Abd-Elghaffar Asmaa A, Rashed Mohamed E, Ali Amal E, Amin Magdy A
Biotechnology Unit, National Organization for Research and Control of Biological (NORCB), Giza 12654, Egypt.
Bacterial Control Unit, National Organization for Research and Control of Biological (NORCB), Giza 12654, Egypt.
Vaccines (Basel). 2020 Oct 13;8(4):601. doi: 10.3390/vaccines8040601.
After years of global collaboration; we are steps away from a polio-free world. However, the currently conventional inactivated polio vaccine (cIPV) is suboptimal for the post eradication era. cIPV production cost and biosafety hazards hinder its availability and coverage of the global demands. Production of IPV from the attenuated Sabin strains (sIPV) was an ideal solution and scientists work extensively to perfect a safe, effective and affordable sIPV. This study investigated the ability of hydrogen peroxide (HO), ascorbic acid (AA) and epigallocatechin-3-gallate (EGCG) as alternatives for Formaldehyde (HCHO) to inactivate Sabin-polioviruses strains for sIPV production. Sabin-polioviruses vaccine strains were individually treated with AA, EGCG or HO and were compared to HCHO. This was investigated by determination of the inactivation kinetics on HEP cells, testing of D-antigen preservation by ELISA and the immune response in Wistar rats of the four vaccine preparations. HO, AA and EGCG were able to inactivate polioviruses within 24 h while HCHO required 96 h. Significant high D-antigen levels were observed using AA, EGCG and HO compared to HCHO. Rat sera tested for neutralizing antibodies showed comparable results. These findings support the idea of using these inactivating agents as safe and time- saving alternatives for HCHO to produce sIPV.
经过多年的全球合作,我们距离一个无脊髓灰质炎的世界已近在咫尺。然而,目前传统的灭活脊髓灰质炎疫苗(cIPV)在根除后时代并不理想。cIPV的生产成本和生物安全隐患阻碍了其供应以及对全球需求的覆盖。利用减毒的萨宾株生产灭活脊髓灰质炎疫苗(sIPV)是一个理想的解决方案,科学家们进行了广泛研究以完善一种安全、有效且价格合理的sIPV。本研究调查了过氧化氢(HO)、抗坏血酸(AA)和表没食子儿茶素-3-没食子酸酯(EGCG)作为甲醛(HCHO)的替代物灭活萨宾脊髓灰质炎病毒株以生产sIPV的能力。将萨宾脊髓灰质炎病毒疫苗株分别用AA、EGCG或HO处理,并与HCHO处理的进行比较。通过测定在HEP细胞上的灭活动力学、用ELISA检测D抗原的保存情况以及检测四种疫苗制剂在Wistar大鼠体内的免疫反应来进行研究。HO、AA和EGCG能够在24小时内灭活脊髓灰质炎病毒,而HCHO则需要96小时。与HCHO相比,使用AA、EGCG和HO时观察到显著更高的D抗原水平。检测大鼠血清中的中和抗体显示出类似的结果。这些发现支持了使用这些灭活剂作为HCHO的安全且节省时间的替代品来生产sIPV的想法。