Department of Molecular Microbiology, Washington University School of Medicine, St Louis, Missouri, United States of America.
PLoS Pathog. 2013;9(4):e1003312. doi: 10.1371/journal.ppat.1003312. Epub 2013 Apr 18.
Chikungunya virus (CHIKV) is a mosquito-transmitted alphavirus that causes global epidemics of a debilitating polyarthritis in humans. As there is a pressing need for the development of therapeutic agents, we screened 230 new mouse anti-CHIKV monoclonal antibodies (MAbs) for their ability to inhibit infection of all three CHIKV genotypes. Four of 36 neutralizing MAbs (CHK-102, CHK-152, CHK-166, and CHK-263) provided complete protection against lethality as prophylaxis in highly susceptible immunocompromised mice lacking the type I IFN receptor (Ifnar(-/-) ) and mapped to distinct epitopes on the E1 and E2 structural proteins. CHK-152, the most protective MAb, was humanized, shown to block viral fusion, and require Fc effector function for optimal activity in vivo. In post-exposure therapeutic trials, administration of a single dose of a combination of two neutralizing MAbs (CHK-102+CHK-152 or CHK-166+CHK-152) limited the development of resistance and protected immunocompromised mice against disease when given 24 to 36 hours before CHIKV-induced death. Selected pairs of highly neutralizing MAbs may be a promising treatment option for CHIKV in humans.
基孔肯雅病毒(CHIKV)是一种通过蚊子传播的甲病毒,可导致人类出现严重的多发性关节炎全球流行。由于迫切需要开发治疗药物,我们筛选了 230 种新的抗 CHIKV 单克隆抗体(MAb),以评估它们抑制所有三种 CHIKV 基因型感染的能力。在高度易感的免疫功能低下缺乏 I 型干扰素受体(Ifnar(-/-))的小鼠中,有 4 种中和 MAb(CHK-102、CHK-152、CHK-166 和 CHK-263)可作为预防措施完全阻止致死性,这些 MAb 针对 E1 和 E2 结构蛋白上的不同表位。CHK-152 是最具保护作用的 MAb,它被人源化,可阻断病毒融合,并需要 Fc 效应功能才能在体内发挥最佳活性。在暴露后治疗试验中,在 CHIKV 诱导死亡前 24 至 36 小时给予两种中和 MAb(CHK-102+CHK-152 或 CHK-166+CHK-152)的单一剂量组合可限制耐药性的发展,并保护免疫功能低下的小鼠免受疾病影响。选择高度中和的 MAb 对人类 CHIKV 可能是一种有前途的治疗选择。