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A Neutralizing Monoclonal Antibody Targeting the Acid-Sensitive Region in Chikungunya Virus E2 Protects from Disease

机译:靶向基孔肯雅病毒E2酸敏感区的中和单克隆抗体可预防疾病

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摘要

The mosquito-borne alphavirus, chikungunya virus (CHIKV), has recently reemerged, producing the largest epidemic ever recorded for this virus, with up to 6.5 million cases of acute and chronic rheumatic disease. There are currently no licensed vaccines for CHIKV and current anti-inflammatory drug treatment is often inadequate. Here we describe the isolation and characterization of two human monoclonal antibodies, C9 and E8, from CHIKV infected and recovered individuals. C9 was determined to be a potent virus neutralizing antibody and a biosensor antibody binding study demonstrated it recognized residues on intact CHIKV VLPs. Shotgun mutagenesis alanine scanning of 98 percent of the residues in the E1 and E2 glycoproteins of CHIKV envelope showed that the epitope bound by C9 included amino-acid 162 in the acid-sensitive region (ASR) of the CHIKV E2 glycoprotein. The ASR is critical for the rearrangement of CHIKV E2 during fusion and viral entry into host cells, and we predict that C9 prevents these events from occurring. When used prophylactically in a CHIKV mouse model, C9 completely protected against CHIKV viremia and arthritis. We also observed that when administered therapeutically at 8 or 18 hours post-CHIKV challenge, C9 gave 100% protection in a pathogenic mouse model. Given that targeting this novel neutralizing epitope in E2 can potently protect both in vitro and in vivo, it is likely to be an important region both for future antibody and vaccine-based interventions against CHIKV.
机译:蚊子传播的甲型病毒基孔肯雅病毒(CHIKV)最近重新流行,产生了有史以来最大的这种病毒的流行病,多达650万例急慢性风湿病。目前尚无用于CHIKV的许可疫苗,并且当前的抗炎药治疗常常不足。在这里,我们描述了从CHIKV感染和恢复的个体中分离和表征两种人类单克隆抗体C9和E8。 C9被确定为有效的病毒中和抗体,生物传感器抗体结合研究表明C9可以识别完整的CHIKV VLP上的残基。 gun弹枪诱变丙氨酸扫描CHIKV包膜的E1和E2糖蛋白中98%的残基显示,C9结合的表位在CHIKV E2糖蛋白的酸敏感区(ASR)中包含氨基酸162。 ASR对于融合和病毒进入宿主细胞过程中CHIKV E2的重排至关重要,并且我们预测C9会阻止这些事件的发生。当预防性地用于CHIKV小鼠模型中时,C9可以完全抵抗CHIKV病毒血症和关节炎。我们还观察到,在Chikv攻击后8或18小时进行治疗性给药时,C9在致病性小鼠模型中提供了100%的保护。鉴于靶向E2中这种新颖的中和表位可以有效地保护体内和体外,因此它可能是未来针对CHIKV的抗体和基于疫苗的干预措施的重要领域。

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