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(Reference retrieved automatically from Web of Science through information on FAPESP grant and its corresponding number as mentioned in the publication by the authors.)

Protective efficacy of multiple vaccine platforms against Zika virus challenge in rhesus monkeys

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Author(s):
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Abbink, Peter ; Larocca, Rafael A. ; De La Barrera, Rafael A. ; Bricault, Christine A. ; Moseley, Edward T. ; Boyd, Michael ; Kirilova, Marinela ; Li, Zhenfeng ; Ng'ang'a, David ; Nanayakkara, Ovini ; Nityanandam, Ramya ; Mercado, Noe B. ; Borducchi, Erica N. ; Agarwal, Arshi ; Brinkman, Amanda L. ; Cabral, Crystal ; Chandrashekar, Abishek ; Giglio, Patricia B. ; Jetton, David ; Jimenez, Jessica ; Lee, Benjamin C. ; Mojta, Shanell ; Molloy, Katherine ; Shetty, Mayuri ; Neubauer, George H. ; Stephenson, Kathryn E. ; Peron, Jean Pierre S. ; Zanotto, Paolo M. de A. ; Misamore, Johnathan ; Finneyfrock, Brad ; Lewis, Mark G. ; Alter, Galit ; Modjarrad, Kayvon ; Jarman, Richard G. ; Eckels, Kenneth H. ; Michael, Nelson L. ; Thomas, Stephen J. ; Barouch, Dan H.
Total Authors: 38
Document type: Journal article
Source: Science; v. 353, n. 6304, p. 1129-1132, SEP 9 2016.
Web of Science Citations: 227
Abstract

Zika virus (ZIKV) is responsible for a major ongoing epidemic in the Americas and has been causally associated with fetal microcephaly. The development of a safe and effective ZIKV vaccine is therefore an urgent global health priority. Here we demonstrate that three different vaccine platforms protect against ZIKV challenge in rhesus monkeys. A purified inactivated virus vaccine induced ZIKV-specific neutralizing antibodies and completely protected monkeys against ZIKV strains from both Brazil and Puerto Rico. Purified immunoglobulin from vaccinated monkeys also conferred passive protection in adoptive transfer studies. A plasmid DNA vaccine and a single-shot recombinant rhesus adenovirus serotype 52 vector vaccine, both expressing ZIKV premembrane and envelope, also elicited neutralizing antibodies and completely protected monkeys against ZIKV challenge. These data support the rapid clinical development of ZIKV vaccines for humans. (AU)

FAPESP's process: 14/17766-9 - A systemic approach to study permissivity on the Anticarsia gemmatalis multiple nucleopolyhedrovirus (AgMNPV)
Grantee:Paolo Marinho de Andrade Zanotto
Support Opportunities: Regular Research Grants
FAPESP's process: 11/18703-2 - The role of Indoleamine-2,3-dioxigenase and the Triptophan - Kynurenines axis through NMDA receptors over the immune response in the EAE and stroke model
Grantee:Jean Pierre Schatzmann Peron
Support Opportunities: Research Grants - Young Investigators Grants