| Literature DB >> 33411835 |
Yingyun Cai1, Shuiqing Yu1, Xiaoli Chi2,3, Sheli R Radoshitzky2,3, Jens H Kuhn1, Edward A Berger4.
Abstract
Ebola virus (EBOV), a member of the mononegaviral family Filoviridae, causes severe disease associated with high lethality in humans. Despite enormous progress in development of EBOV medical countermeasures, no anti-EBOV treatment has been approved. We designed an immunotoxin in which a single-chain variable region fragment of the EBOV glycoprotein-specific monoclonal antibody 6D8 was fused to the effector domains of Pseudomonas aeruginosa exotoxin A (PE38). This immunotoxin, 6D8-PE38, bound specifically to cells expressing EBOV glycoproteins. Importantly, 6D8-PE38 targeted EBOV-infected cells, as evidenced by inhibition of infectious EBOV production from infected cells, including primary human macrophages. The data presented here provide a proof of concept for immunotoxin-based targeted killing of infected cells as a potential antiviral intervention for Ebola virus disease.Entities:
Year: 2021 PMID: 33411835 PMCID: PMC7790382 DOI: 10.1371/journal.pone.0245024
Source DB: PubMed Journal: PLoS One ISSN: 1932-6203 Impact factor: 3.240