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Establishing a Robust Manufacturing Platform for Recombinant Veterinary Vaccines: An Adenovirus-Vector Vaccine to Control Newcastle Disease Virus Infections of Poultry in Sub-Saharan Africa

机译:建立强大的重组疫苗生产平台:控制撒哈拉以南非洲地区家禽新城疫病毒感染的腺病毒载体疫苗

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摘要

Developing vaccine technology platforms to respond to pandemic threats or zoonotic diseases is a worldwide high priority. The risk of infectious diseases transmitted from wildlife and domestic animals to humans makes veterinary vaccination and animal health monitoring highly relevant for the deployment of public health global policies in the context of “one world, one health” principles. Sub-Saharan Africa is frequently impacted by outbreaks of poultry diseases such as avian influenza and Newcastle Disease (ND). Here, an adenovirus-vectored vaccine technology platform is proposed for rapid adaptation to ND or other avian viral threats in the region. Ethiopian isolates of the Newcastle Disease virus (NDV) were subjected to sequence and phylogenetic analyses, enabling the construction of antigenically matched vaccine candidates expressing the fusion (F) and hemagglutinin-neuraminidase (HN) proteins. A cost-effective vaccine production process was developed using HEK293 cells in suspension and serum-free medium. Productive infection in bioreactors (1–3 L) at 2 × 10 cells/mL resulted in consistent infectious adenoviral vector titers of approximately 5–6 × 10 TCID /mL (approximately 10 VP/mL) in the harvest lysates. Groups of chickens were twice immunized with 1 × 10 TCID of the vectors, and full protection against a lethal NDV challenge was provided by the vector expressing the F antigen. These results consolidate the basis for a streamlined and scalable-vectored vaccine manufacturing process for deployment in low- and medium-income countries.
机译:开发疫苗技术平台以应对大流行性威胁或人畜共患疾病是全球高度优先的工作。从野生动植物和家畜传播给人类的传染病风险使兽医接种和动物健康监测与在“一个世界,一个健康”原则范围内部署公共卫生全球政策高度相关。撒哈拉以南非洲地区经常受到禽流感和新城疫等家禽疾病暴发的影响。在此,提出了一种腺病毒载体疫苗技术平台,用于快速适应该地区的ND或其他禽病毒威胁。对新城疫病毒(NDV)的埃塞俄比亚分离株进行了序列和系统发育分析,从而能够构建表达融合蛋白(F)和血凝素神经氨酸酶(HN)蛋白的抗原匹配疫苗候选物。在悬浮液和无血清培养基中使用HEK293细胞开发了一种经济有效的疫苗生产方法。在生物反应器(1-3 L)中以2×10个细胞/ mL进行有效感染,在收获的裂解物中产生一致的传染性腺病毒载体滴度,约为5-6×10 TCID / mL(约10 VP / mL)。用1×10 TCID的载体对两组鸡进行两次免疫,表达F抗原的载体可提供对致命NDV攻击的全面保护。这些结果为简化和可扩展的矢量化疫苗生产过程的基础奠定了基础,以便在中低收入国家中进行部署。

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