免疫系统
免疫学
呼吸系统
肺
医学
炎症
呼吸道疾病
受体
基因传递
生物
全身炎症
载体(分子生物学)
呼吸道
平衡
细胞因子
作者
Ntombizodwa Makuyana,Laura Seldeslachts,Lauren Michiels,Oliver T. Burton,Alvaro R. Hernandez,Arman Ghodsinia,Ekhlas Rahman,Laura M. Kops,K. N. Singh,Fran Naranjo,Magda Ali,Amy Dashwood,Marwane Achkir,Lubna Kouser,Stéphanie Liénart,Stéphane Guillaume,Lieve Naesens,Michelle A. Linterman,Joost Wauters,Régis Joulia
出处
期刊:Science immunology
[American Association for the Advancement of Science]
日期:2026-04-17
卷期号:11 (118): eadv7969-eadv7969
标识
DOI:10.1126/sciimmunol.adv7969
摘要
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.
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