Dietary human milk oligosaccharides reduce allergic airway inflammation by modulating SCFAs level and ILC2 activity

IF 4.9 3区 医学 Q2 IMMUNOLOGY
Immunology Pub Date : 2024-08-06 DOI:10.1111/imm.13845
Xu Han, Zhongjie Wang, Hongchuan Cao, Weiwei Liu, Lijie Sun, Qiang Xiao
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Abstract

Group 2 innate lymphoid cells (ILC2s) play a crucial role in the progression of asthma, yet the regulatory mechanisms modulating ILC2 responses in asthma remain underexplored. Human milk oligosaccharides (HMOs), vital non-nutritive components of breast milk, are known to significantly shape immune system development and influence the incidence of allergic diseases. However, their impact on ILC2-driven asthma is not fully understood. Our research reveals that dietary HMOs act as potent inhibitors of ILC2 responses and allergic airway inflammation. Treatment with 2′-fucosyllactose (2'-FL) and 6′-sialyllactose (6'-SL) significantly reduced ILC2-related airway inflammation induced by papain or Alternaria alternata in mice, evidenced by decreased eosinophil (EOS) infiltration and lower IL-5 and IL-13 levels in BALF. Notably, while ILC2 expresses HMO receptors, HMO did not act directly on ILC2 but potentially modulated their activity through alterations in gut microbiota derived SCFAs. HMO treatments alleviated airway inflammation in SCFA-dependent manners, with SCFA depletion or receptor blocking reversing these beneficial effects. This study reveals the potential of dietary HMOs in managing asthma through modulation of ILC2 activity and the gut-lung axis, proposing a new therapeutic avenue that utilises the immunomodulatory capacities of nutritional components to combat respiratory diseases.

Abstract Image

膳食人乳低聚糖通过调节 SCFAs 水平和 ILC2 活性减轻过敏性气道炎症。
第 2 组先天性淋巴细胞(ILC2s)在哮喘的发展过程中起着至关重要的作用,但调节 ILC2 在哮喘中反应的调节机制仍未得到充分探索。母乳寡糖(HMOs)是母乳中重要的非营养成分,众所周知,它能显著影响免疫系统的发育,并影响过敏性疾病的发病率。然而,它们对 ILC2 驱动的哮喘的影响尚不完全清楚。我们的研究发现,膳食中的 HMOs 是 ILC2 反应和过敏性气道炎症的有效抑制剂。用 2'-fucosyllactose (2'-FL)和 6'-sialyllactose (6'-SL)治疗可显著减少木瓜蛋白酶或交替孢霉诱导的小鼠 ILC2 相关气道炎症,这体现在嗜酸性粒细胞(EOS)浸润减少以及 BALF 中 IL-5 和 IL-13 水平降低。值得注意的是,虽然 ILC2 表达 HMO 受体,但 HMO 并不直接作用于 ILC2,而是可能通过改变肠道微生物群衍生的 SCFAs 来调节其活性。HMO 治疗以 SCFA 依赖性的方式缓解了气道炎症,而 SCFA 的耗竭或受体阻断会逆转这些有益的影响。这项研究揭示了膳食 HMO 通过调节 ILC2 活性和肠道-肺轴来控制哮喘的潜力,提出了一种利用营养成分的免疫调节能力来防治呼吸系统疾病的新疗法。
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来源期刊
Immunology
Immunology 医学-免疫学
CiteScore
11.90
自引率
1.60%
发文量
175
审稿时长
4-8 weeks
期刊介绍: Immunology is one of the longest-established immunology journals and is recognised as one of the leading journals in its field. We have global representation in authors, editors and reviewers. Immunology publishes papers describing original findings in all areas of cellular and molecular immunology. High-quality original articles describing mechanistic insights into fundamental aspects of the immune system are welcome. Topics of interest to the journal include: immune cell development, cancer immunology, systems immunology/omics and informatics, inflammation, immunometabolism, immunology of infection, microbiota and immunity, mucosal immunology, and neuroimmunology. The journal also publishes commissioned review articles on subjects of topical interest to immunologists, and commissions in-depth review series: themed sets of review articles which take a 360° view of select topics at the heart of immunological research.
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