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特应性皮炎中的肥胖与微生物群:过氧化物酶体增殖物激活受体γ激动剂的治疗意义

Obesity and the microbiome in atopic dermatitis: Therapeutic implications for PPAR-γ agonists.

作者信息

McAleer Jeremy P

机构信息

Department of Pharmaceutical Sciences, Marshall University School of Pharmacy, Huntington, WV, United States.

出版信息

Front Allergy. 2023 Mar 27;4:1167800. doi: 10.3389/falgy.2023.1167800. eCollection 2023.

Abstract

Atopic dermatitis (AD) is an inflammatory skin disease characterized by epidermal barrier disruption, Th2 immune responses to skin allergens and microbial dysbiosis within affected lesions. Studies within the past decade have revealed genetic and environmental factors contributing to AD in children. Obesity is a metabolic disorder that often manifests early in life and is associated with reduced bacterial diversity, leading to skin colonization with lipophilic bacteria and intestinal colonization with pro-inflammatory species. These changes impair epithelial barriers and promote Th17 responses, which may worsen the severity of AD symptoms. While few studies have examined the contribution of microbiota in obesity-induced allergies, there is emerging evidence that PPAR-γ may be an effective therapeutic target. This review discusses the microbiome in pediatric AD, treatment with probiotics, how disease is altered by obesity and potential therapeutic effects of PPAR-γ agonists. While healthy skin contains diverse species adapted for specific niches, lesional skin is highly colonized with which perpetuates the inflammatory reaction. Treatments for AD should help to restore microbial diversity in the skin and intestine, as well as epithelial barrier function. Pre-clinical models have shown that PPAR-γ agonists can suppress Th17 responses, IgE production and mast cell function, while improving the epidermal barrier and microbial homeostasis. Overall, PPAR-γ agonists may be effective in a subset of patients with AD, and future studies should distinguish their metabolic and anti-inflammatory effects in order to inform the best therapies.

摘要

特应性皮炎(AD)是一种炎症性皮肤病,其特征为表皮屏障破坏、对皮肤过敏原的Th2免疫反应以及受累皮损内的微生物生态失调。过去十年的研究揭示了导致儿童AD的遗传和环境因素。肥胖是一种代谢紊乱疾病,通常在生命早期出现,与细菌多样性降低有关,导致亲脂性细菌在皮肤定植以及促炎菌种在肠道定植。这些变化会损害上皮屏障并促进Th17反应,这可能会加重AD症状的严重程度。虽然很少有研究探讨微生物群在肥胖诱导的过敏中的作用,但越来越多的证据表明过氧化物酶体增殖物激活受体γ(PPAR-γ)可能是一个有效的治疗靶点。本综述讨论了儿童AD中的微生物组、益生菌治疗、肥胖如何改变疾病以及PPAR-γ激动剂的潜在治疗效果。健康皮肤含有适应特定微环境的多种菌种,而皮损皮肤则被大量定植,从而使炎症反应持续存在。AD的治疗应有助于恢复皮肤和肠道中的微生物多样性以及上皮屏障功能。临床前模型表明,PPAR-γ激动剂可以抑制Th17反应、IgE产生和肥大细胞功能,同时改善表皮屏障和微生物稳态。总体而言,PPAR-γ激动剂可能对一部分AD患者有效,未来的研究应区分其代谢和抗炎作用,以便为最佳治疗提供依据。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/76e8/10083318/f9cfee7ca673/falgy-04-1167800-g001.jpg

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