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口蹄疫病毒疫苗

Foot and mouth disease virus vaccines.

作者信息

Rodriguez Luis L, Grubman Marvin J

机构信息

Foreign Animal Disease Research Unit, Agricultural Research Service, U.S. Department of Agriculture, Plum Island Animal Disease Center, Greenport, NY 11944-0848, USA.

出版信息

Vaccine. 2009 Nov 5;27 Suppl 4:D90-4. doi: 10.1016/j.vaccine.2009.08.039.

Abstract

Foot and mouth disease (FMD) is a highly infectious and economically devastating disease of livestock. Although vaccines, available since the early 1900s, have been instrumental in eradicating FMD from parts of the world, the disease still affects millions of animals around the globe and remains the main sanitary barrier to the commerce of animals and animal products. Currently available inactivated antigen vaccines applied intramuscularly to individual animals, confer serotype and subtype specific protection in 1-2 weeks but fail to induce long-term protective immunity. Among the limitations of this vaccine are potential virus escape from the production facility, short shelf life of formulated product, short duration of immunity and requirement of dozens of antigens to address viral antigenic diversity. Here we review novel vaccine approaches that address some of these limitations. Basic research and the combination of reliable animal inoculation models, reverse genetics and computational biology tools will allow the rational design of safe and effective FMD vaccines. These vaccines should address not only the needs of FMD-free countries but also allow the progressive global control and eradication of this devastating disease.

摘要

口蹄疫(FMD)是一种对家畜具有高度传染性且造成巨大经济损失的疾病。尽管自20世纪初就有疫苗问世,这些疫苗在世界部分地区根除口蹄疫方面发挥了重要作用,但该疾病仍影响着全球数百万头动物,并且仍然是动物及动物产品贸易的主要卫生障碍。目前可用的灭活抗原疫苗通过肌肉注射给个体动物,可在1至2周内提供血清型和亚型特异性保护,但无法诱导长期保护性免疫。这种疫苗的局限性包括生产设施中可能出现病毒逃逸、配制产品的保质期短、免疫持续时间短以及需要数十种抗原以应对病毒的抗原多样性。在此,我们综述了一些可解决其中部分局限性的新型疫苗方法。基础研究以及可靠的动物接种模型、反向遗传学和计算生物学工具的结合,将有助于合理设计安全有效的口蹄疫疫苗。这些疫苗不仅应满足无口蹄疫国家的需求,还应有助于逐步在全球范围内控制和根除这种毁灭性疾病。

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