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Increased serum levels of CCL3, CXCL8, CXCL9, and CXCL10 in rosacea patients and their correlation with disease severity

CXCL9型 酒渣鼻 趋化因子 CXCL11型 CXCL10型 红斑 白细胞介素8 免疫学 趋化因子受体 医学 CXCR3型 疾病 相关性 疾病严重程度 趋化因子受体 银屑病 内科学 正相关 胃肠病学 病例对照研究 皮肤病科
作者
Tangxiele Liu,Ji Li,Zhili Deng,Mengting Chen,Ke Sha,Wenqin Xiao,Hongfu Xie,Zhixiang Zhao
出处
期刊:Journal of Dermatology [Wiley]
卷期号:49 (5): 525-533 被引量:13
标识
DOI:10.1111/1346-8138.16329
摘要

Abstract Rosacea is a common chronic inflammatory skin disease involving millions of patients worldwide. Previous studies have highlighted the upregulation of a variety of chemokines in the skin lesions of both rosacea patient and rosacea‐like mouse model. However, the serum levels of these chemokines and their clinical significance have not been explored before. In this study, we aimed at examining the serum levels of a series of chemokines (including CCL2, CCL3, CCL20, CXCL1, CXCL8, CXCL9, CXCL10, and CXCL12) implicated in rosacea and their correlation with disease severity. Bio‐Plex Pro Human Chemokine Assays were used to measure the serum levels of these chemokines. Investigator’s Global Assessment (IGA) was applied for assessing the papules/pustules of rosacea patients, while persistent erythema was evaluated by the Clinician’s Erythema Assessment (CEA). Our results revealed that the serum concentration of CCL3, CXCL8, CXCL9, and CXCL10 were markedly elevated in rosacea patients compared to healthy controls. Among them, the levels of CCL3, CXCL8, and CXCL9 were positively correlated with the IGA score, while serum CXCL9 and CXCL10 were positively related with the CEA score of rosacea patients. What’s more, the expression of the corresponding receptors of CCL3 (Ccr1), CXCL8 (Cxcr1 and Cxcr2), CXCL9, and CXCL10 (Cxcr3) were all significantly increased in the skin lesions of rosacea‐like mouse model with CXCR2 and CXCR3 highly expressed in rosacea patient skins. Our results indicated that CCL3, CXCL8, CXCL9, and CXCL10 might potentially serve as serum indicators for rosacea and could assist the severity evaluation of disease. Findings in this study would also potentially help to develop new targeted therapies for rosacea in future. © 2022 Japanese Dermatological Association
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