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肿瘤坏死因子样凋亡微弱诱导剂:重度脱发患者的一种新型血清标志物。

Tumor Necrosis Factor-like Weak Inducer of Apoptosis: A Novel Serum Marker in Patients with Severe Alopecia.

作者信息

Al Taweel Abdul-Aziz Ibrahim, Hamed Ahmed Mohamed, Abdelrahman Amira Mohamed Noureldin, Hassan Mona Nady Ibrahim

机构信息

Department of Dermatology and Andrology, Faculty of Medicine, Benha Univesity, Banha, Egypt.

Department of Clinical and Chemical Pathology, Faculty of Medicine, Benha Univesity, Banha, Egypt.

出版信息

Int J Trichology. 2019 May-Jun;11(3):113-117. doi: 10.4103/ijt.ijt_9_19.

DOI:10.4103/ijt.ijt_9_19
PMID:31360039
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6580803/
Abstract

BACKGROUND

Alopecia areata (AA) is a common form of nonscarring hair loss of scalp and/or body. Genetic predisposition, autoimmunity, and environmental factors play a major role in the etiopathogenesis of AA. Tumor necrosis factor-like weak inducer of apoptosis (TWEAK) is a multifunctional cytokine expressed on various cell types and tissues and acts through binding to its sole receptor factor-inducible 14 (Fn14). TWEAK/Fn14 activation contributes to various pathological processes, including cell proliferation and death, angiogenesis, carcinogenesis, and inflammation.

AIM

The aim of this current study was to measure serum levels of TWEAK in patients with AA and to assess the correlation between it and severity of the disease.

SUBJECTS AND METHODS

This study included 50 patients who had patchy AA, in addition to 50 apparently healthy controls. Severity of AA was assessed using Severity of Alopecia Tool Score. Serum TWEAK levels in all participants were determined using ELISA technique and were correlated with the severity of the disease.

RESULTS

Mean serum levels of TWEAK were significantly higher in AA patients, with a positive significant correlation between serum levels of TWEAK and severity of the disease.

CONCLUSION

TWEAK as a novel marker of many autoimmune inflammatory dermatological diseases, could be a promising marker in the diagnosis of AA, and also can be used as a prognostic marker for its severity.

摘要

背景

斑秃(AA)是头皮和/或身体非瘢痕性脱发的常见形式。遗传易感性、自身免疫和环境因素在斑秃的发病机制中起主要作用。肿瘤坏死因子样凋亡弱诱导剂(TWEAK)是一种在多种细胞类型和组织中表达的多功能细胞因子,通过与其唯一受体诱导因子14(Fn14)结合发挥作用。TWEAK/Fn14激活参与多种病理过程,包括细胞增殖与死亡、血管生成、致癌作用和炎症。

目的

本研究旨在测定斑秃患者血清中TWEAK水平,并评估其与疾病严重程度之间的相关性。

对象与方法

本研究纳入50例斑秃患者,另设50例健康对照。采用脱发严重程度工具评分评估斑秃严重程度。采用酶联免疫吸附测定(ELISA)技术测定所有参与者血清TWEAK水平,并将其与疾病严重程度进行相关性分析。

结果

斑秃患者血清TWEAK平均水平显著更高,血清TWEAK水平与疾病严重程度呈显著正相关。

结论

TWEAK作为许多自身免疫性炎症性皮肤病的新型标志物,可能是斑秃诊断中有前景的标志物,也可作为其严重程度的预后标志物。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b7a6/6580803/07cf4640cbe8/IJT-11-113-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b7a6/6580803/07cf4640cbe8/IJT-11-113-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b7a6/6580803/07cf4640cbe8/IJT-11-113-g001.jpg

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本文引用的文献

1
TWEAK/Fn14 Activation Contributes to the Pathogenesis of Bullous Pemphigoid.TWEAK/Fn14激活参与大疱性类天疱疮的发病机制。
J Invest Dermatol. 2017 Jul;137(7):1512-1522. doi: 10.1016/j.jid.2017.03.019. Epub 2017 Mar 27.
2
Alopecia areata.斑秃。
Nat Rev Dis Primers. 2017 Mar 16;3:17011. doi: 10.1038/nrdp.2017.11.
3
TWEAK activation of the non-canonical NF-κB signaling pathway differentially regulates melanoma and prostate cancer cell invasion.肿瘤坏死因子样弱凋亡诱导因子(TWEAK)激活非经典核因子κB(NF-κB)信号通路对黑色素瘤和前列腺癌细胞侵袭具有不同的调节作用。
Oncotarget. 2016 Dec 6;7(49):81474-81492. doi: 10.18632/oncotarget.13034.
4
Anti-TWEAK monoclonal antibodies reduce vascular damage and leucocyte infiltration in a mouse model of cutaneous reverse passive Arthus reaction.抗TWEAK单克隆抗体可减轻皮肤反向被动Arthus反应小鼠模型中的血管损伤和白细胞浸润。
Clin Exp Dermatol. 2016 Dec;41(8):871-877. doi: 10.1111/ced.12912. Epub 2016 Oct 18.
5
Soluble Fn14 Is Detected and Elevated in Mouse and Human Kidney Disease.在小鼠和人类肾脏疾病中可检测到可溶性Fn14且其水平升高。
PLoS One. 2016 May 12;11(5):e0155368. doi: 10.1371/journal.pone.0155368. eCollection 2016.
6
Role of the TWEAK/Fn14 pathway in autoimmune diseases.TWEAK/Fn14信号通路在自身免疫性疾病中的作用。
Immunol Res. 2016 Feb;64(1):44-50. doi: 10.1007/s12026-015-8761-y.
7
Serum levels of TWEAK in patients with psoriasis vulgaris.寻常型银屑病患者的血清肿瘤坏死因子样弱凋亡诱导因子水平
Cytokine. 2016 Jan;77:10-3. doi: 10.1016/j.cyto.2015.10.004. Epub 2015 Oct 22.
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TWEAK/Fn14 activation induces keratinocyte proliferation under psoriatic inflammation.TWEAK/Fn14激活在银屑病炎症状态下诱导角质形成细胞增殖。
Exp Dermatol. 2016 Jan;25(1):32-7. doi: 10.1111/exd.12820. Epub 2015 Sep 15.
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