发现人类星状病毒囊尖上的三个新型中和抗体表位以及对病毒中和机理的深入了解

Sarah Lanning, Nayeli Aguilar-Hernández, Vitor Hugo Balasco Serrão, Tomás López, Sara M O'Rourke, Adam Lentz, Lena Ricemeyer, Rafaela Espinosa, Susana López, Carlos Federico Arias, Rebecca M. DuBois
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摘要

人类星状病毒(HAstVs)是导致儿童病毒性腹泻的主要原因,几乎每个人一生中都会感染这种病毒。虽然人类哮喘病毒的流行率很高,但目前还没有获得批准的疫苗。抗体反应似乎在保护人们免受 HAstV 感染方面发挥了重要作用,但由于之前只确定了 3 个中和抗体表位,因此缺乏有关中和表位情况的知识。在这里,我们从结构上确定了 3 种未表征的 HAstV 中和单克隆抗体的表位:用 X 射线晶体学方法确定了 2.67 Å 的抗体 4B6,用单粒子低温电子显微镜同时确定了 3.33 Å 的抗体 3H4 和 3B4。我们评估了表位位置与噬菌体尖峰蛋白保守区域的相对关系,发现抗体 4B6 和 3B4 的靶标是 HAstV 尖峰蛋白的上可变环区域,而抗体 3H4 的靶标是尖峰蛋白基部附近的一个新区域,该区域更为保守。此外,我们发现这三种抗体的结合亲和力都很高,它们会与受体FcRn竞争结合到帽状尖峰蛋白上。这些研究为单克隆抗体疗法可以靶向HAstV荚膜的哪些区域提供了信息,有助于合理设计疫苗。
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Discovery of three novel neutralizing antibody epitopes on the human astrovirus capsid spike and mechanistic insights into virus neutralization
Human astroviruses (HAstVs) are a leading cause of viral childhood diarrhea that infect nearly every individual during their lifetime. Although human astroviruses are highly prevalent, no approved vaccine currently exists. Antibody responses appear to play an important role in protection from HAstV infection, however knowledge about the neutralizing epitope landscape is lacking, as only 3 neutralizing antibody epitopes have previously been determined. Here, we structurally define the epitopes of 3 uncharacterized HAstV-neutralizing monoclonal antibodies: antibody 4B6 with X-ray crystallography to 2.67 Å, and antibodies 3H4 and 3B4 simultaneously with single-particle cryogenic-electron microscopy to 3.33 Å. We assess the epitope locations relative to conserved regions on the capsid spike and find that while antibodies 4B6 and 3B4 target the upper variable loop regions of the HAstV spike protein, antibody 3H4 targets a novel region near the base of the spike that is more conserved. Additionally, we found that all 3 antibodies bind with high affinity, and they compete with receptor FcRn binding to the capsid spike. These studies inform which regions of the HAstV capsid can be targeted by monoclonal antibody therapies and could aid in rational vaccine design.
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