRPα-Fc-VV had greater antitumor activity than YFP-VV and SIRPα-VV in an immune competent osteosarcoma model resulting in a significant survival advantage. Pretreatment with cytoxan further augmented the antitumor activity of SIRPα-Fc-VV. Thus, arming oncolytic viruses with SIRPα-Fc may present a promising strategy to enhance their antitumor activity for the virotherapy of solid tumors.

查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
工程溶瘤痘苗病毒将巨噬细胞重定向到肿瘤细胞
溶瘤病毒疗法已经在许多早期临床研究中进行了测试。然而,迄今为止,溶瘤病毒的抗肿瘤活性有限。许多策略正在探索通过激活免疫系统的适应性臂来增强其抗肿瘤活性。我们推断,设计溶瘤病毒将肿瘤相关巨噬细胞重定向到肿瘤细胞中以获得治疗益处也是可能的。我们设计了一种溶瘤痘苗病毒(VV),通过表达由SIRPα的外畴和IgG4的Fc结构域(SIRPα-Fc-VV)组成的嵌合分子来破坏CD47/SIRPα的相互作用。SIRPα-Fc-VV在体外很容易在肿瘤细胞中复制,并将M1和M2巨噬细胞重定向到肿瘤细胞。相比之下,编码YFP (YFP- vv)或SIRPα (SIRPα- vv)的对照vv则不编码。在体内,在免疫能力骨肉瘤模型中,SIRPα-Fc-VV比YFP-VV和SIRPα-VV具有更强的抗肿瘤活性,具有显著的生存优势。环磷酰胺预处理进一步增强了SIRPα-Fc-VV的抗肿瘤活性。因此,用SIRPα-Fc武装溶瘤病毒可能是一种很有前途的策略,可以增强它们在实体瘤病毒治疗中的抗肿瘤活性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 去求助
来源期刊
自引率
0.00%
发文量
0
期刊最新文献
Silencing of B4Galnt1 Gene Prevents GM2 Accumulation in Tay-Sachs Cells Induction of Exocytosis Rescues Lysosomal GM2 Accumulation in Tay-Sachs Disease Therapeutic Effect of Hydrodynamics-Based Delivery of Matrix Metalloproteinase-13 Gene on Thioacetamide-Induced Liver Fibrosis in Rats Intra-Articular AAV9 α-l-Iduronidase Gene Replacement in the Canine Model of Mucopolysaccharidosis Type I Diagnostic and Therapeutic Application of Proteomics in Infectious Disease
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1