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In Vivo Time-Related Evaluation of a Therapeutic Neutralization Monoclonal Antibody against Lethal Enterovirus 71 Infection in a Mouse Model

机译:小鼠模型中的致死性肠道病毒71感染的治疗中和单克隆抗体的体内时间相关评价。

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摘要

Enterovirus 71 (EV71) is a neurotropic virus capable of inducing severe neurological symptoms and death. No direct targeting antivirals are useful in the treatment of severe EV71 infection. Because of low toxicity and good specificity, monoclonal antibodies (MAb) are a potential candidate for the treatment of viral infections. Therefore, we developed an EV71-specific conformational MAb with high in vitro cross-neutralization activity to heterologous EV71 subgenotypes. The in vivo treatment experiment at different days post-infection indicated that a single treatment of MAb CT11F9 within day 3 post-infection fully protected mice from morbidity and mortality (0% PBS vs. 100% at 10 µg/g per body weight ***P<0.0001). Immunohistochemical and histological analysis confirmed that CT11F9 significantly prohibited EV71 VP1 expression in various tissues and prevented EV71-induced myonecrosis. Moreover, thrice-treatment at day 4, 5, 6 post-infection was associated with an increased survival rate (18.2% single vs. 50% thrice at 20 µg/g per body weight), and the mice recovered from limb paralysis. Competitive ELISA also confirmed that CT11F9-recognized epitopes were immunodominant in humans. In conclusion, MAb CT11F9 is an ideal candidate to be humanized and used in severe EV71 infection.
机译:肠病毒71(EV71)是一种神经营养性病毒,能够引起严重的神经系统症状和死亡。没有直接靶向的抗病毒药可用于治疗严重的EV71感染。由于低毒性和良好的特异性,单克隆抗体(MAb)是治疗病毒感染的潜在候选药物。因此,我们开发了对异源EV71亚基因型具有高体外交叉中和活性的EV71特异性构象单克隆抗体。感染后不同天的体内治疗实验表明,在感染后第3天单次治疗MAb CT11F9可以完全保护小鼠免于发病和死亡(0%PBS与100%,每体重10 µg / g ** * P <0.0001)。免疫组织化学和组织学分析证实,CT11F9显着抑制了EV71 VP1在各种组织中的表达,并预防了EV71引起的心肌坏死。此外,在感染后第4、5、6天进行三次处理可提高存活率(单重为18.2%,每体重20 µg / g则为50%三次),小鼠从肢体瘫痪中康复。竞争性ELISA也证实了CT11F9识别的表位在人体中具有免疫优势。总之,单克隆抗体CT11F9是理想的人源化抗体,可用于严重的EV71感染。

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