Volume 36, Issue 263 (11-2026)                   J Mazandaran Univ Med Sci 2026, 36(263): 344-356 | Back to browse issues page

XML Persian Abstract Print


Download citation:
BibTeX | RIS | EndNote | Medlars | ProCite | Reference Manager | RefWorks
Send citation to:

Asghari Ozma M, Tabibi M, Moaddab S R, Fallahi Alileh N. Postbiotics and the Gut-Lung Axis in Respiratory Infections: The Role of Microbial Metabolites and Their Regulation of Mucosal Immunity. , J Mazandaran Univ Med Sci. 2026; 36 (263) :344-356
URL: http://jmums.mazums.ac.ir/article-1-23302-en.html
Abstract:   (32 Views)
Respiratory infections, ranging from influenza and respiratory syncytial virus (RSV) infection to bacterial pneumonia, tuberculosis, and secondary infections following viral disease, are shaped by complex interactions among the gut microbiota, respiratory microbiota, and mucosal immune system. Increasing evidence suggests that the gut–lung axis is not merely an immunological communication pathway but also an active metabolic network through which microbial products regulate pulmonary epithelial and immune responses via systemic circulation, immune cell trafficking, and neural signalling. Among these products, short-chain fatty acids, particularly butyrate, acetate, and propionate, together with tryptophan-derived metabolites, secondary bile acids, and certain polyamines, modulate the functions of alveolar macrophages, dendritic cells, neutrophils, and regulatory T cells, as well as interferon production, through G protein-coupled receptor signalling, histone deacetylase inhibition, and activation of the aryl hydrocarbon receptor pathway. Infection-, antibiotic-, and diet-associated dysbiosis may reduce the production of these microbial metabolites, disrupt epithelial barrier integrity and antimicrobial peptide production, and impair pulmonary antiviral immunity, thereby increasing susceptibility to excessive inflammation and secondary bacterial infections. Against this background, postbiotics, including microbial metabolites, antimicrobial peptides, cell-wall components, polysaccharides, and extracellular vesicles derived from beneficial microorganisms, have emerged as potentially more controllable alternatives to interventions involving live microorganisms. Preclinical evidence suggests that these bioactive components may influence mucosal barrier integrity, inflammatory signalling, and host defence against respiratory pathogens. This review examines the interplay between postbiotics, microbial metabolism, and mucosal immunity. It discusses the molecular mechanisms underlying the gut–lung axis in respiratory infections and critically compares evidence from studies of influenza, RSV, SARS-CoV-2, bacterial pneumonia, and secondary infections. Particular emphasis is placed on strain- and metabolite-specific effects, the differences between live and non-living microbial interventions, translational challenges, and the need to develop targeted postbiotic strategies for precision respiratory therapeutics.

 
Full-Text [PDF 928 kb]   (16 Downloads)    
Type of Study: Review | Subject: Microbiology

Add your comments about this article : Your username or Email:
CAPTCHA

Rights and permissions
Creative Commons License This work is licensed under a Creative Commons Attribution-NonCommercial 4.0 International License.

© 2026 CC BY-NC 4.0 | Journal of Mazandaran University of Medical Sciences

Designed & Developed by : Yektaweb