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调节性T细胞对哮喘和过敏的控制

Control of Asthma and Allergy by Regulatory T Cells.

作者信息

Jheng Min-Jhen, Kita Hirohito

机构信息

Mayo Clinic Graduate School of Biomedical Sciences, Mayo Clinic Arizona, Scottsdale, Arizona, USA.

Division of Allergy, Asthma, and Clinical Immunology, Mayo Clinic Arizona, Scottsdale, Arizona, USA.

出版信息

Int Arch Allergy Immunol. 2025;186(1):87-102. doi: 10.1159/000540407. Epub 2024 Aug 16.

DOI:10.1159/000540407
PMID:39154634
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11729466/
Abstract

BACKGROUND

Epithelial barriers, such as the lungs and skin, face the challenge of providing the tissues' physiological function and maintaining tolerance to the commensal microbiome and innocuous environmental factors while defending the host against infectious microbes. Asthma and allergic diseases can result from maladaptive immune responses, resulting in exaggerated and persistent type 2 immunity and tissue inflammation.

SUMMARY

Among the diverse populations of tissue immune cells, CD4+ regulatory T cells (Treg cells) are central to controlling immune responses and inflammation and restoring tissue homeostasis. Humans and mice that are deficient in Treg cells experience extensive inflammation in their mucosal organs and skin. During past decades, major progress has been made toward understanding the immunobiology of Treg cells and the molecular and cellular mechanisms that control their differentiation and function. It is now clear that Treg cells are not a single cell type and that they demonstrate diversity and plasticity depending on their differentiation stages and tissue environment. They could also take on a proinflammatory phenotype in certain conditions.

KEY MESSAGES

Treg cells perform distinct functions, including the induction of immune tolerance, suppression of inflammation, and promotion of tissue repair. Subsets of Treg cells in mucosal tissues are regulated by their differentiation stage and tissue inflammatory milieu. Treg cell dysfunction likely plays roles in persistent immune responses and tissue inflammation in asthma and allergic diseases.

摘要

背景

上皮屏障,如肺和皮肤,面临着既要提供组织的生理功能,维持对共生微生物群和无害环境因素的耐受性,又要保护宿主抵御感染性微生物的挑战。哮喘和过敏性疾病可能源于适应性免疫反应失调,导致2型免疫反应过度且持续,以及组织炎症。

总结

在多种组织免疫细胞群体中,CD4 + 调节性T细胞(Treg细胞)对于控制免疫反应和炎症以及恢复组织稳态至关重要。缺乏Treg细胞的人类和小鼠在其黏膜器官和皮肤中会出现广泛炎症。在过去几十年中,在理解Treg细胞的免疫生物学以及控制其分化和功能的分子和细胞机制方面取得了重大进展。现在很清楚,Treg细胞不是单一的细胞类型,并且它们根据其分化阶段和组织环境表现出多样性和可塑性。在某些情况下,它们也可能呈现促炎表型。

关键信息

Treg细胞执行不同的功能,包括诱导免疫耐受、抑制炎症和促进组织修复。黏膜组织中的Treg细胞亚群受其分化阶段和组织炎症微环境的调节。Treg细胞功能障碍可能在哮喘和过敏性疾病的持续免疫反应和组织炎症中起作用。

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Immunity. 2024 Jun 11;57(6):1345-1359.e5. doi: 10.1016/j.immuni.2024.04.002. Epub 2024 Apr 30.
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Single-Cell Analysis Uncovers Striking Cellular Heterogeneity of Lung-Infiltrating Regulatory T Cells during Eosinophilic versus Neutrophilic Allergic Airway Inflammation.单细胞分析揭示了嗜酸性粒细胞与中性粒细胞性过敏性气道炎症期间肺浸润调节性 T 细胞的显著细胞异质性。
J Immunol. 2024 Jun 15;212(12):1867-1876. doi: 10.4049/jimmunol.2300646.
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Two regulatory T cell populations in the visceral adipose tissue shape systemic metabolism.
内脏脂肪组织中的两种调节性 T 细胞群塑造了全身代谢。
Nat Immunol. 2024 Mar;25(3):496-511. doi: 10.1038/s41590-024-01753-9. Epub 2024 Feb 14.
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Regulatory T cell-derived IL-1Ra suppresses the innate response to respiratory viral infection.调节性 T 细胞衍生的白细胞介素-1 受体拮抗剂抑制呼吸道病毒感染的固有免疫反应。
Nat Immunol. 2023 Dec;24(12):2091-2107. doi: 10.1038/s41590-023-01655-2. Epub 2023 Nov 9.
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Obesity-induced dysregulation of skin-resident PPARγ Treg cells promotes IL-17A-mediated psoriatic inflammation.肥胖引起的皮肤驻留 PPARγ Treg 细胞失调促进了 IL-17A 介导的银屑病炎症。
Immunity. 2023 Aug 8;56(8):1844-1861.e6. doi: 10.1016/j.immuni.2023.06.021. Epub 2023 Jul 20.
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Eosinophils from A to Z.从 A 到 Z 认识嗜酸性粒细胞。
Allergy. 2023 Jul;78(7):1810-1846. doi: 10.1111/all.15751. Epub 2023 May 7.
7
Principles of regulatory T cell function.调节性 T 细胞功能的原则。
Immunity. 2023 Feb 14;56(2):240-255. doi: 10.1016/j.immuni.2023.01.004.
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Lung-resident CD69ST2 T2 cells mediate long-term type 2 memory to inhaled antigen in mice.肺驻留 CD69ST2 T2 细胞介导小鼠吸入抗原的 2 型记忆的长期维持。
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