Pristiwanto Bambang, Rifa'i Muhaimin, Mustafa Irfan, Huyop Fahrul Zaman
Biology Department, Faculty of Mathematics and Natural Sciences, Brawijaya University, Malang, Indonesia.
Biosciences Department, Faculty of Science, Universiti Teknologi Malaysia, 81310 UTM Johor Bahru, Malaysia.
Ann Med Surg (Lond). 2018 Sep 19;35:55-58. doi: 10.1016/j.amsu.2018.09.014. eCollection 2018 Nov.
Epstein-Barr virus (EBV) is closely associated with the high incidence of nasopharyngeal carcinoma in worldwide. Vaccination is one strategy with the potential to prevent the occurrence of EBV-associated cancers, but a suitable vaccine is yet to be licensed. Much vaccine development research focuses on the GP350/220 protein of EBV as it contains an immunogenic epitope at residues 147-165, which efficiently stimulates IgG production . We examined the ability of this epitope (EBVepitope) to induce IgG production in mice.
The antibody binding pattern of the epitope was analyzed using bioinformatics tools. The IgG production in mice were examined by FACS Calibur™ Flow cytometer.
The epitope bound the 72A1 monoclonal antibody at the same site as GP350/220 protein, indicating that the epitope should stimulate B cells to produce antibody. Moreover, administration of EBVepitope successfully induced IgG expression from B cells, compared with controls. Further investigation indicated that the relative number of B cells expressing IgE in EBVepitope-treated mice was lower than controls.
Our data suggest that this EBV GP350 epitope is able to induce IgG expression without causing allergic reactions, and represents a potential EBV vaccine candidate.
爱泼斯坦-巴尔病毒(EBV)与全球范围内鼻咽癌的高发病率密切相关。疫苗接种是预防EBV相关癌症发生的一种潜在策略,但尚未有合适的疫苗获得许可。许多疫苗研发研究聚焦于EBV的GP350/220蛋白,因为它在147 - 165位残基处含有一个免疫原性表位,能有效刺激IgG产生。我们研究了这个表位(EBV表位)在小鼠体内诱导IgG产生的能力。
使用生物信息学工具分析该表位的抗体结合模式。通过FACS Calibur™流式细胞仪检测小鼠体内的IgG产生情况。
该表位与72A1单克隆抗体的结合位点与GP350/220蛋白相同,表明该表位应能刺激B细胞产生抗体。此外,与对照组相比,给予EBV表位成功诱导了B细胞表达IgG。进一步研究表明,经EBV表位处理的小鼠中表达IgE的B细胞相对数量低于对照组。
我们的数据表明,这种EBV GP350表位能够诱导IgG表达而不引起过敏反应,代表了一种潜在的EBV疫苗候选物。