医学
慢性阻塞性肺病
粘液
免疫学
恶化
趋化因子
炎症
病毒
免疫系统
CXCL11型
甲型流感病毒
肺
肺病
分泌物
发病机制
病毒学
单反病毒
免疫病理学
呼吸系统
呼吸道
呼吸上皮
白细胞介素8
CXCL10型
疾病
抗体
作者
M. Camila Melo-Narváez,Christian Eger,Wilhelm Bertrams,Birke J. Benedikter,Feng Ling,Matthew R. Jones,Anna Lena Jung,Kim Pauck,Barbara Weckler,Hendrik Pott,Tara Procida-Kowalski,Jochen Wilhelm,Evelyn Vollmeister,Holger Garn,Andreas Kirschbaum,Gernot Rohde,Małgorzata Wygrecka,Janna Nawroth,Carlos Talavera‐López,Bernd Schmeck
出处
期刊:Thorax
[BMJ]
日期:2026-02-23
卷期号:: thorax-2025
被引量:1
标识
DOI:10.1136/thorax-2025-224202
摘要
Influenza A virus (IAV)-induced exacerbations are a major contributor to morbidity in chronic obstructive pulmonary disease (COPD), yet the epithelial mechanisms that govern these events remain unknown. We profiled the response to IAV infection of differentiated airway epithelial cells from healthy donors and individuals with COPD at single-cell resolution. The analysis revealed infection-driven shifts across multiple epithelial compartments and distinct alterations in cell-cell communication in COPD, associated with an increased CXCL11 expression. Functional assays demonstrated that CXCL11 augments mucus-associated gene and protein expression, particularly MUC5AC, increases mucus secretion and viscosity and is associated with reduction of virus-related immune pathways. This highlights CXCL11 as a contributor to both mucus hypersecretion and impaired antiviral epithelial responses in COPD exacerbations.
科研通智能强力驱动
Strongly Powered by AbleSci AI