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肠道通透性增加的早产儿肠道微生物组和粪便免疫表型改变。

Altered Gut Microbiome and Fecal Immune Phenotype in Early Preterm Infants With Leaky Gut.

机构信息

Department of Pediatrics, University of Maryland School of Medicine, Baltimore, MD, United States.

Center for Vaccine Development and Global Health, University of Maryland School of Medicine, Baltimore, MD, United States.

出版信息

Front Immunol. 2022 Feb 23;13:815046. doi: 10.3389/fimmu.2022.815046. eCollection 2022.

DOI:10.3389/fimmu.2022.815046
PMID:35280991
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8905226/
Abstract

Intestinal barrier immaturity, or "leaky gut", is the proximate cause of susceptibility to necrotizing enterocolitis in preterm neonates. Exacerbated intestinal immune responses, gut microbiota dysbiosis, and heightened barrier injury are considered primary triggers of aberrant intestinal maturation in early life. Inordinate host immunity contributes to this process, but the precise elements remain largely uncharacterized, leaving a significant knowledge gap in the biological underpinnings of gut maturation. In this study, we investigated the fecal cytokine profile and gut microbiota in a cohort of 40 early preterm infants <33-weeks-gestation to identify immune markers of intestinal barrier maturation. Three distinct microbiota types were demonstrated to be differentially associated with intestinal permeability (IP), maternal breast milk feeding, and immunological profiles. The and Enterobacteriaceae-predominant microbiota types were associated with an elevated IP, reduced breast milk feeding, and less defined fecal cytokine profile. On the other hand, a lower IP was associated with increased levels of fecal IL-1α/β and a microbiota type that included a wide array of anaerobes with expanded fermentative capacity. Our study demonstrated the critical role of both immunological and microbiological factors in the early development of intestinal barrier that collectively shape the intestinal microenvironment influencing gut homeostasis and postnatal intestinal maturation in early preterm newborns.

摘要

肠道屏障不成熟,又称“肠漏”,是早产儿易患坏死性小肠结肠炎的直接原因。肠道免疫反应加剧、肠道微生物失调和屏障损伤加剧被认为是早期生命中肠道成熟异常的主要触发因素。过度的宿主免疫对此过程有贡献,但确切的因素在很大程度上仍未被描述,这使得肠道成熟的生物学基础存在重大知识空白。在这项研究中,我们调查了 40 名<33 周胎龄的早期早产儿的粪便细胞因子谱和肠道微生物群,以确定肠道屏障成熟的免疫标志物。研究表明,三种不同的微生物群类型与肠道通透性(IP)、母乳喂养和免疫特征存在显著差异。和肠杆菌科为主的微生物群类型与升高的 IP、减少母乳喂养和不明确的粪便细胞因子谱相关。另一方面,较低的 IP 与粪便中 IL-1α/β 水平升高和包括具有扩展发酵能力的多种厌氧菌的微生物群类型相关。我们的研究表明,免疫和微生物因素在肠道屏障的早期发育中起着关键作用,它们共同塑造肠道微环境,影响肠道内稳态和早期早产儿的肠道成熟。

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