Theoretical Biology and Biophysics, MS K710, Los Alamos National Laboratory, Los Alamos, NM 87545, USA.
Center for Global Health, MSC10 5550, Division of Infectious Diseases, Department of Internal Medicine, University of New Mexico, Albuquerque, NM 87131, USA.
Vaccine. 2018 Nov 12;36(46):6911-6917. doi: 10.1016/j.vaccine.2018.10.022. Epub 2018 Oct 15.
Zika virus (ZIKV) is a mosquito-borne flavivirus that was first discovered in 1947. Since then, outbreaks have been reported in tropical Africa, Southeast Asia, the Pacific Islands, and, in 2015, in the Americas. Since 2013, many countries have reported cases of microcephaly and other central nervous system malformation associated with ZIKV. Because the initial target population for a ZIKV vaccine is expected to be women of child-bearing age, including those who may be pregnant, it is necessary to develop safe, easily administered, and non-viral vaccines. Here, we show that a single tetrafunctional Amphiphilic Block Copolymer (ABC) delivers DNA that encodes the full natural sequence of prM-E, among other antigen designs tested, induces the highest antibody titer and neutralization activity against three divergent ZIKV isolates. Vaccination with a single tetrafunctional block copolymer delivering low dose (10 µg) DNA plasmid rapidly induces protection from detectable viremia during acute infection in mice challenged by ZIKV more than 7 months after their first vaccination and boosted 2 weeks before challenge. This use of tetrafunctional ABCs is a new approach to deliver DNA antigens against flaviviruses. The data demonstrate that DNA formulated by a tetrafunctional block copolymer rapidly elicits protective responses against multiple diverse ZIKV isolates. This represents potential for an easy-to-administer and simple to manufacture vaccine candidate against ZIKV and possibly other emerging threats to global health.
寨卡病毒(ZIKV)是一种蚊媒黄病毒,于 1947 年首次发现。自那时以来,寨卡病毒已在热带非洲、东南亚、太平洋岛屿爆发,并于 2015 年在美洲爆发。自 2013 年以来,许多国家报告了与寨卡病毒相关的小头症和其他中枢神经系统畸形病例。由于预计寨卡病毒疫苗的初始目标人群是育龄妇女,包括可能怀孕的妇女,因此有必要开发安全、易于管理和非病毒疫苗。在这里,我们展示了一种单价四功能两亲嵌段共聚物(ABC)可传递 DNA,该 DNA 编码 prM-E 的全长天然序列,以及其他经过测试的抗原设计,可诱导针对三种不同 ZIKV 分离株的最高抗体滴度和中和活性。单次接种单价四功能嵌段共聚物递送低剂量(10μg)DNA 质粒可迅速诱导保护,使其免受急性感染期间的可检测病毒血症的影响,在首次接种后 7 个月以上和挑战前 2 周加强后,用 ZIKV 攻击的小鼠中。这种使用单价四功能 ABC 的方法是一种新的方法,可用于传递针对黄病毒的 DNA 抗原。数据表明,单价四功能嵌段共聚物配方可迅速引发针对多种不同 ZIKV 分离株的保护性反应。这代表了针对寨卡病毒和可能对全球健康构成的其他新威胁的易于管理和简单制造疫苗候选物的潜力。