Department of Pathophysiology and Allergy Research, Division of Immunopathology, Center for Pathophysiology, Infectiology and Immunology, Medical University of Vienna, Vienna, Austria.
Institute of Molecular Biosciences, BioTechMed Graz, University of Graz, Graz, Austria.
Sci Rep. 2021 Feb 11;11(1):3551. doi: 10.1038/s41598-021-82893-y.
Human respiratory syncytial virus (RSV) is one of the most important causes of severe respiratory tract infections in early childhood. The only prophylactic protection is the neutralizing antibody, palivizumab, which targets a conformational epitope of the RSV fusion (F) protein. The F protein is generated as a F0 precursor containing two furin cleavage sites allowing excision of the P27 fragment and then gives rise to a fusion-competent version consisting of the N-terminal F2 subunit and the a C-terminal F1 subunits linked by two disulphide bonds. To investigate natural human F-specific antibody responses, F2 conferring the species-specificity of RSV, was expressed in Escherichia coli. Furthermore, the F0 protein, comprising both subunits F2 and F1, was expressed as palivizumab-reactive glycoprotein in baculovirus-infected insect cells. Six overlapping F2-derived peptides lacking secondary structure were synthesized. The analysis of IgG, IgA and IgM responses of adult subjects to native versions and denatured forms of F2 and F0 and to unfolded F2-derived peptides revealed that mainly non-conformational F epitopes, some of which represented cryptic epitopes which are not exposed on the proteins were recognized. Furthermore, we found a dissociation of IgG, IgA and IgM antibody responses to F epitopes with F2 being a major target for the F-specific IgM response. The scattered and dissociated immune response to F may explain why the natural RSV-specific antibody response is only partially protective underlining the need for vaccines focusing human antibody responses towards neutralizing RSV epitopes.
人类呼吸道合胞病毒(RSV)是导致婴幼儿严重呼吸道感染的最重要原因之一。唯一的预防保护措施是中和抗体帕利珠单抗,它针对 RSV 融合(F)蛋白的构象表位。F 蛋白作为含有两个弗林蛋白酶切割位点的 F0 前体产生,允许 P27 片段的切除,然后产生由 N 端 F2 亚基和 C 端 F1 亚基组成的融合有效版本,由两个二硫键连接。为了研究天然人类 F 特异性抗体反应,F2 赋予 RSV 的种特异性,在大肠杆菌中表达。此外,F0 蛋白,包括 F2 和 F1 两个亚基,作为帕利珠单抗反应性糖蛋白在杆状病毒感染的昆虫细胞中表达。合成了六个缺乏二级结构的重叠 F2 衍生肽。分析成人对天然和变性 F2 及 F0 以及展开的 F2 衍生肽的 IgG、IgA 和 IgM 反应,结果表明主要是构象 F 表位被识别,其中一些代表隐藏表位,这些表位在蛋白质上没有暴露。此外,我们发现 F 表位的 IgG、IgA 和 IgM 抗体反应分离,F2 是 F 特异性 IgM 反应的主要靶标。F 的分散和分离的免疫反应可能解释了为什么天然 RSV 特异性抗体反应仅部分具有保护作用,这强调了需要针对中和 RSV 表位的人类抗体反应的疫苗。