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特应性皮炎中的中性粒细胞

Neutrophils in Atopic Dermatitis.

作者信息

Chiang Chih-Chao, Cheng Wei-Jen, Dela Cruz Joseph Renz Marion Santiago, Raviraj Thiyagarajan, Wu Nan-Lin, Korinek Michal, Hwang Tsong-Long

机构信息

Department of Nutrition and Health Sciences, College of Human Ecology, Chang Gung University of Science and Technology, Taoyuan, Taiwan.

Puxin Fengze Chinese Medicine Clinic, Taoyuan, Taiwan.

出版信息

Clin Rev Allergy Immunol. 2024 Dec;67(1-3):21-39. doi: 10.1007/s12016-024-09004-3. Epub 2024 Sep 18.

DOI:10.1007/s12016-024-09004-3
PMID:39294505
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11638293/
Abstract

Neutrophils have a critical role in inflammation. Recent studies have identified their distinctive presence in certain types of atopic dermatitis (AD), yet their exact function remains unclear. This review aims to compile studies elucidating the role of neutrophils in AD pathophysiology. Proteins released by neutrophils, including myeloperoxidase, elastase, and lipocalin, contribute to pruritus progression in AD. Neutrophilic oxidative stress and the formation of neutrophil extracellular traps may further worsen AD. Elevated neutrophil elastase and high-mobility group box 1 protein expression in AD patients' skin exacerbates epidermal barrier defects. Neutrophil-mast cell interactions in allergic inflammation steer the immunological response toward Th2 imbalance and activate the Th17 pathway, particularly in response to allergens or infections linked to AD. Notably, drugs alleviating pruritic symptoms in AD inhibit neutrophilic inflammation. In conclusion, these findings underscore that neutrophils may be therapeutic targets for AD symptoms, emphasizing their inclusion in AD treatment strategies.

摘要

中性粒细胞在炎症中起关键作用。最近的研究已确定它们在某些类型的特应性皮炎(AD)中独特存在,但其确切功能仍不清楚。本综述旨在汇总阐明中性粒细胞在AD病理生理学中作用的研究。中性粒细胞释放的蛋白质,包括髓过氧化物酶、弹性蛋白酶和脂质运载蛋白,会促进AD中的瘙痒进展。中性粒细胞氧化应激和中性粒细胞胞外陷阱的形成可能会使AD进一步恶化。AD患者皮肤中中性粒细胞弹性蛋白酶和高迁移率族蛋白B1表达升高会加剧表皮屏障缺陷。过敏炎症中的中性粒细胞 - 肥大细胞相互作用会使免疫反应趋向于Th2失衡并激活Th17途径,特别是在对与AD相关的过敏原或感染作出反应时。值得注意的是,减轻AD瘙痒症状的药物可抑制中性粒细胞炎症。总之,这些发现强调中性粒细胞可能是AD症状的治疗靶点,突出了将它们纳入AD治疗策略的重要性。

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本文引用的文献

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Advancements in the Study of the Immune Molecule NKp46 in Immune System-related Diseases.免疫系统相关疾病中免疫分子NKp46的研究进展
Clin Rev Allergy Immunol. 2024 Dec;67(1-3):96-110. doi: 10.1007/s12016-024-09010-5. Epub 2024 Nov 29.
2
Atopic Dermatitis and Psoriasis: Similarities and Differences in Metabolism and Microbiome.特应性皮炎和银屑病:代谢和微生物组的异同。
Clin Rev Allergy Immunol. 2024 Jun;66(3):294-315. doi: 10.1007/s12016-024-08995-3. Epub 2024 Jul 2.
3
Staphylococcus aureus Serine protease-like protein A (SplA) induces IL-8 by keratinocytes and synergizes with IL-17A.
金黄色葡萄球菌丝氨酸蛋白酶样蛋白 A(SplA)可诱导角质形成细胞产生白细胞介素-8(IL-8),并与白细胞介素-17A 协同作用。
Cytokine. 2024 Aug;180:156634. doi: 10.1016/j.cyto.2024.156634. Epub 2024 May 28.
4
SIRT1-Mediated HMGB1 Deacetylation Suppresses Neutrophil Extracellular Traps Related to Blood-Brain Barrier Impairment After Cerebral Venous Thrombosis.SIRT1 介导的 HMGB1 去乙酰化抑制了脑静脉血栓形成后与血脑屏障损伤相关的中性粒细胞胞外诱捕。
Mol Neurobiol. 2024 Aug;61(8):6060-6076. doi: 10.1007/s12035-024-03959-2. Epub 2024 Jan 25.
5
Treatment of atopic dermatitis: Recently approved drugs and advanced clinical development programs.特应性皮炎的治疗:近期获批药物和先进的临床开发项目。
Allergy. 2024 Jun;79(6):1501-1515. doi: 10.1111/all.16009. Epub 2024 Jan 8.
6
A study about how many people around the world have atopic dermatitis.一项关于全球有多少人患有特应性皮炎的研究。
Br J Dermatol. 2023 Dec 20;190(1):e6. doi: 10.1093/bjd/ljad462.
7
Neutrophil recruitment by CD4 tissue-resident memory T cells induces chronic recurrent inflammation in atopic dermatitis.CD4 组织驻留记忆 T 细胞募集中性粒细胞导致特应性皮炎的慢性复发性炎症。
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8
Neutrophil extracellular traps enhance S. aureus skin colonization by oxidative stress induction and downregulation of epidermal barrier genes.中性粒细胞胞外诱捕网通过氧化应激诱导和表皮屏障基因下调增强金黄色葡萄球菌皮肤定植。
Cell Rep. 2023 Oct 31;42(10):113148. doi: 10.1016/j.celrep.2023.113148. Epub 2023 Sep 19.
9
Global epidemiology of atopic dermatitis: a comprehensive systematic analysis and modelling study.特应性皮炎的全球流行病学:一项综合系统分析和建模研究。
Br J Dermatol. 2023 Dec 20;190(1):55-61. doi: 10.1093/bjd/ljad339.
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