Sutter Roland W, Eisenhawer Martin, Molodecky Natalia A, Verma Harish, Okayasu Hiromasa
Tamayo Federal Solutions LLC, Virginia Beach, VA 23452, USA.
Polio Eradication Department, World Health Organization, 1211 Geneva, Switzerland.
Pathogens. 2024 Mar 4;13(3):224. doi: 10.3390/pathogens13030224.
Inactivated poliovirus vaccine (IPV), available since 1955, became the first vaccine to be used to protect against poliomyelitis. While the immunogenicity of IPV to prevent paralytic poliomyelitis continues to be irrefutable, its requirement for strong containment (due to large quantities of live virus used in the manufacturing process), perceived lack of ability to induce intestinal mucosal immunity, high cost and increased complexity to administer compared to oral polio vaccine (OPV), have limited its use in the global efforts to eradicate poliomyelitis. In order to harvest the full potential of IPV, a program of work has been carried out by the Global Polio Eradication Initiative (GPEI) over the past two decades that has focused on: (1) increasing the scientific knowledge base of IPV; (2) translating new insights and evidence into programmatic action; (3) expanding the IPV manufacturing infrastructure for global demand; and (4) continuing to pursue an ambitious research program to develop more immunogenic and safer-to-produce vaccines. While the knowledge base of IPV continues to expand, further research and product development are necessary to ensure that the program priorities are met (e.g., non-infectious production through virus-like particles, non-transmissible vaccine inducing humoral and intestinal mucosal immunity and new methods for house-to-house administration through micro-needle patches and jet injectors), the discussions have largely moved from whether to how to use this vaccine most effectively. In this review, we summarize recent developments on expanding the science base of IPV and provide insight into policy development and the expansion of IPV manufacturing and production, and finally we provide an update on the current priorities.
灭活脊髓灰质炎病毒疫苗(IPV)自1955年问世以来,成为首个用于预防脊髓灰质炎的疫苗。尽管IPV预防麻痹型脊髓灰质炎的免疫原性无可争议,但其对严格管控的要求(由于生产过程中使用大量活病毒)、被认为缺乏诱导肠道黏膜免疫的能力、成本高昂以及与口服脊髓灰质炎疫苗(OPV)相比接种复杂性增加,限制了其在全球根除脊髓灰质炎努力中的应用。为充分发挥IPV的潜力,全球根除脊髓灰质炎行动(GPEI)在过去二十年开展了一项工作方案,重点关注:(1)增加IPV的科学知识基础;(2)将新见解和证据转化为规划行动;(3)扩大IPV生产基础设施以满足全球需求;(4)继续推行一项雄心勃勃的研究计划,以开发免疫原性更强且生产更安全的疫苗。虽然IPV的知识基础不断扩大,但仍需进一步研究和产品开发,以确保实现方案优先事项(例如通过病毒样颗粒进行非感染性生产、诱导体液和肠道黏膜免疫的非传播性疫苗以及通过微针贴片和喷射注射器进行逐户接种的新方法),讨论已基本从是否使用该疫苗转向如何最有效地使用它。在本综述中,我们总结了扩大IPV科学基础的近期进展,并深入探讨政策制定以及IPV制造和生产的扩展,最后提供当前优先事项的最新情况。