Department of Pathology, Microbiology and Immunology, Vanderbilt University, Nashville, United States.
Vanderbilt Vaccine Center, Vanderbilt University Medical Center, Nashville, United States.
Elife. 2023 Mar 27;12:e81743. doi: 10.7554/eLife.81743.
Hantaviruses are high-priority emerging pathogens carried by rodents and transmitted to humans by aerosolized excreta or, in rare cases, person-to-person contact. While infections in humans are relatively rare, mortality rates range from 1 to 40% depending on the hantavirus species. There are currently no FDA-approved vaccines or therapeutics for hantaviruses, and the only treatment for infection is supportive care for respiratory or kidney failure. Additionally, the human humoral immune response to hantavirus infection is incompletely understood, especially the location of major antigenic sites on the viral glycoproteins and conserved neutralizing epitopes. Here, we report antigenic mapping and functional characterization for four neutralizing hantavirus antibodies. The broadly neutralizing antibody SNV-53 targets an interface between Gn/Gc, neutralizes through fusion inhibition and cross-protects against the Old World hantavirus species Hantaan virus when administered pre- or post-exposure. Another broad antibody, SNV-24, also neutralizes through fusion inhibition but targets domain I of Gc and demonstrates weak neutralizing activity to authentic hantaviruses. ANDV-specific, neutralizing antibodies (ANDV-5 and ANDV-34) neutralize through attachment blocking and protect against hantavirus cardiopulmonary syndrome (HCPS) in animals but target two different antigenic faces on the head domain of Gn. Determining the antigenic sites for neutralizing antibodies will contribute to further therapeutic development for hantavirus-related diseases and inform the design of new broadly protective hantavirus vaccines.
汉坦病毒是由啮齿动物携带的高优先级新兴病原体,通过气溶胶化的排泄物传播给人类,在极少数情况下,也会通过人与人之间的接触传播。虽然人类感染的情况相对较少,但死亡率因汉坦病毒的种类而异,范围在 1%至 40%之间。目前,尚无获得美国食品和药物管理局批准的汉坦病毒疫苗或疗法,感染的唯一治疗方法是针对呼吸或肾衰竭的支持性护理。此外,人体对汉坦病毒感染的体液免疫反应尚不完全清楚,特别是病毒糖蛋白上主要抗原表位和保守中和表位的位置。在这里,我们报告了针对四种中和汉坦病毒抗体的抗原定位和功能特征。广泛中和抗体 SNV-53 靶向 Gn/Gc 之间的界面,通过融合抑制中和,并在暴露前或暴露后给药时对旧世界汉坦病毒种汉坦病毒起到交叉保护作用。另一种广泛中和的抗体 SNV-24 也通过融合抑制中和,但靶向 Gc 的结构域 I,并对真实汉坦病毒表现出较弱的中和活性。ANDV 特异性中和抗体(ANDV-5 和 ANDV-34)通过附着阻断中和,并在动物中预防汉坦病毒心肺综合征(HCPS),但靶向 Gn 头部结构域上的两个不同抗原面。确定中和抗体的抗原表位将有助于进一步开发汉坦病毒相关疾病的治疗方法,并为新型广泛保护的汉坦病毒疫苗的设计提供信息。