Meunier Jean-Christophe, Russell Rodney S, Goossens Vera, Priem Sofie, Walter Hugo, Depla Erik, Union Ann, Faulk Kristina N, Bukh Jens, Emerson Suzanne U, Purcell Robert H
Molecular Hepatitis Section, LID, NIAID, NIH, Bldg. 50, Rm. 6537, 50 South Dr., MSC 8009, Bethesda, MD 20892-8009, USA.
J Virol. 2008 Jan;82(2):966-73. doi: 10.1128/JVI.01872-07. Epub 2007 Oct 31.
The relative importance of humoral and cellular immunity in the prevention or clearance of hepatitis C virus (HCV) infection is poorly understood. However, there is considerable evidence that neutralizing antibodies are involved in disease control. Here we describe the detailed analysis of human monoclonal antibodies (MAbs) directed against HCV glycoprotein E1, which may have the potential to control HCV infection. We have identified two MAbs that can strongly neutralize HCV-pseudotyped particles (HCVpp) bearing the envelope glycoproteins of genotypes 1a, 1b, 4a, 5a, and 6a and less strongly neutralize HCVpp bearing the envelope glycoproteins of genotype 2a. Genotype 3a was not neutralized. The epitopes for both MAbs were mapped to the region encompassing amino acids 313 to 327. In addition, robust neutralization was also observed against cell culture-adapted viruses of genotypes 1a and 2a. Results from this study suggest that these MAbs may have the potential to prevent HCV infection.
体液免疫和细胞免疫在丙型肝炎病毒(HCV)感染的预防或清除中的相对重要性目前还知之甚少。然而,有大量证据表明中和抗体参与了疾病控制。在此,我们描述了针对HCV糖蛋白E1的人单克隆抗体(MAb)的详细分析,这些抗体可能具有控制HCV感染的潜力。我们鉴定出两种单克隆抗体,它们能够强烈中和携带1a、1b、4a、5a和6a基因型包膜糖蛋白的HCV假型颗粒(HCVpp),而对携带2a基因型包膜糖蛋白的HCVpp的中和作用较弱。3a基因型未被中和。两种单克隆抗体的表位均定位在包含氨基酸313至327的区域。此外,对1a和2a基因型的细胞培养适应性病毒也观察到了强大的中和作用。这项研究的结果表明,这些单克隆抗体可能具有预防HCV感染的潜力。