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

机译:通过具有固有核酸酶活性的3D8 scFv预防C57BL / 6小鼠伪狂犬病病毒感染的治疗策略

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摘要

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 LD50 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.
机译:3D8单链可变片段(scFv)是具有核酸酶活性的重组单克隆抗体,最初是从易发自身免疫性的MRL小鼠中分离出来的。在先前的研究中,我们分析了3D8 scFv的核酸酶活性,并确定表达3D8 scFv的HeLa细胞系赋予了对单纯疱疹病毒1型(HSV-1)和伪狂犬病病毒(PRV)的抗性。在这项研究中,我们证明了3D8 scFv可以被递送到靶组织和细胞中,从而对PRV发挥治疗作用。通过肌内注射接种PRV,并腹膜内注射3D8 scFv。定量逆转录聚合酶链反应,Southern杂交和免疫组织化学分析的结果也证实了3D8 scFv对PRV的治疗效果。腹膜内注射5和10μg3D8 scFv导致未检测到毒性。肌内注射10 LD50 PRV后,C57BL / 6小鼠的存活率为9%。相反,注射3D8 scFv的C57BL / 6小鼠的存活率分别为57%(5μg)和47%(10μg)。结果表明3D8 scFv可以用作几种动物模型中的有效抗病毒剂。

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