寨卡病毒
病毒学
抗体
中和抗体
血清型
小头畸形
生物
病毒
dna疫苗
免疫
医学
免疫学
遗传学
作者
Peter Abbink,Rafael A. Larocca,Rafael A. De La Barrera,Christine A. Bricault,Edward T. Moseley,Michael Boyd,Marinela Kirilova,Zhenfeng Li,David Ng’ang’a,Ovini Nanayakkara,Ramya Nityanandam,Noe B. Mercado,Erica N. Borducchi,Arshi Agarwal,Amanda Brinkman,Crystal Cabral,Abishek Chandrashekar,Patricia Giglio,David Jetton,Jessica Jimenez
出处
期刊:Science
[American Association for the Advancement of Science]
日期:2016-08-04
卷期号:353 (6304): 1129-1132
被引量:510
标识
DOI:10.1126/science.aah6157
摘要
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.
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