Research progress in neuroimmune disorders in atopic dermatitis

Atopic dermatitis (AD) is a chronic inflammatory skin disease with the highest incidence in the world. The main clinical manifestations are eczema-like skin lesions, pruritus and xeroderma. Recent studies have revealed that sensory neurons in the skin lesions of AD patients can interact abnormally w...

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Main Authors: XUAN Zhenquan, CHEN Xuanyi, YAO Zhirong
Format: Article
Language:zho
Published: Editorial Office of Journal of Shanghai Jiao Tong University (Medical Science) 2023-08-01
Series:Shanghai Jiaotong Daxue xuebao. Yixue ban
Subjects:
Online Access:https://xuebao.shsmu.edu.cn/article/2023/1674-8115/1674-8115-2023-43-8-1049.shtml
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author XUAN Zhenquan
CHEN Xuanyi
YAO Zhirong
author_facet XUAN Zhenquan
CHEN Xuanyi
YAO Zhirong
author_sort XUAN Zhenquan
collection DOAJ
description Atopic dermatitis (AD) is a chronic inflammatory skin disease with the highest incidence in the world. The main clinical manifestations are eczema-like skin lesions, pruritus and xeroderma. Recent studies have revealed that sensory neurons in the skin lesions of AD patients can interact abnormally with keratinocytes (KC) and immune cells, leading to neuroimmune disorders. Among them, there are two types of sensory neurons involved in neuroimmune disorders, including histaminergic and non-histaminergic sensory neurons. In neuroimmune disorders, KC and immune cells activate sensory neurons to induce pruritus by secreting proinflammatory cytokines such as interleukin-4 (IL-4), IL-13, IL-31, IL-33, and thymic stromal lymphopoietin, as well as chemokines such as C-X-C motif chemokine ligand 12 (CXCL12) and CXCL10. In addition, neuropeptides such as nerve growth factor, brain-derived neurotrophic factor and artemin secreted by KC and immune cells can induce overgrowth of sensory neurons, thereby promoting neuroimmune disorders. At the same time, the excessive release of neuropeptides such as calcitonin gene-related peptide and substance P by sensory neurons can act on KC and immune cells, thereby aggravating skin inflammation. In recent years, many drugs targeting neuroimmune disorders are in preclinical studies, clinical trials and other stages, or have been marketed for the treatment of AD. Among them, our research group has found that lidocaine, a local anesthetic, can target neuroimmune disorders and relieve pruritus and skin inflammation in AD patients. At present, the role of neuroimmune disorders in AD has not been systematically discussed. Based on this, this article reviews the types of sensory neurons involved in neuroimmune disorders, the role of KC, immune cells and sensory neurons in neuroimmune disorders, as well as the therapeutic strategies targeting neuroimmune disorders.
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spelling doaj.art-72235d74f6314c2aa90bf989ddd16c442024-02-18T02:27:25ZzhoEditorial Office of Journal of Shanghai Jiao Tong University (Medical Science)Shanghai Jiaotong Daxue xuebao. Yixue ban1674-81152023-08-014381049105510.3969/j.issn.1674-8115.2023.08.0141674-8115(2023)08-1049-07Research progress in neuroimmune disorders in atopic dermatitisXUAN ZhenquanCHEN XuanyiYAO ZhirongAtopic dermatitis (AD) is a chronic inflammatory skin disease with the highest incidence in the world. The main clinical manifestations are eczema-like skin lesions, pruritus and xeroderma. Recent studies have revealed that sensory neurons in the skin lesions of AD patients can interact abnormally with keratinocytes (KC) and immune cells, leading to neuroimmune disorders. Among them, there are two types of sensory neurons involved in neuroimmune disorders, including histaminergic and non-histaminergic sensory neurons. In neuroimmune disorders, KC and immune cells activate sensory neurons to induce pruritus by secreting proinflammatory cytokines such as interleukin-4 (IL-4), IL-13, IL-31, IL-33, and thymic stromal lymphopoietin, as well as chemokines such as C-X-C motif chemokine ligand 12 (CXCL12) and CXCL10. In addition, neuropeptides such as nerve growth factor, brain-derived neurotrophic factor and artemin secreted by KC and immune cells can induce overgrowth of sensory neurons, thereby promoting neuroimmune disorders. At the same time, the excessive release of neuropeptides such as calcitonin gene-related peptide and substance P by sensory neurons can act on KC and immune cells, thereby aggravating skin inflammation. In recent years, many drugs targeting neuroimmune disorders are in preclinical studies, clinical trials and other stages, or have been marketed for the treatment of AD. Among them, our research group has found that lidocaine, a local anesthetic, can target neuroimmune disorders and relieve pruritus and skin inflammation in AD patients. At present, the role of neuroimmune disorders in AD has not been systematically discussed. Based on this, this article reviews the types of sensory neurons involved in neuroimmune disorders, the role of KC, immune cells and sensory neurons in neuroimmune disorders, as well as the therapeutic strategies targeting neuroimmune disorders.https://xuebao.shsmu.edu.cn/article/2023/1674-8115/1674-8115-2023-43-8-1049.shtmlatopic dermatitis (ad)neuroimmunesensory neuronimmune cellkeratinocyte (kc)
spellingShingle XUAN Zhenquan
CHEN Xuanyi
YAO Zhirong
Research progress in neuroimmune disorders in atopic dermatitis
Shanghai Jiaotong Daxue xuebao. Yixue ban
atopic dermatitis (ad)
neuroimmune
sensory neuron
immune cell
keratinocyte (kc)
title Research progress in neuroimmune disorders in atopic dermatitis
title_full Research progress in neuroimmune disorders in atopic dermatitis
title_fullStr Research progress in neuroimmune disorders in atopic dermatitis
title_full_unstemmed Research progress in neuroimmune disorders in atopic dermatitis
title_short Research progress in neuroimmune disorders in atopic dermatitis
title_sort research progress in neuroimmune disorders in atopic dermatitis
topic atopic dermatitis (ad)
neuroimmune
sensory neuron
immune cell
keratinocyte (kc)
url https://xuebao.shsmu.edu.cn/article/2023/1674-8115/1674-8115-2023-43-8-1049.shtml
work_keys_str_mv AT xuanzhenquan researchprogressinneuroimmunedisordersinatopicdermatitis
AT chenxuanyi researchprogressinneuroimmunedisordersinatopicdermatitis
AT yaozhirong researchprogressinneuroimmunedisordersinatopicdermatitis