A MVA construct expressing a secretable form of the Dengue virus 3 envelope protein protects immunized mice from dengue-induced encephalitis

•MVA expressing a DENV protein directed to the ER induces neutralizing antibodies.•Vaccination with MVA expressing a secretable E protein abrogates encephalitis in mice.•MVA expressing a non-secretable E protein does not protect mice from encephalitis. Dengue is no longer restricted to tropical deve...

Full description

Saved in:
Bibliographic Details
Published inVaccine Vol. 34; no. 50; pp. 6120 - 6122
Main Authors Quinan, Bárbara R., Versiani, Alice Freitas, da Fonseca, Flávio G.
Format Journal Article
LanguageEnglish
Published Netherlands Elsevier Ltd 07.12.2016
Elsevier Limited
Subjects
Online AccessGet full text
ISSN0264-410X
1873-2518
1873-2518
DOI10.1016/j.vaccine.2016.10.058

Cover

Loading…
More Information
Summary:•MVA expressing a DENV protein directed to the ER induces neutralizing antibodies.•Vaccination with MVA expressing a secretable E protein abrogates encephalitis in mice.•MVA expressing a non-secretable E protein does not protect mice from encephalitis. Dengue is no longer restricted to tropical developing countries, but is now a major global public health problem. Despite the recent license approval of the CYD-TDV vaccine in some countries, efforts to develop a more efficient vaccine against Dengue virus (DENV) continue. Herein, we evaluate the immunogenicity and level of protection of two potential vaccines against DENV based on recombinant modified vaccinia virus Ankara (rMVA). The vaccine addressing the Envelope protein from DENV serotype 3 to the endoplasmic reticulum elicited neutralizing antibodies titers which correlate with protection, and also confers protection upon challenge in a mouse model. Our results support the development of a tetravalent dengue vaccine with the further construction of rMVAs expressing proteins from the other DENV serotypes.
Bibliography:ObjectType-Article-1
SourceType-Scholarly Journals-1
ObjectType-Feature-2
content type line 14
content type line 23
ISSN:0264-410X
1873-2518
1873-2518
DOI:10.1016/j.vaccine.2016.10.058