Department of Medicine, Johns Hopkins University School of Medicine, Baltimore, MD 21205.
Division of Biology and Biological Engineering, California Institute of Technology, Pasadena, CA 91125.
Proc Natl Acad Sci U S A. 2018 Jan 2;115(1):E82-E91. doi: 10.1073/pnas.1718441115. Epub 2017 Dec 18.
There is an urgent need for a vaccine to combat the hepatitis C virus (HCV) pandemic, and induction of broadly neutralizing monoclonal antibodies (bNAbs) against HCV is a major goal of vaccine development. Even within HCV genotype 1, no single bNAb effectively neutralizes all viral strains, so induction of multiple neutralizing monoclonal antibodies (NAbs) targeting distinct epitopes may be necessary for protective immunity. Therefore, identification of optimal NAb combinations and characterization of NAb interactions can guide vaccine development. We analyzed neutralization profiles of 12 human NAbs across diverse HCV strains, assigning the NAbs to two functionally distinct clusters. We then measured neutralizing breadth of 35 NAb combinations against genotype 1 isolates, with each combination including one NAb from each neutralization cluster. Many NAbs displayed complementary neutralizing breadth, forming combinations with greater neutralization across diverse strains than any individual bNAb. Remarkably, one of the most broadly neutralizing combinations of two NAbs, designated HEPC74/HEPC98, also displayed enhanced potency, with interactions matching the Bliss independence model, suggesting that these NAbs inhibit HCV infection through independent mechanisms. Subsequent experiments showed that HEPC74 primarily blocks HCV envelope protein binding to CD81, while HEPC98 primarily blocks binding to scavenger receptor B1 and heparan sulfate. Together, these data identify a critical vulnerability resulting from the reliance of HCV on multiple cell surface receptors, suggesting that vaccine induction of multiple NAbs with distinct neutralization profiles is likely to enhance the breadth and potency of the humoral immune response against HCV.
目前迫切需要一种能够对抗丙型肝炎病毒 (HCV) 大流行的疫苗,而诱导针对 HCV 的广泛中和单克隆抗体 (bNAb) 是疫苗开发的主要目标。即使在 HCV 基因型 1 中,也没有单一的 bNAb 能有效地中和所有病毒株,因此诱导针对不同表位的多种中和性单克隆抗体 (NAb) 可能是保护性免疫所必需的。因此,确定最佳的 NAb 组合并表征 NAb 相互作用可以指导疫苗的开发。我们分析了 12 种针对不同 HCV 株的人源 NAb 的中和谱,将这些 NAb 分为两个功能上不同的簇。然后,我们测量了针对基因型 1 分离株的 35 种 NAb 组合的中和广度,每种组合都包含来自每个中和簇的一种 NAb。许多 NAb 表现出互补的中和广度,形成的组合对不同株的中和作用比任何单个 bNAb 都广泛。值得注意的是,两种 NAb 组成的最广泛中和的组合之一,命名为 HEPC74/HEPC98,也显示出增强的效力,其相互作用符合 Bliss 独立性模型,这表明这些 NAb 通过独立的机制抑制 HCV 感染。随后的实验表明,HEPC74 主要阻断 HCV 包膜蛋白与 CD81 的结合,而 HEPC98 主要阻断与清道夫受体 B1 和硫酸乙酰肝素的结合。总之,这些数据确定了 HCV 对多种细胞表面受体的依赖所产生的一个关键弱点,表明疫苗诱导具有不同中和谱的多种 NAb 可能会增强针对 HCV 的体液免疫反应的广度和效力。