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评价甲氨蝶呤治疗后银屑病患者基质细胞衍生因子-1 ɑ(CXCL12)的表达。

Evaluation of the expression of the stromal cell-derived factor-1 alpha (CXCL 12) in psoriatic patients after treatment with Methotrexate.

机构信息

Department of Dermatology, Faculty of Medicine for Girls, Al Azhar University, Cairo, Egypt.

Department of Pathology, Faculty of Medicine, Ain Shams University, Cairo, Egypt.

出版信息

J Cosmet Dermatol. 2020 Jan;19(1):253-258. doi: 10.1111/jocd.12994. Epub 2019 May 22.

Abstract

BACKGROUND

CXCL12 has an important role in skin homeostasis and inflammation.

OBJECTIVE

In this work, the expression of CXCL12 was evaluated in psoriasis vulgaris, psoriatic arthritis (PsA) patients in relation to disease activity and methotrexate (MTX) therapy.

METHODS

Skin biopsies were obtained from 10 psoriasis vulgaris patients, 10 PsA patients, and 20 controls. The biopsies were repeated 6 weeks after MTX therapy. The biopsies were stained immunohistochemically by stromal dermal factor 1 alpha (CXCL 12) antibody.

RESULTS

Psoriatic arthritis showed significantly more expression of CXCL 12 than psoriasis vulgaris patients before treatment but not after treatment. There was significant decrease in CXCL 12 expression in the keratinocytes of psoriasis vulgaris patients after MTX therapy than before treatment, P-value was 0.009. There was no significant difference between pre- and post-treatment in the CXCL 12 expression of keratinocytes of PsA patients, P-value was 0.093. The percentage decrease of PASI score after treatment showed a moderate correlation with the percentage decrease of CXCL12 expression of the keratinocytes of the total psoriasis patients, r = 0.484, P-value was 0.015.

CONCLUSION

CXCL12 might be involved in the progression of psoriasis vulgaris to PsA. MTX therapy downregulated the expression of CXCL12 of the keratinocytes of psoriasis patients. This downregulation was paralleled by decrease in the PASI score. CXCL12 can be used as a biological marker of disease severity of psoriasis patients.

摘要

背景

趋化因子 CXCL12 在皮肤稳态和炎症中具有重要作用。

目的

本研究评估了寻常型银屑病、银屑病关节炎(PsA)患者中 CXCL12 的表达与疾病活动和甲氨蝶呤(MTX)治疗的关系。

方法

从 10 例寻常型银屑病患者、10 例 PsA 患者和 20 例对照者中获取皮肤活检组织。在 MTX 治疗 6 周后对活检组织进行重复评估。通过基质细胞衍生因子 1 阿尔法(CXCL12)抗体对活检组织进行免疫组织化学染色。

结果

在治疗前,PsA 患者的 CXCL12 表达显著高于寻常型银屑病患者,但治疗后无差异。与治疗前相比,MTX 治疗后寻常型银屑病患者的角质形成细胞中 CXCL12 的表达显著下降,P 值为 0.009。治疗前后,PsA 患者角质形成细胞中 CXCL12 的表达无显著差异,P 值为 0.093。治疗后 PASI 评分下降百分比与寻常型银屑病患者角质形成细胞中 CXCL12 表达下降百分比呈中度相关,r=0.484,P 值为 0.015。

结论

CXCL12 可能参与了寻常型银屑病向 PsA 的进展。MTX 治疗下调了寻常型银屑病患者角质形成细胞中 CXCL12 的表达。这种下调与 PASI 评分的下降平行。CXCL12 可作为评估银屑病患者疾病严重程度的生物学标志物。

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