{"title":"The lung-gut axis and airway inflammation in COPD.","authors":"Hua Huang, Shuai Huang, Xuhao He, Mingxing Wang","doi":"10.1080/08923973.2026.2746677","DOIUrl":null,"url":null,"abstract":"<p><strong>Objective: </strong>Chronic obstructive pulmonary disease (COPD) is a common lung disease characterized by multiple persistent respiratory symptoms and decreased lung function. Despite extensive research exploring the complex pathogenic mechanisms and signaling pathways underlying COPD, there are currently no effective disease-modifying drugs capable of halting or reversing progressive lung damage, standard interventions including bronchodilators, long-term oxygen therapy and pulmonary rehabilitation merely alleviate clinical symptoms while failing to arrest disease progression, accompanied by unavoidable adverse effects. Against this backdrop, microbiota-targeted interventions emerge as a promising alternative therapeutic strategy. This drives the urgent need to dissect unrecognized pathogenic pathways and develop novel prevention and treatment strategies.</p><p><strong>Methods: </strong>This narrative review summarizes recent data on gut microbiota dysregulation and gut-lung crosstalk in COPD, highlighting immune-mediated gut-lung crosstalk mechanisms, including the shared mucosal immune system and metabolite-induced modulation of pulmonary structure and function.</p><p><strong>Results: </strong>In addition to immune inflammation and hypoxia, COPD patients usually have gastrointestinal complications and gut microbiota (GM) dysregulation. Role of GM in regulating the functional development of the host immune system, and the \"gut-lung axis\" established by GM and the lung also plays a crucial role in regulating lung inflammation and airway function. This may be attributed to the shared mucosal immune system between the gut and lungs, as well as the ability of metabolites to influence lung structure and function. However, the specific pathway of this gut-lung communication in COPD is still unclear.</p><p><strong>Conclusions: </strong>This article reviews the changes of GM related to COPD, and focuses on the mechanism of GM and its metabolites in the occurrence and development of COPD from the immune pathway, so as to find new intervention targets, and highlight the emerging potential of GM interventions (diet, probiotics and prebiotics) for future clinical research and treatment of COPD.</p>","PeriodicalId":13420,"journal":{"name":"Immunopharmacology and Immunotoxicology","volume":" ","pages":"1-11"},"PeriodicalIF":3.1000,"publicationDate":"2026-10-14","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Immunopharmacology and Immunotoxicology","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1080/08923973.2026.2746677","RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"IMMUNOLOGY","Score":null,"Total":0}
引用次数: 0
Abstract
Objective: Chronic obstructive pulmonary disease (COPD) is a common lung disease characterized by multiple persistent respiratory symptoms and decreased lung function. Despite extensive research exploring the complex pathogenic mechanisms and signaling pathways underlying COPD, there are currently no effective disease-modifying drugs capable of halting or reversing progressive lung damage, standard interventions including bronchodilators, long-term oxygen therapy and pulmonary rehabilitation merely alleviate clinical symptoms while failing to arrest disease progression, accompanied by unavoidable adverse effects. Against this backdrop, microbiota-targeted interventions emerge as a promising alternative therapeutic strategy. This drives the urgent need to dissect unrecognized pathogenic pathways and develop novel prevention and treatment strategies.
Methods: This narrative review summarizes recent data on gut microbiota dysregulation and gut-lung crosstalk in COPD, highlighting immune-mediated gut-lung crosstalk mechanisms, including the shared mucosal immune system and metabolite-induced modulation of pulmonary structure and function.
Results: In addition to immune inflammation and hypoxia, COPD patients usually have gastrointestinal complications and gut microbiota (GM) dysregulation. Role of GM in regulating the functional development of the host immune system, and the "gut-lung axis" established by GM and the lung also plays a crucial role in regulating lung inflammation and airway function. This may be attributed to the shared mucosal immune system between the gut and lungs, as well as the ability of metabolites to influence lung structure and function. However, the specific pathway of this gut-lung communication in COPD is still unclear.
Conclusions: This article reviews the changes of GM related to COPD, and focuses on the mechanism of GM and its metabolites in the occurrence and development of COPD from the immune pathway, so as to find new intervention targets, and highlight the emerging potential of GM interventions (diet, probiotics and prebiotics) for future clinical research and treatment of COPD.
期刊介绍:
The journal Immunopharmacology and Immunotoxicology is devoted to pre-clinical and clinical drug discovery and development targeting the immune system. Research related to the immunoregulatory effects of various compounds, including small-molecule drugs and biologics, on immunocompetent cells and immune responses, as well as the immunotoxicity exerted by xenobiotics and drugs. Only research that describe the mechanisms of specific compounds (not extracts) is of interest to the journal.
The journal will prioritise preclinical and clinical studies on immunotherapy of disorders such as chronic inflammation, allergy, autoimmunity, cancer etc. The effects of small-drugs, vaccines and biologics against central immunological targets as well as cell-based therapy, including dendritic cell therapy, T cell adoptive transfer and stem cell therapy, are topics of particular interest. Publications pointing towards potential new drug targets within the immune system or novel technology for immunopharmacological drug development are also welcome.
With an immunoscience focus on drug development, immunotherapy and toxicology, the journal will cover areas such as infection, allergy, inflammation, tumor immunology, degenerative disorders, immunodeficiencies, neurology, atherosclerosis and more.
Immunopharmacology and Immunotoxicology will accept original manuscripts, brief communications, commentaries, mini-reviews, reviews, clinical trials and clinical cases, on the condition that the results reported are based on original, clinical, or basic research that has not been published elsewhere in any journal in any language (except in abstract form relating to paper communicated to scientific meetings and symposiums).