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基于萨宾株的灭活脊髓灰质炎病毒疫苗的研发:进展报告。

Development of inactivated poliovirus vaccine from Sabin strains: A progress report.

作者信息

Okayasu Hiromasa, Sein Carolyn, Hamidi Ahd, Bakker Wilfried A M, Sutter Roland W

机构信息

Research and Product Development Team, Polio Eradication Department, The World Health Organization, Geneva, Switzerland.

Research and Product Development Team, Polio Eradication Department, The World Health Organization, Geneva, Switzerland.

出版信息

Biologicals. 2016 Nov;44(6):581-587. doi: 10.1016/j.biologicals.2016.08.005. Epub 2016 Oct 5.

Abstract

The Global Polio Eradication Initiative (GPEI) has seen significant progress since it began in 1988, largely due to the worldwide use of oral poliovirus vaccine (OPV). In order to achieve polio eradication the global cessation of OPV is necessary because OPV contains live attenuated poliovirus, which in rare circumstances could re-gain wild poliovirus (WPV) characteristics with potential to establish transmission. The GPEI endgame strategy for the period 2013-2018 recommends the globally synchronised sequential cessation of the Sabin strains contained in the OPV, starting with type 2 Sabin. The withdrawal of Sabin type 2 took place in April 2016, with the introduction of at least one dose of inactivated poliovirus vaccine (IPV) as a risk mitigation strategy. The introduction of IPV into 126 countries since 2013 has required a rapid scale-up of IPV production by the two manufacturers supplying the global public sector market. This scale-up has been fraught with challenges, resulting in reductions of 40-50% of initial supply commitments. Consequently, 22 countries will not be supplied until 2018, and another 23 countries will experience serious stock-outs. In the last decade repeated calls-for-action were made to the global community to invigorate their vision and investment in developing "new poliovirus vaccines" including the development of IPV from less-virulent strains, such as Sabin-IPV (S-IPV). The conventional Salk-IPV production is limited to high-income industrialized-country manufacturers due to the containment requirements (i.e., high sanitation, low force-of-poliovirus-infection, and high population immunity). The use of Sabin strains in the production of S-IPV carries a lower biosafety risk, and was determined to be suitable for production in developing countries, expanding the manufacturing base and making IPV more affordable and accessible in the long term. Significant progress in the S-IPV has been made since 2006. S-IPV is now licensed as S-IPV in Japan and as standalone S-IPV in China, demonstrating the feasibility of this vaccine. In addition, production process improvements can further reduce the cost of production. The latter are critical to the economic success of this vaccine in the global market. We summarize the progress made to date in S-IPV technology, the scientific data and economic evidence in support of S-IPV development.

摘要

全球根除脊髓灰质炎行动(GPEI)自1988年启动以来已取得显著进展,这在很大程度上归功于口服脊髓灰质炎疫苗(OPV)在全球范围内的使用。为了实现根除脊髓灰质炎的目标,全球必须停止使用OPV,因为OPV含有减毒活脊髓灰质炎病毒,在极少数情况下,这种病毒可能重新获得野生脊髓灰质炎病毒(WPV)的特性并有可能引发传播。GPEI 2013 - 2018年的终局战略建议在全球范围内同步逐步停用OPV中所含的萨宾毒株,首先从2型萨宾毒株开始。2016年4月停用了2型萨宾毒株,并引入了至少一剂灭活脊髓灰质炎疫苗(IPV)作为降低风险的策略。自2013年以来,在向126个国家引入IPV的过程中,为全球公共部门市场供货的两家制造商需要迅速扩大IPV的生产规模。这种扩大规模充满挑战,导致初始供应承诺减少了40% - 50%。因此,22个国家要到2018年才能获得供应,另外23个国家将面临严重的库存短缺。在过去十年里,曾多次呼吁国际社会重振其愿景并加大对开发“新型脊髓灰质炎疫苗”的投资,包括从毒性较低的毒株研发IPV,如萨宾IPV(S - IPV)。由于生产条件要求(即高卫生标准、低脊髓灰质炎病毒感染强度和高人群免疫力),传统的索尔克IPV生产仅限于高收入工业化国家的制造商。在S - IPV生产中使用萨宾毒株具有较低的生物安全风险,并且被确定适合在发展中国家生产,这将扩大生产基地,并从长远来看使IPV更具可负担性和可及性。自2006年以来,S - IPV已取得重大进展。S - IPV目前在日本作为S - IPV获得许可,在中国作为独立的S - IPV获得许可,证明了这种疫苗的可行性。此外,生产工艺的改进可以进一步降低生产成本。后者对于这种疫苗在全球市场取得经济成功至关重要。我们总结了迄今为止S - IPV技术所取得的进展、支持S - IPV开发的科学数据和经济证据。

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