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Cytokines and Epidermal Lipid Abnormalities in Atopic Dermatitis: A Systematic Review
被引:15
|作者:
Upadhyay, Parth R.
[1
]
Seminario-Vidal, Lucia
[1
]
Abe, Brian
[1
]
Ghobadi, Cyrus
[1
]
Sims, Jonathan T.
[1
]
Bunnell, Bruce A.
Panaro, Maria Antonietta
机构:
[1] Eli Lilly & Co, Lilly Corp Ctr, Indianapolis, IN 46285 USA
来源:
关键词:
cytokines;
atopic dermatitis;
lipids;
skin barrier;
barrier dysfunction;
ceramides;
fatty acid;
cholesterol;
STRATUM-CORNEUM LIPIDS;
DOWN-REGULATES FILAGGRIN;
BARRIER FUNCTION;
TH2;
CYTOKINES;
TOPICAL APPLICATION;
ACID-SPHINGOMYELINASE;
SIGNAL TRANSDUCER;
SKIN BARRIER;
CERAMIDE;
EXPRESSION;
D O I:
10.3390/cells12242793
中图分类号:
Q2 [细胞生物学];
学科分类号:
071009 ;
090102 ;
摘要:
Atopic dermatitis (AD) is the most common chronic inflammatory skin disease and presents a major public health problem worldwide. It is characterized by a recurrent and/or chronic course of inflammatory skin lesions with intense pruritus. Its pathophysiologic features include barrier dysfunction, aberrant immune cell infiltration, and alterations in the microbiome that are associated with genetic and environmental factors. There is a complex crosstalk between these components, which is primarily mediated by cytokines. Epidermal barrier dysfunction is the hallmark of AD and is caused by the disruption of proteins and lipids responsible for establishing the skin barrier. To better define the role of cytokines in stratum corneum lipid abnormalities related to AD, we conducted a systematic review of biomedical literature in PubMed from its inception to 5 September 2023. Consistent with the dominant TH2 skewness seen in AD, type 2 cytokines were featured prominently as possessing a central role in epidermal lipid alterations in AD skin. The cytokines associated with TH1 and TH17 were also identified to affect barrier lipids. Considering the broad cytokine dysregulation observed in AD pathophysiology, understanding the role of each of these in lipid abnormalities and barrier dysfunction will help in developing therapeutics to best achieve barrier homeostasis in AD patients.
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页数:16
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