Safety and immunogenicity testing of a melioidosis subunit vaccine candidate in cynomolgus macaques.

IF 7.2 1区 医学 Q1 IMMUNOLOGY
Sineenart Sengyee, Caitlyn E Orne, Sarah B Weiby, Lindsey K Schmidt, Federico Urbano-Munoz, Jiri Vlach, Christian Heiss, Parastoo Azadi, Narisara Chantratita, Mary N Burtnick, Paul J Brett
{"title":"Safety and immunogenicity testing of a melioidosis subunit vaccine candidate in cynomolgus macaques.","authors":"Sineenart Sengyee, Caitlyn E Orne, Sarah B Weiby, Lindsey K Schmidt, Federico Urbano-Munoz, Jiri Vlach, Christian Heiss, Parastoo Azadi, Narisara Chantratita, Mary N Burtnick, Paul J Brett","doi":"10.1038/s41541-026-01526-5","DOIUrl":null,"url":null,"abstract":"<p><p>Burkholderia pseudomallei, the etiologic agent of melioidosis, is a Gram-negative bacterial pathogen that causes severe disease in humans and animals. In this study, we evaluated the safety and immunogenicity of our lead melioidosis subunit vaccine candidate in cynomolgus macaques. To accomplish this, the 6-deoxyheptan capsular polysaccharide (CPS) from Burkholderia thailandensis E555 was purified using a phenol-free extraction process and then conjugated to CRM197 to generate CPS-CRM197. Highly purified, His-tagless B. pseudomallei Hcp1 (Hcp1-TL) was also produced. Animals immunized with CPS-CRM197 combined with Hcp1-TL and adjuvanted with Alhydrogel plus CpG DNA (ODN 2006) developed robust CPS-specific IgG and opsonizing antibody responses, alongside strong Hcp1-specific IgG and measurable IFN-γ-secreting T-cell responses. Importantly, the vaccine formulations tested were well tolerated, with no adverse events after three doses. Collectively, these studies establish good manufacturing practices-compatible processes for our vaccine antigens and demonstrate the safety and immunogenicity of the subunit vaccine in non-human primates, supporting continued advancement towards a human clinical trial.</p>","PeriodicalId":19335,"journal":{"name":"NPJ Vaccines","volume":" ","pages":""},"PeriodicalIF":7.2000,"publicationDate":"2026-07-14","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"NPJ Vaccines","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1038/s41541-026-01526-5","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

Burkholderia pseudomallei, the etiologic agent of melioidosis, is a Gram-negative bacterial pathogen that causes severe disease in humans and animals. In this study, we evaluated the safety and immunogenicity of our lead melioidosis subunit vaccine candidate in cynomolgus macaques. To accomplish this, the 6-deoxyheptan capsular polysaccharide (CPS) from Burkholderia thailandensis E555 was purified using a phenol-free extraction process and then conjugated to CRM197 to generate CPS-CRM197. Highly purified, His-tagless B. pseudomallei Hcp1 (Hcp1-TL) was also produced. Animals immunized with CPS-CRM197 combined with Hcp1-TL and adjuvanted with Alhydrogel plus CpG DNA (ODN 2006) developed robust CPS-specific IgG and opsonizing antibody responses, alongside strong Hcp1-specific IgG and measurable IFN-γ-secreting T-cell responses. Importantly, the vaccine formulations tested were well tolerated, with no adverse events after three doses. Collectively, these studies establish good manufacturing practices-compatible processes for our vaccine antigens and demonstrate the safety and immunogenicity of the subunit vaccine in non-human primates, supporting continued advancement towards a human clinical trial.

食蟹猴类鼻疽亚单位候选疫苗的安全性和免疫原性试验。
伪伯克霍尔德菌是类鼻疽病的病原,是一种革兰氏阴性细菌病原体,可引起人类和动物的严重疾病。在这项研究中,我们在食蟹猴中评估了我们的类鼻疽铅亚单位候选疫苗的安全性和免疫原性。为了实现这一目标,采用无酚提取工艺纯化泰国伯克霍尔德菌E555中的6-脱氧庚烷荚膜多糖(CPS),然后与CRM197偶联生成CPS-CRM197。高纯度的无His-tagless pseudomallei Hcp1 (Hcp1- tl)也得到了。用CPS-CRM197联合Hcp1-TL免疫动物,并用Alhydrogel + CpG DNA佐剂(ODN 2006)免疫动物,产生了强大的cps特异性IgG和活化抗体反应,以及强大的hcp1特异性IgG和可测量的IFN-γ分泌t细胞反应。重要的是,测试的疫苗制剂耐受性良好,三次剂量后没有出现不良事件。总的来说,这些研究为我们的疫苗抗原建立了符合良好生产规范的流程,并证明了亚单位疫苗在非人灵长类动物中的安全性和免疫原性,支持继续推进人体临床试验。
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.
×
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:604180095
Book学术官方微信
小红书