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本文引用的文献

1
Current knowledge on biomarkers for contact sensitization and allergic contact dermatitis.接触致敏和过敏性接触性皮炎的生物标志物的现有知识。
Contact Dermatitis. 2017 Jul;77(1):1-16. doi: 10.1111/cod.12789. Epub 2017 May 12.
2
Proteomics analysis of dendritic cell activation by contact allergens reveals possible biomarkers regulated by Nrf2.接触性变应原激活树突状细胞的蛋白质组学分析揭示了受Nrf2调控的潜在生物标志物。
Toxicol Appl Pharmacol. 2016 Dec 15;313:170-179. doi: 10.1016/j.taap.2016.11.001. Epub 2016 Nov 3.
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A proteomic approach for the identification of immunotoxic properties of Tulipalin A.一种用于鉴定郁金香素A免疫毒性特性的蛋白质组学方法。
Proteomics. 2016 Dec;16(23):2997-3008. doi: 10.1002/pmic.201600130. Epub 2016 Nov 15.
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Can currently available non-animal methods detect pre and pro-haptens relevant for skin sensitization?目前可用的非动物方法能否检测出与皮肤致敏相关的前体半抗原和原半抗原?
Regul Toxicol Pharmacol. 2016 Dec;82:147-155. doi: 10.1016/j.yrtph.2016.08.007. Epub 2016 Aug 26.
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Contact dermatitis: in pursuit of sensitizer's molecular targets through proteomics.接触性皮炎:通过蛋白质组学寻找敏化剂的分子靶标。
Arch Toxicol. 2017 Feb;91(2):811-825. doi: 10.1007/s00204-016-1714-y. Epub 2016 Apr 29.
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Assessment of Pre- and Pro-haptens Using Nonanimal Test Methods for Skin Sensitization.使用非动物皮肤致敏试验方法评估前体半抗原和半抗原原
Chem Res Toxicol. 2016 May 16;29(5):901-13. doi: 10.1021/acs.chemrestox.6b00055. Epub 2016 Apr 29.
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Phospholipidomic Profile Variation on THP-1 Cells Exposed to Skin or Respiratory Sensitizers and Respiratory Irritant.暴露于皮肤或呼吸道致敏剂及呼吸道刺激物的THP-1细胞的磷脂组学特征变化
J Cell Physiol. 2016 Dec;231(12):2639-51. doi: 10.1002/jcp.25365. Epub 2016 Apr 4.
8
Discrimination of skin sensitizers from non-sensitizers by interleukin-1α and interleukin-6 production on cultured human keratinocytes.通过培养的人角质形成细胞产生的白细胞介素-1α和白细胞介素-6来区分皮肤致敏剂和非致敏剂。
J Appl Toxicol. 2016 Sep;36(9):1129-36. doi: 10.1002/jat.3274. Epub 2015 Dec 22.
9
IL-31 and IL-33 circulating levels in allergic contact dermatitis.过敏性接触性皮炎中白细胞介素-31和白细胞介素-33的循环水平
Eur Ann Allergy Clin Immunol. 2015 Sep;47(5):156-8.
10
In Vitro Priming of Naı̈ve T-cells with p-Phenylenediamine and Bandrowski's Base.用对苯二胺和班德罗夫斯基碱对初始T细胞进行体外致敏
Chem Res Toxicol. 2015 Oct 19;28(10):2069-77. doi: 10.1021/acs.chemrestox.5b00294. Epub 2015 Sep 21.

蛋白质组学在阐明化学介导的过敏性接触性皮炎中的应用。

Application of proteomics in the elucidation of chemical-mediated allergic contact dermatitis.

作者信息

Höper Tessa, Mussotter Franz, Haase Andrea, Luch Andreas, Tralau Tewes

机构信息

German Federal Institute for Risk Assessment , Department of Chemical and Product Safety , Max-Dohrn-Strasse 8-10 , 10589 Berlin , Germany . Email:

出版信息

Toxicol Res (Camb). 2017 Jun 13;6(5):595-610. doi: 10.1039/c7tx00058h. eCollection 2017 Sep 1.

DOI:10.1039/c7tx00058h
PMID:30090528
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6062186/
Abstract

Allergic contact dermatitis (ACD) is a widespread hypersensitivity reaction of the skin. The cellular mechanisms underlying its development are complex and involve close interaction of different cell types of the immune system. It is this very complexity which has long prevented straightforward replacement of the corresponding regulatory tests. Recent efforts have already resulted in the development of several testing alternatives that address key steps of ACD. Yet identification of suitable biomarkers is still a subject of intense research. Search strategies for the latter encompass transcriptomics, proteomics as well as metabolomics approaches. The scope of this review shall be the application and use of proteomics in the context of ACD. This includes highlighting relevant aspects of the molecular and cellular mechanisms underlying ACD, the exploitation of these mechanisms for testing and biomarkers (, in the context of the OECD's adverse outcome pathway initiative) as well as an outlook on emerging proteome targets, for example during the allergen-induced activation of dendritic cells (DCs).

摘要

过敏性接触性皮炎(ACD)是一种广泛存在的皮肤超敏反应。其发生的细胞机制复杂,涉及免疫系统不同细胞类型之间的密切相互作用。正是这种复杂性长期以来阻碍了相应常规检测方法的直接替代。最近的努力已经促成了几种针对ACD关键步骤的检测替代方法的开发。然而,合适生物标志物的鉴定仍然是深入研究的课题。寻找生物标志物的策略包括转录组学、蛋白质组学以及代谢组学方法。本综述的范围将是蛋白质组学在ACD背景下的应用。这包括突出ACD潜在的分子和细胞机制的相关方面,在经合组织不良结局途径倡议背景下利用这些机制进行检测和寻找生物标志物,以及对新兴蛋白质组靶点(例如在变应原诱导的树突状细胞(DC)激活过程中)的展望。