Long-term trial of protection provided by adenovirus-vectored vaccine expressing the PPRV H protein.

IF 6.9 1区 医学 Q1 IMMUNOLOGY
Karin E Darpel, Amanda Corla, Anna Stedman, Fiona Bellamy, John Flannery, Paulina Rajko-Nenow, Claire Powers, Steve Wilson, Bryan Charleston, Michael D Baron, Carrie Batten
{"title":"Long-term trial of protection provided by adenovirus-vectored vaccine expressing the PPRV H protein.","authors":"Karin E Darpel, Amanda Corla, Anna Stedman, Fiona Bellamy, John Flannery, Paulina Rajko-Nenow, Claire Powers, Steve Wilson, Bryan Charleston, Michael D Baron, Carrie Batten","doi":"10.1038/s41541-024-00892-2","DOIUrl":null,"url":null,"abstract":"<p><p>A recombinant, replication-defective, adenovirus-vectored vaccine expressing the H surface glycoprotein of peste des petits ruminants virus (PPRV) has previously been shown to protect goats from challenge with wild-type PPRV at up to 4 months post vaccination. Here, we present the results of a longer-term trial of the protection provided by such a vaccine, challenging animals at 6, 9, 12 and 15 months post vaccination. Vaccinated animals developed high levels of anti-PPRV H protein antibodies, which were virus-neutralising, and the level of these antibodies was maintained for the duration of the trial. The vaccinated animals were largely protected against overt clinical disease from the challenge virus. Although viral genome was intermittently detected in blood samples, nasal and/or ocular swabs of vaccinated goats post challenge, viral RNA levels were significantly lower compared to unvaccinated control animals and vaccinated goats did not appear to excrete live virus. This protection, like the antibody response, was maintained at the same level for at least 15 months after vaccination. In addition, we showed that animals that have been vaccinated with the adenovirus-based vaccine can be revaccinated with the same vaccine after 12 months and showed an increased anti-PPRV antibody response after this boost vaccination. Such vaccines, which provide a DIVA capability, would therefore be suitable for use when the current live attenuated PPRV vaccines are withdrawn at the end of the ongoing global PPR eradication campaign.</p>","PeriodicalId":19335,"journal":{"name":"NPJ Vaccines","volume":null,"pages":null},"PeriodicalIF":6.9000,"publicationDate":"2024-06-03","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11148195/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"NPJ Vaccines","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1038/s41541-024-00892-2","RegionNum":1,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"IMMUNOLOGY","Score":null,"Total":0}
引用次数: 0

Abstract

A recombinant, replication-defective, adenovirus-vectored vaccine expressing the H surface glycoprotein of peste des petits ruminants virus (PPRV) has previously been shown to protect goats from challenge with wild-type PPRV at up to 4 months post vaccination. Here, we present the results of a longer-term trial of the protection provided by such a vaccine, challenging animals at 6, 9, 12 and 15 months post vaccination. Vaccinated animals developed high levels of anti-PPRV H protein antibodies, which were virus-neutralising, and the level of these antibodies was maintained for the duration of the trial. The vaccinated animals were largely protected against overt clinical disease from the challenge virus. Although viral genome was intermittently detected in blood samples, nasal and/or ocular swabs of vaccinated goats post challenge, viral RNA levels were significantly lower compared to unvaccinated control animals and vaccinated goats did not appear to excrete live virus. This protection, like the antibody response, was maintained at the same level for at least 15 months after vaccination. In addition, we showed that animals that have been vaccinated with the adenovirus-based vaccine can be revaccinated with the same vaccine after 12 months and showed an increased anti-PPRV antibody response after this boost vaccination. Such vaccines, which provide a DIVA capability, would therefore be suitable for use when the current live attenuated PPRV vaccines are withdrawn at the end of the ongoing global PPR eradication campaign.

Abstract Image

表达 PPRV H 蛋白的腺病毒载体疫苗提供保护的长期试验。
一种表达小反刍兽疫病毒 (PPRV) H 表面糖蛋白的重组复制缺陷腺病毒载体疫苗曾被证明可保护山羊在接种后 4 个月内免受野生型 PPRV 的侵袭。在此,我们展示了对这种疫苗所提供的保护进行长期试验的结果,在接种后 6、9、12 和 15 个月对动物进行了挑战。接种疫苗的动物产生了高水平的抗PPRV H蛋白抗体,这种抗体具有病毒中和作用,并且在试验期间一直保持着这种抗体水平。接种疫苗的动物在很大程度上免受了挑战病毒引起的明显临床疾病的侵袭。虽然在接种疫苗后的山羊血液样本、鼻腔和/或眼部拭子中间歇性地检测到病毒基因组,但与未接种疫苗的对照组动物相比,病毒 RNA 水平明显较低,接种疫苗的山羊似乎没有排出活病毒。这种保护作用与抗体反应一样,在接种后至少 15 个月内保持在同一水平。此外,我们还发现,接种过腺病毒疫苗的动物可以在 12 个月后再次接种同样的疫苗,并且在接种这种加强免疫后显示出更强的抗 PPRV 抗体反应。这种疫苗具有 DIVA 功能,因此适合在当前的全球根除 PPRV 运动结束后,当前的 PPRV 减毒活疫苗退出市场时使用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
NPJ Vaccines
NPJ Vaccines Immunology and Microbiology-Immunology
CiteScore
11.90
自引率
4.30%
发文量
146
审稿时长
11 weeks
期刊介绍: Online-only and open access, npj Vaccines is dedicated to highlighting the most important scientific advances in vaccine research and development.
文献相关原料
公司名称 产品信息 采购帮参考价格
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信