Boyer Julie L, Kobinger Gary, Wilson James M, Crystal Ronald G
Department of Genetic Medicine, Weill Medical College of Cornell University, New York, NY 10021, USA.
Hum Gene Ther. 2005 Feb;16(2):157-68. doi: 10.1089/hum.2005.16.157.
The robust host responses elicited against transgenes encoded by (E1-)(E3-) adenovirus (Ad) gene transfer vectors can be used to develop Ad-based vectors as platform technologies for vaccines against potential bioterror pathogens. This review focuses on pathogens of major concern as bioterror agents and why Ad vectors are ideal as anti-bioterror vaccine platforms, providing examples from our laboratories of using Ad vectors as vaccines against potential bioterror pathogens and how Ad vectors can be developed to enhance vaccine efficacy in the bioterror war.
针对(E1-)(E3-)腺病毒(Ad)基因转移载体所编码转基因引发的强大宿主反应,可用于开发基于Ad的载体,作为针对潜在生物恐怖病原体的疫苗平台技术。本综述聚焦于作为生物恐怖剂备受关注的病原体,以及为何Ad载体是理想的抗生物恐怖疫苗平台,并列举我们实验室利用Ad载体作为针对潜在生物恐怖病原体疫苗的实例,以及在生物恐怖战争中如何开发Ad载体以提高疫苗效力。