Hexon-chimaeric adenovirus serotype 5 vectors circumvent pre-existing anti-vector immunity

被引:0
|
作者
Diane M. Roberts
Anjali Nanda
Menzo J. E. Havenga
Peter Abbink
Diana M. Lynch
Bonnie A. Ewald
Jinyan Liu
Anna R. Thorner
Patricia E. Swanson
Darci A. Gorgone
Michelle A. Lifton
Angelique A. C. Lemckert
Lennart Holterman
Bing Chen
Athmanundh Dilraj
Angela Carville
Keith G. Mansfield
Jaap Goudsmit
Dan H. Barouch
机构
[1] Beth Israel Deaconess Medical Center,Division of Viral Pathogenesis
[2] Harvard Medical School,Laboratory of Molecular Medicine
[3] Crucell Holland BV,undefined
[4] Children's Hospital,undefined
[5] Harvard Medical School,undefined
[6] South African Medical Research Council,undefined
[7] New England Primate Research Center,undefined
来源
Nature | 2006年 / 441卷
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摘要
Adenovirus 5 (Ad5) causes mild respiratory tract infections in humans but its main claim to fame is as a potential vaccine vector for key diseases such as HIV/AIDS and malaria. Its potential clinical utility is, however, hampered by the fact that about half of the population in developed countries and 90% in Africa have been exposed to Ad5 before and have built up immunity. A team based at Harvard Medical School and the Dutch biotechnology company Crucell has devised a way of circumventing this problem by replacing parts of an Ad5 viral capsid protein with those from a related virus, the much rarer Ad48 adenovirus. The strategy was effective in tests in mice and monkeys; if the work can be repeated in humans then modified Ad5 will be a strong candidate as a vector for vaccines and also for delivering gene therapy.
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页码:239 / 243
页数:4
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