{"title":"结核病中肺肠轴的认识进展。","authors":"Skyler Colwell, Jorge Cervantes","doi":"10.1093/femsle/fnaf106","DOIUrl":null,"url":null,"abstract":"<p><p>Human and animal studies have supported the existence of the gut-lung axis, where gastrointestinal commensals and their products can modulate lung immune function. The role of a balanced healthy gut microbiota, and its restoration may impact the microbiota in the lung. Yet the robustness of this evidence varies considerably, with many studies having considerable limitations. Intestinal microbiota diversity is decreased in pulmonary TB patients, and changes in the intestinal microbiota after M. tuberculosis. infection have been reported, underscoring the bidirectionality of the lung-gut axis. These changes may be associated with the progression of TB, influencing the microbiota and immunity homeostasis in those receiving anti-TB treatment. The crosstalk between the gut and the lung is increasingly recognized as a key modulator in the development, progression, and treatment outcomes of tuberculosis (TB). A protective role of the intestinal microbiota against lung infections through its role in macrophage activation, makes it a promising approach as anti-TB adjunct therapy. This mini review synthesizes current understanding of gut-lung interactions in TB pathogenesis, appraising strengths and limitations of the literature, clarifying areas of consensus versus speculation, highlighting where findings remain preliminary, summarizing the impact of anti-TB treatment on microbial communities, and discussing future directions for microbiota-informed interventions to improve patient outcomes.</p>","PeriodicalId":12214,"journal":{"name":"Fems Microbiology Letters","volume":" ","pages":""},"PeriodicalIF":2.2000,"publicationDate":"2025-10-03","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Advances in our understanding of the lung-gut axis in tuberculosis.\",\"authors\":\"Skyler Colwell, Jorge Cervantes\",\"doi\":\"10.1093/femsle/fnaf106\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>Human and animal studies have supported the existence of the gut-lung axis, where gastrointestinal commensals and their products can modulate lung immune function. The role of a balanced healthy gut microbiota, and its restoration may impact the microbiota in the lung. Yet the robustness of this evidence varies considerably, with many studies having considerable limitations. Intestinal microbiota diversity is decreased in pulmonary TB patients, and changes in the intestinal microbiota after M. tuberculosis. infection have been reported, underscoring the bidirectionality of the lung-gut axis. These changes may be associated with the progression of TB, influencing the microbiota and immunity homeostasis in those receiving anti-TB treatment. The crosstalk between the gut and the lung is increasingly recognized as a key modulator in the development, progression, and treatment outcomes of tuberculosis (TB). A protective role of the intestinal microbiota against lung infections through its role in macrophage activation, makes it a promising approach as anti-TB adjunct therapy. This mini review synthesizes current understanding of gut-lung interactions in TB pathogenesis, appraising strengths and limitations of the literature, clarifying areas of consensus versus speculation, highlighting where findings remain preliminary, summarizing the impact of anti-TB treatment on microbial communities, and discussing future directions for microbiota-informed interventions to improve patient outcomes.</p>\",\"PeriodicalId\":12214,\"journal\":{\"name\":\"Fems Microbiology Letters\",\"volume\":\" \",\"pages\":\"\"},\"PeriodicalIF\":2.2000,\"publicationDate\":\"2025-10-03\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Fems Microbiology Letters\",\"FirstCategoryId\":\"99\",\"ListUrlMain\":\"https://doi.org/10.1093/femsle/fnaf106\",\"RegionNum\":4,\"RegionCategory\":\"生物学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q3\",\"JCRName\":\"MICROBIOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Fems Microbiology Letters","FirstCategoryId":"99","ListUrlMain":"https://doi.org/10.1093/femsle/fnaf106","RegionNum":4,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"MICROBIOLOGY","Score":null,"Total":0}
Advances in our understanding of the lung-gut axis in tuberculosis.
Human and animal studies have supported the existence of the gut-lung axis, where gastrointestinal commensals and their products can modulate lung immune function. The role of a balanced healthy gut microbiota, and its restoration may impact the microbiota in the lung. Yet the robustness of this evidence varies considerably, with many studies having considerable limitations. Intestinal microbiota diversity is decreased in pulmonary TB patients, and changes in the intestinal microbiota after M. tuberculosis. infection have been reported, underscoring the bidirectionality of the lung-gut axis. These changes may be associated with the progression of TB, influencing the microbiota and immunity homeostasis in those receiving anti-TB treatment. The crosstalk between the gut and the lung is increasingly recognized as a key modulator in the development, progression, and treatment outcomes of tuberculosis (TB). A protective role of the intestinal microbiota against lung infections through its role in macrophage activation, makes it a promising approach as anti-TB adjunct therapy. This mini review synthesizes current understanding of gut-lung interactions in TB pathogenesis, appraising strengths and limitations of the literature, clarifying areas of consensus versus speculation, highlighting where findings remain preliminary, summarizing the impact of anti-TB treatment on microbial communities, and discussing future directions for microbiota-informed interventions to improve patient outcomes.
期刊介绍:
FEMS Microbiology Letters gives priority to concise papers that merit rapid publication by virtue of their originality, general interest and contribution to new developments in microbiology. All aspects of microbiology, including virology, are covered.
2019 Impact Factor: 1.987, Journal Citation Reports (Source Clarivate, 2020)
Ranking: 98/135 (Microbiology)
The journal is divided into eight Sections:
Physiology and Biochemistry (including genetics, molecular biology and ‘omic’ studies)
Food Microbiology (from food production and biotechnology to spoilage and food borne pathogens)
Biotechnology and Synthetic Biology
Pathogens and Pathogenicity (including medical, veterinary, plant and insect pathogens – particularly those relating to food security – with the exception of viruses)
Environmental Microbiology (including ecophysiology, ecogenomics and meta-omic studies)
Virology (viruses infecting any organism, including Bacteria and Archaea)
Taxonomy and Systematics (for publication of novel taxa, taxonomic reclassifications and reviews of a taxonomic nature)
Professional Development (including education, training, CPD, research assessment frameworks, research and publication metrics, best-practice, careers and history of microbiology)
If you are unsure which Section is most appropriate for your manuscript, for example in the case of transdisciplinary studies, we recommend that you contact the Editor-In-Chief by email prior to submission. Our scope includes any type of microorganism - all members of the Bacteria and the Archaea and microbial members of the Eukarya (yeasts, filamentous fungi, microbial algae, protozoa, oomycetes, myxomycetes, etc.) as well as all viruses.