Thiyagarajah Keerthihan, Hein Sascha, Raupach Jan, Adeel Nirmal, Miller Johannes, Knapp Maximilian, Welsch Christoph, Glitscher Mirco, Görgülü Esra, Stoffers Philipp, Lembeck Pia, Trebicka Jonel, Ciesek Sandra, Peiffer Kai-Henrik, Hildt Eberhard
Research Group, Paul-Ehrlich-Institute, 63225 Langen, Germany.
Medical Clinic 1, University Hospital, Goethe University Frankfurt, 60329 Frankfurt am Main, Germany.
Viruses. 2025 Sep 7;17(9):1220. doi: 10.3390/v17091220.
The hepatitis D virus (HDV) is a small, defective RNA virus that induces the most severe form of viral hepatitis. Despite its severity, HDV infections are under-diagnosed due to non-standardized and costly diagnostic screening methods. However, limited research has been conducted on characterizing HDV-specific antibodies as alternative tools for diagnosis. Thus, we generated HDV-specific, polyclonal antibodies by immunizing rabbits with the HDV protein, small hepatitis delta antigen (SHDAg), in its oligomeric or denatured form. We identified SHDAg-specific linear epitopes by peptide array analysis and compared them to epitopes identified in HDV-infected patients. Using in silico structural analysis, we show that certain highly immunogenic domains in SHDAg, such as the coiled-coil domain, are masked in the oligomeric conformation of the protein; others, such as the second arginine-rich motif, are exposed. The nuclear localization signal is presumably exposed only by specific interaction of oligomeric HDAg with the HDV-RNA genome. Through surface plasmon resonance analysis, we identified two polyclonal antibodies derived from rabbit antisera with affinities in the lower nanomolar range. These antibodies were used to establish an ELISA that can quantitatively detect HDV virions in vitro and upon further optimization could be used as a promising alternative diagnostic screening method.
丁型肝炎病毒(HDV)是一种小型缺陷RNA病毒,可引发最严重形式的病毒性肝炎。尽管其严重性,但由于诊断筛查方法不规范且成本高昂,HDV感染的诊断不足。然而,关于将HDV特异性抗体作为诊断替代工具的研究有限。因此,我们用HDV蛋白小δ抗原(SHDAg)的寡聚体或变性形式免疫兔子,产生了HDV特异性多克隆抗体。我们通过肽阵列分析鉴定了SHDAg特异性线性表位,并将其与HDV感染患者中鉴定的表位进行比较。通过计算机结构分析,我们表明SHDAg中某些高度免疫原性的结构域,如卷曲螺旋结构域,在蛋白质的寡聚构象中被掩盖;其他结构域,如第二个富含精氨酸的基序,则是暴露的。核定位信号可能仅通过寡聚HDAg与HDV-RNA基因组的特异性相互作用而暴露。通过表面等离子体共振分析,我们从兔抗血清中鉴定出两种亲和力在纳摩尔范围较低的多克隆抗体。这些抗体用于建立一种ELISA,该方法可以在体外定量检测HDV病毒粒子,经过进一步优化后可作为一种有前景的替代诊断筛查方法。