Marburg virus vaccines: comparing classical and new approaches

被引:51
作者
Hevey, M [1 ]
Negley, D [1 ]
VanderZanden, L [1 ]
Tammariello, RF [1 ]
Geisbert, J [1 ]
Schmaljohn, C [1 ]
Smith, JF [1 ]
Jahrling, PB [1 ]
Schmaljohn, AL [1 ]
机构
[1] USA, Med Res Inst Infect Dis, Div Virol, Frederick, MD 21702 USA
关键词
Marburg virus; vaccine; guinea pie;
D O I
10.1016/S0264-410X(01)00353-X
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
An effort to develop a safe and effective vaccine for Marburg virus (MBGV), one of the filoviruses known to cause high mortality rates in humans, led us to compare directly some of the merits of modem versus classical vaccine approaches for this agent. Prior work had established the MBGV-glycoprotein (GP), the only known virion surface antigen, as a candidate for inclusion in a vaccine. In this study we vaccinated groups of Hartley guinea pigs with killed MBGV, live attenuated MBGV. soluble MBGV-GP expressed by baculovirus recombinants, MBGV-GP delivered as a DNA vaccine. or MBGV-GP delivered via an alphavirus RNA replicon. Serological responses were evaluated. and animals were challenged with a lethal dose of MBGV given either subcutaneously or via aerosol. Killed MBGV and replicon-delivered MBGV-GP were notably immunogenic and protective against MBGV, but results did not exclude any approach and suggested a role for DNA vaccines in immunological priming. (C) 2001 Published by Elsevier Science Ltd.
引用
收藏
页码:586 / 593
页数:8
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