结核病中肺肠轴的认识进展。

IF 2.2 4区 生物学 Q3 MICROBIOLOGY
Skyler Colwell, Jorge Cervantes
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引用次数: 0

摘要

人类和动物研究支持肠-肺轴的存在,胃肠道共生体及其产物可以调节肺免疫功能。平衡健康的肠道菌群的作用及其恢复可能会影响肺部的微生物群。然而,这些证据的可靠性差异很大,许多研究都有相当大的局限性。肺结核患者肠道菌群多样性下降,以及结核分枝杆菌感染后肠道菌群的变化。感染已被报道,强调肺肠轴的双向性。这些变化可能与结核病的进展有关,影响接受抗结核治疗的患者的微生物群和免疫稳态。肠道和肺之间的相互作用越来越被认为是结核病发生、进展和治疗结果的关键调节因子。肠道微生物群通过其在巨噬细胞激活中的作用对肺部感染起保护作用,使其成为抗结核辅助治疗的一种有希望的方法。这篇小型综述综合了目前对结核病发病机制中肠-肺相互作用的理解,评估了文献的优势和局限性,澄清了共识与推测的领域,强调了研究结果仍处于初步阶段的地方,总结了抗结核治疗对微生物群落的影响,并讨论了微生物群知情干预措施改善患者预后的未来方向。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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.

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来源期刊
Fems Microbiology Letters
Fems Microbiology Letters 生物-微生物学
CiteScore
4.30
自引率
0.00%
发文量
112
审稿时长
1.9 months
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.
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