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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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Autores principales: Lee, Gunsup, Cho, SeungChan, Hoang, Phuong Mai, Kim, Dongjun, Lee, Yongjun, Kil, Eui-Joon, Byun, Sung-June, Lee, Taek-Kyun, Kim, Dae-Hyun, Kim, Sunghan, Lee, Sukchan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Korean Society for Molecular and Cellular Biology 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4588720/
https://www.ncbi.nlm.nih.gov/pubmed/26255831
http://dx.doi.org/10.14348/molcells.2015.0073
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author Lee, Gunsup
Cho, SeungChan
Hoang, Phuong Mai
Kim, Dongjun
Lee, Yongjun
Kil, Eui-Joon
Byun, Sung-June
Lee, Taek-Kyun
Kim, Dae-Hyun
Kim, Sunghan
Lee, Sukchan
author_facet Lee, Gunsup
Cho, SeungChan
Hoang, Phuong Mai
Kim, Dongjun
Lee, Yongjun
Kil, Eui-Joon
Byun, Sung-June
Lee, Taek-Kyun
Kim, Dae-Hyun
Kim, Sunghan
Lee, Sukchan
author_sort Lee, Gunsup
collection PubMed
description 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 μg 3D8 scFv resulted in no detectable toxicity. The survival rate in C57BL/6 mice was 9% after intramuscular injection of 10 LD(50) PRV. In contrast, the 3D8 scFv-injected C57BL/6 mice showed survival rates of 57% (5 μg) and 47% (10 μg). The results indicate that 3D8 scFv could be utilized as an effective antiviral agent in several animal models.
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spelling pubmed-45887202015-10-13 Therapeutic Strategy for the Prevention of Pseudorabies Virus Infection in C57BL/6 Mice by 3D8 scFv with Intrinsic Nuclease Activity Lee, Gunsup Cho, SeungChan Hoang, Phuong Mai Kim, Dongjun Lee, Yongjun Kil, Eui-Joon Byun, Sung-June Lee, Taek-Kyun Kim, Dae-Hyun Kim, Sunghan Lee, Sukchan Mol Cells Article 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 μg 3D8 scFv resulted in no detectable toxicity. The survival rate in C57BL/6 mice was 9% after intramuscular injection of 10 LD(50) PRV. In contrast, the 3D8 scFv-injected C57BL/6 mice showed survival rates of 57% (5 μg) and 47% (10 μg). The results indicate that 3D8 scFv could be utilized as an effective antiviral agent in several animal models. Korean Society for Molecular and Cellular Biology 2015-09-30 2015-08-07 /pmc/articles/PMC4588720/ /pubmed/26255831 http://dx.doi.org/10.14348/molcells.2015.0073 Text en © The Korean Society for Molecular and Cellular Biology. All rights reserved. This is an open-access article distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 3.0 Unported License. To view a copy of this license, visit http://creativecommons.org/licenses/by-nc-sa/3.0/.
spellingShingle Article
Lee, Gunsup
Cho, SeungChan
Hoang, Phuong Mai
Kim, Dongjun
Lee, Yongjun
Kil, Eui-Joon
Byun, Sung-June
Lee, Taek-Kyun
Kim, Dae-Hyun
Kim, Sunghan
Lee, Sukchan
Therapeutic Strategy for the Prevention of Pseudorabies Virus Infection in C57BL/6 Mice by 3D8 scFv with Intrinsic Nuclease Activity
title Therapeutic Strategy for the Prevention of Pseudorabies Virus Infection in C57BL/6 Mice by 3D8 scFv with Intrinsic Nuclease Activity
title_full Therapeutic Strategy for the Prevention of Pseudorabies Virus Infection in C57BL/6 Mice by 3D8 scFv with Intrinsic Nuclease Activity
title_fullStr Therapeutic Strategy for the Prevention of Pseudorabies Virus Infection in C57BL/6 Mice by 3D8 scFv with Intrinsic Nuclease Activity
title_full_unstemmed Therapeutic Strategy for the Prevention of Pseudorabies Virus Infection in C57BL/6 Mice by 3D8 scFv with Intrinsic Nuclease Activity
title_short Therapeutic Strategy for the Prevention of Pseudorabies Virus Infection in C57BL/6 Mice by 3D8 scFv with Intrinsic Nuclease Activity
title_sort therapeutic strategy for the prevention of pseudorabies virus infection in c57bl/6 mice by 3d8 scfv with intrinsic nuclease activity
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4588720/
https://www.ncbi.nlm.nih.gov/pubmed/26255831
http://dx.doi.org/10.14348/molcells.2015.0073
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