{"title":"Early-Life Gut Microbiota and the Pediatric Gut-Lung Axis: A Systematic Review of Clinical, Preclinical, and Mechanistic Evidence.","authors":"Salvatore Michele Carnazzo, Alessandro Vitello, Andrea Domenico Praticò, Marcello Maida, Vassilios Fanos","doi":"10.3390/nu18193260","DOIUrl":null,"url":null,"abstract":"<p><p><b>Background/Objectives:</b> The early-life gut microbiota plays a pivotal role in immune maturation and may influence respiratory health through the gut-lung axis. However, evidence linking microbial development, dysbiosis, microbial metabolites, and microbiota-targeted interventions to pediatric respiratory outcomes remains heterogeneous. This systematic review aimed to synthesize clinical and preclinical evidence on the pediatric gut-lung axis and its underlying mechanisms. <b>Methods:</b> This systematic review followed PRISMA 2020 guidelines and a prospectively registered PROSPERO protocol (CRD420251062905). PubMed, Scopus, and Web of Science were searched for studies published from January 2014 to March 2025. Eligible primary studies included randomized controlled trials, observational studies, and mechanistically relevant animal models. Risk of bias was assessed using RoB 2, the Newcastle-Ottawa Scale, and SYRCLE's tool, respectively. Reviews were examined separately to provide mechanistic and translational context without contributing to the primary evidence synthesis. <b>Results:</b> Twenty-five primary studies (11 clinical and 14 preclinical) were included in the systematic evidence synthesis, while 54 reviews provided complementary contextual evidence. Early gut and airway microbial communities showed substantial overlap after birth followed by progressive niche-specific divergence. Early-life dysbiosis, including depletion of beneficial taxa and expansion of potentially pathogenic bacteria, was associated with asthma, recurrent wheezing, respiratory infections, and neonatal lung injury. Short-chain fatty acids emerged as key mediators of gut-lung immune signaling. Clinical trials suggested potential respiratory and immunological benefits of probiotic and synbiotic interventions, while preclinical models supported mechanistic links involving intestinal barrier dysfunction, microbial metabolites, and inflammatory pathways. <b>Conclusions:</b> Current evidence supports a biologically plausible and clinically relevant pediatric gut-lung axis. However, methodological heterogeneity and the limited availability of longitudinal clinical studies warrant cautious interpretation and further well-designed research before microbiota-targeted strategies can be routinely translated into pediatric respiratory care.</p>","PeriodicalId":19486,"journal":{"name":"Nutrients","volume":"18 19","pages":""},"PeriodicalIF":5.8000,"publicationDate":"2026-10-02","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC13666610/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Nutrients","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.3390/nu18193260","RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"NUTRITION & DIETETICS","Score":null,"Total":0}
引用次数: 0
Abstract
Background/Objectives: The early-life gut microbiota plays a pivotal role in immune maturation and may influence respiratory health through the gut-lung axis. However, evidence linking microbial development, dysbiosis, microbial metabolites, and microbiota-targeted interventions to pediatric respiratory outcomes remains heterogeneous. This systematic review aimed to synthesize clinical and preclinical evidence on the pediatric gut-lung axis and its underlying mechanisms. Methods: This systematic review followed PRISMA 2020 guidelines and a prospectively registered PROSPERO protocol (CRD420251062905). PubMed, Scopus, and Web of Science were searched for studies published from January 2014 to March 2025. Eligible primary studies included randomized controlled trials, observational studies, and mechanistically relevant animal models. Risk of bias was assessed using RoB 2, the Newcastle-Ottawa Scale, and SYRCLE's tool, respectively. Reviews were examined separately to provide mechanistic and translational context without contributing to the primary evidence synthesis. Results: Twenty-five primary studies (11 clinical and 14 preclinical) were included in the systematic evidence synthesis, while 54 reviews provided complementary contextual evidence. Early gut and airway microbial communities showed substantial overlap after birth followed by progressive niche-specific divergence. Early-life dysbiosis, including depletion of beneficial taxa and expansion of potentially pathogenic bacteria, was associated with asthma, recurrent wheezing, respiratory infections, and neonatal lung injury. Short-chain fatty acids emerged as key mediators of gut-lung immune signaling. Clinical trials suggested potential respiratory and immunological benefits of probiotic and synbiotic interventions, while preclinical models supported mechanistic links involving intestinal barrier dysfunction, microbial metabolites, and inflammatory pathways. Conclusions: Current evidence supports a biologically plausible and clinically relevant pediatric gut-lung axis. However, methodological heterogeneity and the limited availability of longitudinal clinical studies warrant cautious interpretation and further well-designed research before microbiota-targeted strategies can be routinely translated into pediatric respiratory care.
背景/目的:生命早期肠道微生物群在免疫成熟中起关键作用,并可能通过肠-肺轴影响呼吸系统健康。然而,将微生物发育、生态失调、微生物代谢物和微生物群靶向干预与儿科呼吸结果联系起来的证据仍然不一致。本系统综述旨在综合小儿肠-肺轴及其潜在机制的临床和临床前证据。方法:本系统评价遵循PRISMA 2020指南和前瞻性注册的PROSPERO协议(CRD420251062905)。PubMed、Scopus和Web of Science检索了2014年1月至2025年3月发表的研究。符合条件的初步研究包括随机对照试验、观察性研究和与机械相关的动物模型。分别使用RoB 2、Newcastle-Ottawa量表和sycle工具评估偏倚风险。综述分别进行审查,以提供机制和翻译背景,而不促进主要证据的综合。结果:25项初步研究(11项临床研究和14项临床前研究)被纳入系统证据合成,54篇综述提供了补充的背景证据。出生后,早期肠道和气道微生物群落显示出大量重叠,随后出现了逐渐的生态位特异性分化。生命早期生态失调,包括有益类群的消耗和潜在致病菌的扩增,与哮喘、复发性喘息、呼吸道感染和新生儿肺损伤有关。短链脂肪酸成为肠-肺免疫信号传导的关键介质。临床试验表明,益生菌和合成菌干预可能对呼吸和免疫系统有益,而临床前模型支持涉及肠道屏障功能障碍、微生物代谢物和炎症途径的机制联系。结论:目前的证据支持生物学上合理和临床相关的儿科肠-肺轴。然而,方法学的异质性和纵向临床研究的有限可用性需要谨慎的解释和进一步精心设计的研究,然后才能将针对微生物群的策略常规地转化为儿科呼吸护理。
期刊介绍:
Nutrients (ISSN 2072-6643) is an international, peer-reviewed open access advanced forum for studies related to Human Nutrition. It publishes reviews, regular research papers and short communications. Our aim is to encourage scientists to publish their experimental and theoretical results in as much detail as possible. There is no restriction on the length of the papers. The full experimental details must be provided so that the results can be reproduced.