Novel oral adjuvant to enhance cytotoxic memory like NK cell responses in HIV vaccine platform.

IF 6.9 1区 医学 Q1 IMMUNOLOGY NPJ Vaccines Pub Date : 2025-01-11 DOI:10.1038/s41541-024-01053-1
Mario Alles, Manuja Gunasena, Christina Isckarus, Ilmini De Silva, Sarah Board, Will Mulhern, Patrick L Collins, Thorsten Demberg, Namal P M Liyanage
{"title":"Novel oral adjuvant to enhance cytotoxic memory like NK cell responses in HIV vaccine platform.","authors":"Mario Alles, Manuja Gunasena, Christina Isckarus, Ilmini De Silva, Sarah Board, Will Mulhern, Patrick L Collins, Thorsten Demberg, Namal P M Liyanage","doi":"10.1038/s41541-024-01053-1","DOIUrl":null,"url":null,"abstract":"<p><p>Natural killer (NK) cell-driven effector mechanisms, such as antibody-dependent cell-mediated cytotoxicity, emerged as a secondary correlate of protection in the RV144 HIV vaccine clinical trial, the only vaccine thus far demonstrating some efficacy in human trials. Therefore, leveraging NK cells with enhanced cytotoxic effector responses may bolster vaccine-induced protection against HIV. Here, we investigated the effect of orally administering indole-3-carbinol (I3C), an aryl hydrocarbon receptor (AHR) agonist, as an adjuvant to an RV144-like vaccine platform in a mouse model. We demonstrate the expansion of KLRG1-expressing NK cells induced by the vaccine together with I3C. This NK cell subset exhibited enhanced vaccine antigen-specific cytotoxic memory-like features. Our study underscores the potential of incorporating I3C as an oral adjuvant to HIV vaccine platforms to enhance antigen-specific cytotoxicity of NK cells against HIV-infected cells. This approach may contribute to enhancing the protective efficacy of HIV preventive vaccines against HIV acquisition.</p>","PeriodicalId":19335,"journal":{"name":"NPJ Vaccines","volume":"10 1","pages":"5"},"PeriodicalIF":6.9000,"publicationDate":"2025-01-11","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11724931/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"NPJ Vaccines","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1038/s41541-024-01053-1","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

Natural killer (NK) cell-driven effector mechanisms, such as antibody-dependent cell-mediated cytotoxicity, emerged as a secondary correlate of protection in the RV144 HIV vaccine clinical trial, the only vaccine thus far demonstrating some efficacy in human trials. Therefore, leveraging NK cells with enhanced cytotoxic effector responses may bolster vaccine-induced protection against HIV. Here, we investigated the effect of orally administering indole-3-carbinol (I3C), an aryl hydrocarbon receptor (AHR) agonist, as an adjuvant to an RV144-like vaccine platform in a mouse model. We demonstrate the expansion of KLRG1-expressing NK cells induced by the vaccine together with I3C. This NK cell subset exhibited enhanced vaccine antigen-specific cytotoxic memory-like features. Our study underscores the potential of incorporating I3C as an oral adjuvant to HIV vaccine platforms to enhance antigen-specific cytotoxicity of NK cells against HIV-infected cells. This approach may contribute to enhancing the protective efficacy of HIV preventive vaccines against HIV acquisition.

查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
新型口服佐剂增强细胞毒性记忆,如NK细胞在HIV疫苗平台上的反应。
自然杀伤(NK)细胞驱动的效应机制,如抗体依赖细胞介导的细胞毒性,在RV144 HIV疫苗临床试验中作为保护的次要相关因素出现,RV144疫苗是迄今为止唯一在人体试验中显示出一定功效的疫苗。因此,利用具有增强细胞毒性效应反应的NK细胞可能增强疫苗诱导的对HIV的保护。在此,我们在小鼠模型中研究了口服芳基烃受体(AHR)激动剂吲哚-3-甲醇(I3C)作为rv144样疫苗平台的佐剂的效果。我们证实了该疫苗与I3C共同诱导表达klrg1的NK细胞扩增。NK细胞亚群表现出增强的疫苗抗原特异性细胞毒性记忆样特征。我们的研究强调了将I3C作为HIV疫苗平台的口服佐剂来增强NK细胞对HIV感染细胞的抗原特异性细胞毒性的潜力。这种方法可能有助于提高艾滋病毒预防疫苗对艾滋病毒感染的保护功效。
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 去求助
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.
期刊最新文献
Recombinant production platform for Group A Streptococcus glycoconjugate vaccines. Saponin-based adjuvant uptake and induction of antigen cross-presentation by CD11b+ dendritic cells and macrophages. Validation of a multiplexed immunoassay for immunological analysis of pre erythrocytic malaria vaccines. TLR7/8/9 agonists and low-dose cisplatin synergistically promotes tertiary lymphatic structure formation and antitumor immunity. HLA I immunopeptidome of synthetic long peptide pulsed human dendritic cells for therapeutic vaccine design.
×
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
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 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 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1