Yellow fever 17D-vectored vaccines expressing Lassa virus GP1 and GP2 glycoproteins provide protection against fatal disease in guinea pigs

Yellow Fever (YF) and Lassa Fever (LF) are two prevalent hemorrhagic fevers co-circulating in West Africa and responsible for thousands of deaths annually. The YF vaccine 17D has been used as a vector for the Lassa virus glycoprotein precursor (LASV-GPC) or their subunits, GP1 (attachment glycoprote...

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Published inVaccine Vol. 29; no. 6; pp. 1248 - 1257
Main Authors Jiang, Xiaohong, Dalebout, Tim J, Bredenbeek, Peter J, Carrion, Ricardo, Brasky, Kathleen, Patterson, Jean, Goicochea, Marco, Bryant, Joseph, Salvato, Maria S, Lukashevich, Igor S
Format Journal Article
LanguageEnglish
Published Kidlington Elsevier Ltd 01.02.2011
Elsevier
Elsevier Limited
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Summary:Yellow Fever (YF) and Lassa Fever (LF) are two prevalent hemorrhagic fevers co-circulating in West Africa and responsible for thousands of deaths annually. The YF vaccine 17D has been used as a vector for the Lassa virus glycoprotein precursor (LASV-GPC) or their subunits, GP1 (attachment glycoprotein) and GP2 (fusion glycoprotein). Cloning shorter inserts, LASV-GP1 and -GP2, between YF17D E and NS1 genes enhanced genetic stability of recombinant viruses, YF17D/LASV-GP1 and -GP2, in comparison with YF17D/LASV-GPC recombinant. The recombinant viruses were replication competent and properly processed YF proteins and LASV GP antigens in infected cells. YF17D/LASV-GP1 and -GP2 induced specific CD8+ T cell responses in mice and protected strain 13 guinea pigs against fatal LF. Unlike immunization with live attenuated reassortant vaccine ML29, immunization with YF17D/LASV-GP1 and -GP2 did not provide sterilizing immunity. This study demonstrates the feasibility of YF17D-based vaccine to control LF in West Africa.
Bibliography:http://dx.doi.org/10.1016/j.vaccine.2010.11.079
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ISSN:0264-410X
1873-2518
DOI:10.1016/j.vaccine.2010.11.079