Gene delivery of immunomodulatory cytokines to the lung preserves respiratory function during inflammatory challenge

IF 16.4 1区 医学 Q1 IMMUNOLOGY
Ntombizodwa Makuyana, Laura Seldeslachts, Lauren Michiels, Oliver T. Burton, Alvaro R. Hernandez, Arman Ghodsinia, Ekhlas Rahman, Laura M. Kops, Kailash Singh, Fran Naranjo, Magda Ali, Amy Dashwood, Marwane Achkir, Lubna Kouser, Stephanie Lienart, Stephane Guillaume, Lieve Naesens, Michelle A. Linterman, Joost Wauters, Régis Joulia, Stephanie Humblet-Baron, Greetje Vande Velde, James Dooley, Adrian Liston
{"title":"Gene delivery of immunomodulatory cytokines to the lung preserves respiratory function during inflammatory challenge","authors":"Ntombizodwa Makuyana,&nbsp;Laura Seldeslachts,&nbsp;Lauren Michiels,&nbsp;Oliver T. Burton,&nbsp;Alvaro R. Hernandez,&nbsp;Arman Ghodsinia,&nbsp;Ekhlas Rahman,&nbsp;Laura M. Kops,&nbsp;Kailash Singh,&nbsp;Fran Naranjo,&nbsp;Magda Ali,&nbsp;Amy Dashwood,&nbsp;Marwane Achkir,&nbsp;Lubna Kouser,&nbsp;Stephanie Lienart,&nbsp;Stephane Guillaume,&nbsp;Lieve Naesens,&nbsp;Michelle A. Linterman,&nbsp;Joost Wauters,&nbsp;Régis Joulia,&nbsp;Stephanie Humblet-Baron,&nbsp;Greetje Vande Velde,&nbsp;James Dooley,&nbsp;Adrian Liston","doi":"10.1126/sciimmunol.adv7969","DOIUrl":null,"url":null,"abstract":"<div >Respiratory infections that result in severe and life-threatening immune-mediated respiratory decline are a major public health issue. Controlling local respiratory immune reactions without the use of systemic immunosuppressants remains an unmet clinical challenge. We developed a gene delivery system to express anti-inflammatory cytokines in the lung, which reestablishes local immune homeostasis without triggering systemic effects. Using an adeno-associated vector cargo system (AAV6.2-<i>CC10</i>), we induced production of interleukin-2 (IL-2), IL-1 receptor antagonist (IL-1RA), and IL-10 in situ in the lung microenvironment, with no detectable expression or immunological deviation in the peripheral immune system. We demonstrate the effective potential of IL-2, IL-1RA, and IL-10 as immunomodulatory cargos in severe infectious challenge, which reduced respiratory pathology after influenza-associated pulmonary aspergillosis. Thus, the AAV6.2-<i>CC10</i> platform enables targeted delivery of biologics to the lung, modulates the lung environment, and improves pathology without inducing systemic immune reactions.</div>","PeriodicalId":21734,"journal":{"name":"Science Immunology","volume":"11 118","pages":""},"PeriodicalIF":16.4000,"publicationDate":"2026-04-17","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Science Immunology","FirstCategoryId":"3","ListUrlMain":"https://www.science.org/doi/10.1126/sciimmunol.adv7969","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

Respiratory infections that result in severe and life-threatening immune-mediated respiratory decline are a major public health issue. Controlling local respiratory immune reactions without the use of systemic immunosuppressants remains an unmet clinical challenge. We developed a gene delivery system to express anti-inflammatory cytokines in the lung, which reestablishes local immune homeostasis without triggering systemic effects. Using an adeno-associated vector cargo system (AAV6.2-CC10), we induced production of interleukin-2 (IL-2), IL-1 receptor antagonist (IL-1RA), and IL-10 in situ in the lung microenvironment, with no detectable expression or immunological deviation in the peripheral immune system. We demonstrate the effective potential of IL-2, IL-1RA, and IL-10 as immunomodulatory cargos in severe infectious challenge, which reduced respiratory pathology after influenza-associated pulmonary aspergillosis. Thus, the AAV6.2-CC10 platform enables targeted delivery of biologics to the lung, modulates the lung environment, and improves pathology without inducing systemic immune reactions.
免疫调节细胞因子的基因传递到肺在炎症挑战期间保持呼吸功能
导致严重和危及生命的免疫介导的呼吸衰退的呼吸道感染是一个重大的公共卫生问题。在不使用全身免疫抑制剂的情况下控制局部呼吸免疫反应仍然是一个尚未实现的临床挑战。我们开发了一种基因传递系统来表达肺中的抗炎细胞因子,从而在不触发全身效应的情况下重建局部免疫稳态。利用腺相关载体载体系统(AAV6.2- CC10),我们在肺微环境中原位诱导了白细胞介素-2 (IL-2)、IL-1受体拮抗剂(IL-1RA)和IL-10的产生,在外周免疫系统中没有检测到表达或免疫偏差。我们证明了IL-2、IL-1RA和IL-10在严重感染挑战中作为免疫调节货物的有效潜力,这减少了流感相关肺曲霉病后的呼吸道病理。因此,AAV6.2- CC10平台可以在不诱导全身免疫反应的情况下,将生物制剂靶向递送到肺部,调节肺部环境,改善病理。
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
Science Immunology
Science Immunology Immunology and Microbiology-Immunology
CiteScore
32.90
自引率
2.00%
发文量
183
期刊介绍: Science Immunology is a peer-reviewed journal that publishes original research articles in the field of immunology. The journal encourages the submission of research findings from all areas of immunology, including studies on innate and adaptive immunity, immune cell development and differentiation, immunogenomics, systems immunology, structural immunology, antigen presentation, immunometabolism, and mucosal immunology. Additionally, the journal covers research on immune contributions to health and disease, such as host defense, inflammation, cancer immunology, autoimmunity, allergy, transplantation, and immunodeficiency. Science Immunology maintains the same high-quality standard as other journals in the Science family and aims to facilitate understanding of the immune system by showcasing innovative advances in immunology research from all organisms and model systems, including humans.
×
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