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趋化因子与皮肤炎症中的固有淋巴细胞

Chemokines and Innate Lymphoid Cells in Skin Inflammation.

机构信息

Center for Immunology and Inflammatory Diseases, Massachusetts General Hospital, Harvard Medical School, Boston, MA 02114, USA.

Department of Gynecological Oncology, Women's Hospital, Zhejiang University School of Medicine, Hangzhou 310006, China.

出版信息

Cells. 2021 Nov 8;10(11):3074. doi: 10.3390/cells10113074.

DOI:10.3390/cells10113074
PMID:34831296
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8621478/
Abstract

As the outermost barrier, skin plays an important role in protecting our bodies against outside invasion. Under stable conditions or during inflammation, leukocytes migration is essential for restoring homeostasis in the skin. Immune cells trafficking is orchestrated by chemokines; leukocytes express receptors that bind to chemokines and trigger migration. The homeostasis of the immune ecosystem is an extremely complicated dynamic process that requires the cooperation of innate and adaptive immune cells. Emerging studies have been shedding a light on the unique characteristics of skin-resident innate lymphoid cells (ILCs). In this review, we discuss how chemokines orchestrate skin ILCs trafficking and contribute to tissue homeostasis and how abnormal chemokine-chemokine receptor interactions contribute to and augment skin inflammation, as seen in conditions such as contact hypersensitivity, atopic dermatitis, and psoriasis.

摘要

皮肤作为人体的最外层屏障,对于抵御外界入侵起着重要作用。在稳定状态或炎症期间,白细胞的迁移对于恢复皮肤的内稳态至关重要。趋化因子协调免疫细胞的迁移;白细胞表达的受体与趋化因子结合并触发迁移。免疫生态系统的内稳态是一个极其复杂的动态过程,需要先天和适应性免疫细胞的合作。新出现的研究揭示了皮肤固有淋巴细胞(ILC)的独特特征。在这篇综述中,我们讨论了趋化因子如何协调皮肤 ILC 的迁移,以及如何促进组织内稳态,以及异常的趋化因子-趋化因子受体相互作用如何导致和加剧皮肤炎症,如接触性过敏、特应性皮炎和银屑病等疾病。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d36e/8621478/9459e15b9cce/cells-10-03074-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d36e/8621478/6cda7c967bb7/cells-10-03074-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d36e/8621478/1d9dc8b9a34d/cells-10-03074-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d36e/8621478/8412265615be/cells-10-03074-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d36e/8621478/9459e15b9cce/cells-10-03074-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d36e/8621478/6cda7c967bb7/cells-10-03074-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d36e/8621478/1d9dc8b9a34d/cells-10-03074-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d36e/8621478/8412265615be/cells-10-03074-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d36e/8621478/9459e15b9cce/cells-10-03074-g004.jpg

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J Invest Dermatol. 2021 Aug;141(8):1985-1994. doi: 10.1016/j.jid.2020.12.034. Epub 2021 Mar 2.
2
Skin-resident innate lymphoid cells converge on a pathogenic effector state.皮肤固有淋巴细胞向致病效应状态收敛。
Nature. 2021 Apr;592(7852):128-132. doi: 10.1038/s41586-021-03188-w. Epub 2021 Feb 3.
3
Skin-resident natural killer T cells participate in cutaneous allergic inflammation in atopic dermatitis.
皮肤中的自然杀伤细胞:深入了解一个被忽视的二级淋巴器官多方面特性的独特契机。
Front Immunol. 2025 Aug 12;16:1646719. doi: 10.3389/fimmu.2025.1646719. eCollection 2025.
4
Association of +67 G/A and -426 T/C Polymorphism in Eotaxin (CCL11) Gene with Psoriasis Phenotypes.嗜酸性粒细胞趋化因子(CCL11)基因 +67 G/A 和 -426 T/C 多态性与银屑病表型的关联
Genes (Basel). 2025 Feb 27;16(3):288. doi: 10.3390/genes16030288.
5
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JID Innov. 2024 Dec 17;5(2):100340. doi: 10.1016/j.xjidi.2024.100340. eCollection 2025 Mar.
6
CD4CCR5 T cells and CCL3+ mast cells are increased in the skin of patients with chronic spontaneous urticaria.慢性自发性荨麻疹患者皮肤中 CD4CCR5+T 细胞和 CCL3+肥大细胞增加。
Front Immunol. 2024 Jul 22;15:1327040. doi: 10.3389/fimmu.2024.1327040. eCollection 2024.
7
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Cells. 2024 Mar 6;13(5):462. doi: 10.3390/cells13050462.
8
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Cells. 2024 Feb 28;13(5):425. doi: 10.3390/cells13050425.
9
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Int J Mol Sci. 2023 Dec 29;25(1):478. doi: 10.3390/ijms25010478.
10
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Heliyon. 2023 Dec 10;10(1):e23542. doi: 10.1016/j.heliyon.2023.e23542. eCollection 2024 Jan 15.
皮肤固有自然杀伤 T 细胞参与特应性皮炎的皮肤过敏性炎症。
J Allergy Clin Immunol. 2021 May;147(5):1764-1777. doi: 10.1016/j.jaci.2020.11.049. Epub 2021 Jan 28.
4
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J Am Acad Dermatol. 2021 Apr;84(4):913-920. doi: 10.1016/j.jaad.2020.10.094. Epub 2020 Nov 28.
5
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J Allergy Clin Immunol. 2020 Jun;145(6):1606-1614.e4. doi: 10.1016/j.jaci.2020.02.026. Epub 2020 Mar 14.
6
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J Exp Med. 2019 Dec 2;216(12):2763-2777. doi: 10.1084/jem.20182111. Epub 2019 Sep 19.
8
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Nat Commun. 2019 Jul 29;10(1):3371. doi: 10.1038/s41467-019-11304-8.
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Nat Immunol. 2019 Aug;20(8):992-1003. doi: 10.1038/s41590-019-0423-0. Epub 2019 Jul 1.
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J Exp Med. 2019 Sep 2;216(9):1999-2009. doi: 10.1084/jem.20190689. Epub 2019 Jun 27.