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寻常型银屑病患者外周血单个核细胞死亡受体 3 的表达。

Expression of death receptor 3 (DR3) on peripheral blood mononuclear cells of patients with psoriasis vulgaris.

机构信息

Department of Dermatology, Chengdu Second People's Hospital, Chengdu, China.

Department of Dermatology, Chengdu Second People's Hospital, Chengdu, China

出版信息

Postgrad Med J. 2018 Oct;94(1116):551-555. doi: 10.1136/postgradmedj-2018-136040. Epub 2018 Oct 19.

Abstract

BACKGROUND

A series of previous reports indicated that tumour necrosis factor-like ligand 1A (TL1A) and its receptor death receptor 3 (DR3) are involved in the pathogenesis of psoriasis vulgaris (PV), which is a common chronic skin disease accompanied by a number of comorbidities, although their exact roles remain unclear. Our previous studies demonstrated that serum TL1A levels were substantially elevated in patients with PV, but the detection of DR3 expression in peripheral blood mononuclear cells (PBMCs) of patients with PV had not been reported. Therefore, we detected DR3 expression on CD4+, CD8+, CD14+ and CD19+ PBMCs of patients with PV, atopic dermatitis (AD) and healthy volunteers.

METHODS

Blood samples were collected from participants with PV before and after treatment. Then, PBMCs from patients with PV were isolated. The Psoriasis Area Severity Index (PASI) was used to assess severity in patients with PV. The DR3 on CD4+, CD8+, CD14+ and CD19+ PBMCs were detected by flow cytometry analysis. Pearson's correlation analysis was then used to investigate the relationship between DR3 expression and PASI scores in patients with PV.

RESULTS

Comparing with the healthy volunteers and patients with AD, the percentage of DR3-expressing on CD8+ and CD14+ PBMCs in patients with PV was elevated, but the percentage of DR3-expressing on CD8+ and CD14+ cells decreased after anti-inflammatory treatment, which was correlated with PASI scores.

CONCLUSIONS

Taken together, these findings suggest that DR3 may play a key role in the pathogenesis of PV.

摘要

背景

一系列先前的报告表明,肿瘤坏死因子样配体 1A(TL1A)及其受体死亡受体 3(DR3)参与了寻常型银屑病(PV)的发病机制,PV 是一种常见的慢性皮肤病,伴有多种合并症,尽管其确切作用尚不清楚。我们之前的研究表明,PV 患者的血清 TL1A 水平显著升高,但尚未报道 PV 患者外周血单个核细胞(PBMC)中 DR3 的表达情况。因此,我们检测了 PV、特应性皮炎(AD)患者和健康志愿者的 CD4+、CD8+、CD14+和 CD19+PBMC 上的 DR3 表达。

方法

采集 PV 患者治疗前后的血样。然后,从 PV 患者中分离 PBMC。使用银屑病面积严重程度指数(PASI)评估 PV 患者的严重程度。通过流式细胞术分析检测 CD4+、CD8+、CD14+和 CD19+PBMC 上的 DR3。然后,采用 Pearson 相关分析来研究 DR3 表达与 PV 患者 PASI 评分之间的关系。

结果

与健康志愿者和 AD 患者相比,PV 患者 CD8+和 CD14+PBMC 上表达 DR3 的比例升高,但抗炎治疗后 CD8+和 CD14+细胞上表达 DR3 的比例降低,且与 PASI 评分相关。

结论

综上所述,这些发现表明 DR3 可能在 PV 的发病机制中发挥关键作用。

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