An immunotoxin targeting Ebola virus glycoprotein inhibits Ebola virus production from infected cells.
Yingyun CaiShuiqing YuXiaoli ChiSheli R RadoshitzkyJ Thomas BeattyEdward A BergerPublished in: PloS one (2021)
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.
Keyphrases
- induced apoptosis
- cell cycle arrest
- pseudomonas aeruginosa
- randomized controlled trial
- oxidative stress
- endoplasmic reticulum stress
- monoclonal antibody
- signaling pathway
- healthcare
- escherichia coli
- cell death
- cancer therapy
- staphylococcus aureus
- drug delivery
- machine learning
- pi k akt
- electronic health record
- acinetobacter baumannii