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Technology transfer of oil-in-water emulsion adjuvant manufacturing for pandemic influenza vaccine production in Romania: Preclinical evaluation of split virion inactivated H5N1 vaccine with adjuvant

机译:罗马尼亚生产用于大流行性流感疫苗的水包油型乳剂佐剂的技术转让:分裂的病毒体灭活的H5N1佐剂疫苗的临床前评估

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摘要

Millions of seasonal and pandemic influenza vaccine doses containing oil-in-water emulsion adjuvant have been administered in order to enhance and broaden immune responses and to facilitate antigen sparing. Despite the enactment of a Global Action Plan for Influenza Vaccines and a multi-fold increase in production capabilities over the past 10 years, worldwide capacity for pandemic influenza vaccine production is still limited. In developing countries, where routine influenza vaccination is not fully established, additional measures are needed to ensure adequate supply of pandemic influenza vaccines without dependence on the shipment of aid from other, potentially impacted first-world countries. Adaptation of influenza vaccine and adjuvant technologies by developing country influenza vaccine manufacturers may enable antigen sparing and corresponding increases in global influenza vaccine coverage capacity. Following on previously described work involving the technology transfer of oil-in-water emulsion adjuvant manufacturing to a Romanian vaccine manufacturing institute, we herein describe the preclinical evaluation of inactivated split virion H5N1 influenza vaccine with emulsion adjuvant, including immunogenicity, protection from virus challenge, antigen sparing capacity, and safety. In parallel with the evaluation of the bioactivity of the tech-transferred adjuvant, we also describe the impact of concurrent antigen manufacturing optimization activities. Depending on the vaccine antigen source and manufacturing process, inclusion of adjuvant was shown to enhance and broaden functional antibody titers in mouse and rabbit models, promote protection from homologous virus challenge in ferrets, and facilitate antigen sparing. Besides scientific findings, the operational lessons learned are delineated in order to facilitate adaptation of adjuvant technologies by other developing country institutes to enhance global pandemic influenza preparedness.
机译:已经施用了数百万种含有水包油乳剂佐剂的季节性和大流行性流感疫苗,以增强和扩大免疫应答并促进抗原节约。尽管已制定了《全球流感疫苗行动计划》,并且在过去十年中生产能力已成倍增长,但全球大流行性流感疫苗的生产能力仍然有限。在尚未完全建立常规流感疫苗的发展中国家,需要采取其他措施来确保足够的大流行性流感疫苗供应,而不依赖于其他可能受到影响的第一世界国家运送的援助。发展中国家流感疫苗制造商对流感疫苗和佐剂技术的适应可能会节省抗原,并相应增加全球流感疫苗的覆盖能力。在先前涉及将水包油乳液佐剂制造技术转移到罗马尼亚疫苗制造研究所的工作之后,我们在此描述了带有乳液佐剂的灭活分裂病毒粒子H5N1流感疫苗的临床前评估,包括免疫原性,抗病毒攻击,抗原保留能力强,安全性高。在评估技术转让的佐剂的生物活性的同时,我们还描述了同时进行的抗原制造优化活性的影响。根据疫苗抗原的来源和生产工艺,佐剂的添加可增强和拓宽小鼠和兔子模型中的功能抗体效价,促进对雪貂免受同源病毒攻击的保护,并促进抗原节约。除科​​学发现外,还介绍了所汲取的实际操作经验,以利于其他发展中国家机构采用辅助技术来增强全球大流行性流感的防范能力。

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