Therapeutic Strategy for the Prevention of Pseudorabies Virus Infection in C57BL/6 Mice by 3D8 scFv with Intrinsic Nuclease Activity

3D8 single chain variable fragment (scFv) is a recombinant monoclonal antibody with nuclease activity that was originally isolated from autoimmune-prone MRL mice. In a previous study, we analyzed the nuclease activity of 3D8 scFv and determined that a HeLa cell line expressing 3D8 scFv conferred res...

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Veröffentlicht in:Molecules and cells 2015, 38(9), , pp.773-780
Hauptverfasser: Lee, G., Sungkyunkwan University, Suwon, Republic of Korea, Cho, S.C., Sungkyunkwan University, Suwon, Republic of Korea, Hoang, P.M., Sungkyunkwan University, Suwon, Republic of Korea, Kim, D., Sungkyunkwan University, Suwon, Republic of Korea, Lee, Y., Sungkyunkwan University, Suwon, Republic of Korea, Kil, E.J., Sungkyunkwan University, Suwon, Republic of Korea, Byun, S.J., National Institute of Animal Science, RDA, Suwon, Republic of Korea, Lee, T.K., Korea Institute of Ocean Science and Technology, Geoje, Republic of Korea, Kim, D.H., National Institute of Animal Science, RDA, Suwon, Republic of Korea, Kim, S., Seoul National University, Seoul, Republic of Korea, Lee, S., Sungkyunkwan University, Suwon, Republic of Korea
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Zusammenfassung:3D8 single chain variable fragment (scFv) is a recombinant monoclonal antibody with nuclease activity that was originally isolated from autoimmune-prone MRL mice. In a previous study, we analyzed the nuclease activity of 3D8 scFv and determined that a HeLa cell line expressing 3D8 scFv conferred resistance to herpes simplex virus type 1 (HSV-1) and pseudorabies virus (PRV). In this study, we demonstrate that 3D8 scFv could be delivered to target tissues and cells where it exerted a therapeutic effect against PRV. PRV was inoculated via intramuscular injection, and 3D8 scFv was injected intraperitoneally. The observed therapeutic effect of 3D8 scFv against PRV was also supported by results from quantitative reverse transcription polymerase chain reaction, southern hybridization, and immunohistochemical assays. Intraperitoneal injection of 5 and 10 microgram 3D8 scFv resulted in no detectable toxicity. The survival rate in C57BL/6 mice was 9% after intramuscular injection of 10 LD50 PRV. In contrast, the 3D8 scFv-injected C57BL/6 mice showed survival rates of 57% (5 microgtam) and 47% (10 microgram). The results indicate that 3D8 scFv could be utilized as an effective antiviral agent in several animal models.
ISSN:1016-8478
0219-1032
DOI:10.14348/molcells.2015.0073