Naik Amruta S, Owsianka Ania, Palmer Brendan A, O'Halloran Ciaran J, Walsh Nicole, Crosbie Orla, Kenny-Walsh Elizabeth, Patel Arvind H, Fanning Liam J
Department of Medicine, University College Cork, Cork, Ireland.
MRC-University of Glasgow Centre for Virus Research, University of Glasgow, Glasgow, United Kingdom.
PLoS One. 2017 May 30;12(5):e0175349. doi: 10.1371/journal.pone.0175349. eCollection 2017.
The humoral immune system responds to chronic hepatitis C virus (HCV) infection by producing neutralising antibodies (nAb). In this study we generated three HCV pseudoparticles in which E1E2 glycoprotein sequence was targeted by the host humoral immune system. We used patient derived virus free Fabs (VF-Fabs) obtained from HCV genotype 1a (n = 3), genotype 1b (n = 7) and genotype 3a (n = 1) for neutralisation of HCVpp produced in this study both individually and in combination. Based on the available anti-HCV monoclonal nAb mapping information we selected amino acid region 384-619 for conformational epitope mapping. Amongst our notable findings, we observed significant reduction in HCVpp infectivity (p<0.05) when challenged with a combination of inter genotype and subtype VF-Fabs. We also identified five binding motifs targeted by patient derived VF-Fab upon peptide mapping, of which two shared the residues with previously reported epitopes. One epitope lies within an immunodominant HVR1 and two were novel. In summary, we used a reverse epitope mapping strategy to identify preferred epitopes by the host humoral immune system. Additionally, we have combined different VF-Fabs to further reduce the HCVpp infectivity. Our data indicates that combining the antigen specificity of antibodies may be a useful strategy to reduce (in-vitro) infectivity.
体液免疫系统通过产生中和抗体(nAb)来应对慢性丙型肝炎病毒(HCV)感染。在本研究中,我们构建了三种HCV假病毒颗粒,其E1E2糖蛋白序列可被宿主体液免疫系统识别。我们使用从HCV 1a型(n = 3)、1b型(n = 7)和3a型(n = 1)患者中获得的无病毒Fab片段(VF-Fab),分别单独及联合用于中和本研究中产生的HCV假病毒颗粒(HCVpp)。基于现有的抗HCV单克隆nAb定位信息,我们选择氨基酸区域384 - 619进行构象表位定位。在我们的显著发现中,当用不同基因型和亚型的VF-Fab联合攻击时,我们观察到HCVpp感染性显著降低(p<0.05)。在肽段定位过程中,我们还鉴定出患者来源的VF-Fab靶向的五个结合基序,其中两个与先前报道的表位共有残基。一个表位位于免疫显性高变区1(HVR1)内,另外两个是新发现的。总之,我们使用反向表位定位策略来鉴定宿主体液免疫系统偏好的表位。此外,我们联合了不同的VF-Fab以进一步降低HCVpp的感染性。我们的数据表明,结合抗体的抗原特异性可能是一种降低(体外)感染性的有效策略。