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Potent neutralizing monoclonal antibodies against Ebola virus infection

机译:效力中和单克隆抗体对埃博拉病毒感染

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Ebola virus infections cause a deadly hemorrhagic disease for which no vaccines or therapeutics has received regulatory approval. Here we show isolation of three (Q206, Q314 and Q411) neutralizing monoclonal antibodies (mAbs) against the surface glycoprotein (GP) of Ebola virus identified in West Africa in 2014 through sequential immunization of Chinese rhesus macaques and antigen-specific single B cell sorting. These mAbs demonstrated potent neutralizing activities against both pseudo and live Ebola virus independent of complement. Biochemical, single particle EM, and mutagenesis analysis suggested Q206 and Q411 recognized novel epitopes in the head while Q314 targeted the glycan cap in the GP1 subunit. Q206 and Q411 appeared to influence GP binding to its receptor NPC1. Treatment with these mAbs provided partial but significant protection against disease in a mouse model of Ebola virus infection. These novel mAbs could serve as promising candidates for prophylactic and therapeutic interventions against Ebola virus infection.
机译:埃博拉病毒感染导致致命的出血疾病,没有疫苗或治疗方法已经获得监管批准。在这里,我们通过连续免疫中国恒河猴和抗原特异性单一B细胞分选,分离在2014年在西非鉴定的艾博拉病毒的表面糖蛋白(GP)的中和的单克隆抗体(MAB)的分离。 。这些MABs展示了与伪和活骨液病毒无关的有效的中和活动。生物化学,单粒子EM和诱变分析建议Q206和Q411识别头部的新型表位,而Q314靶向GP1亚基的甘油帽。 Q206和Q411似乎影响GP与其受体NPC1的结合。用这些mAb治疗为埃博拉病毒感染的小鼠模型提供了局部但重要的疾病保护。这些新的MAB可以作为对埃博拉病毒感染的预防和治疗干预的承诺候选人。

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