School of Molecular Medical Sciences, The University of Nottingham, A Floor West Block, Queen's Medical Centre, Nottingham NG7 2UH, United Kingdom.
J Virol. 2011 May;85(9):4246-57. doi: 10.1128/JVI.01332-10. Epub 2011 Feb 16.
Neutralizing antibodies have a role in controlling hepatitis C virus (HCV) infection. A successful vaccine will need to elicit potently neutralizing antibodies that are capable of preventing the infection of genetically diverse viral isolates. However, the specificity of the neutralizing antibody response in natural HCV infection still is poorly understood. To address this, we examined the reactivity of polyclonal antibodies isolated from chronic HCV infection to the diverse patient-isolated HCV envelope glycoproteins E1 and E2 (E1E2), and we also examined the potential to neutralize the entry of pseudoparticles bearing these diverse E1E2 proteins. The genetic type of the infection was found to determine the pattern of the antibody recognition of these E1E2 proteins, with the greatest reactivity to homologous E1E2 proteins. This relationship was strongest when the component of the antibody response directed only to linear epitopes was analyzed. In contrast, the neutralization serotype did not correlate with genotype. Instead, serum-derived antibodies displayed a range of neutralization breadth and potency, while different E1E2 glycoproteins displayed different sensitivities to neutralization, such that these could be divided broadly into neutralization-sensitive and -resistant phenotypes. An important additional observation was that entry mediated by some E1E2 proteins was enhanced in the presence of some of the polyclonal antibody fractions isolated during chronic infection. These data highlight the need to use diverse E1E2 isolates, which represent extremes of neutralization sensitivity, when screening antibodies for therapeutic potential and for testing antibodies generated following immunization as part of vaccine development.
中和抗体在控制丙型肝炎病毒(HCV)感染中发挥作用。成功的疫苗需要诱导能够预防遗传多样性病毒分离株感染的强效中和抗体。然而,在自然 HCV 感染中,中和抗体反应的特异性仍知之甚少。为了解决这个问题,我们研究了从慢性 HCV 感染中分离出的多克隆抗体对不同患者分离的 HCV 包膜糖蛋白 E1 和 E2(E1E2)的反应性,我们还研究了这些不同的 E1E2 蛋白携带的假颗粒进入的中和潜力。感染的遗传类型决定了这些 E1E2 蛋白的抗体识别模式,与同源 E1E2 蛋白的反应性最强。当仅分析针对线性表位的抗体反应成分时,这种关系最强。相比之下,中和血清型与基因型无关。相反,血清来源的抗体显示出广泛的中和广度和效力,而不同的 E1E2 糖蛋白对中和的敏感性不同,因此可以将它们大致分为中和敏感和中和抵抗表型。一个重要的额外观察结果是,在存在慢性感染期间分离出的一些多克隆抗体分数的情况下,某些 E1E2 蛋白介导的进入得到了增强。这些数据强调了在筛选治疗潜力的抗体和测试免疫接种后产生的抗体时,需要使用代表中和敏感性极端的不同 E1E2 分离株,作为疫苗开发的一部分。