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[镍的耐受性诱导。从动物模型到人类]

[Tolerance induction towards nickel. From animal model to humans].

作者信息

Artik S, Gleichmann E, Ruzicka T

机构信息

Institut für umweltmedizinische Forschung an der Heinrich-Heine-Universität Düsseldorf gGmbH, Abteilung für Allergologie und Immunologie, Universitätshautklinik, Heinrich-Heine-Universität Düsseldorf

出版信息

Hautarzt. 2004 Nov;55(11):1052-9. doi: 10.1007/s00105-004-0815-3.

DOI:10.1007/s00105-004-0815-3
PMID:15365644
Abstract

Nickel is the most common contact allergen in humans. Until recently, many questions concerning tolerance mechanisms to nickel were unresolved. Besides human ex vivo, intervention and observation studies, the establishment of a reproducible mouse model has contributed to the analysis of these mechanisms. A more detailed understanding of the pathogenesis of nickel allergy and tolerance towards nickel by investigations in an animal model and in human studies is a prerequisite for developing specific prevention and therapy of nickel allergy. With this article, we provide a review of the investigations concerning nickel allergy and give perspectives towards oral tolerance induction to nickel in the animal model and in humans.

摘要

镍是人类最常见的接触性过敏原。直到最近,许多关于镍耐受机制的问题仍未得到解决。除了人体离体、干预和观察研究外,可重复的小鼠模型的建立有助于对这些机制进行分析。通过在动物模型和人体研究中的调查,更详细地了解镍过敏的发病机制和对镍的耐受性,是开发镍过敏特异性预防和治疗方法的先决条件。在本文中,我们对有关镍过敏的研究进行了综述,并展望了在动物模型和人体中诱导对镍的口服耐受性。

相似文献

1
[Tolerance induction towards nickel. From animal model to humans].[镍的耐受性诱导。从动物模型到人类]
Hautarzt. 2004 Nov;55(11):1052-9. doi: 10.1007/s00105-004-0815-3.
2
Characterization of skin sensitizing chemicals: a lesson learnt from nickel allergy.皮肤致敏化学物质的特性:从镍过敏中吸取的教训。
J Immunotoxicol. 2011 Jan-Mar;8(1):1-2. doi: 10.3109/1547691X.2010.531298. Epub 2010 Nov 11.
3
Allergy to nickel: first results on patients administered with an oral hyposensitization therapy.镍过敏:接受口服减敏疗法患者的初步结果。
Int J Immunopathol Pharmacol. 2009 Jul-Sep;22(3):837-40. doi: 10.1177/039463200902200330.
4
Nickel and Skin: From Allergy to Autoimmunity.镍与皮肤:从过敏到自身免疫。
Endocr Metab Immune Disord Drug Targets. 2020;20(7):1032-1040. doi: 10.2174/1871530320666191231115437.
5
Molecular profiling of contact dermatitis skin identifies allergen-dependent differences in immune response.接触性皮炎皮肤的分子谱分析确定了免疫反应中过敏原依赖性的差异。
J Allergy Clin Immunol. 2014 Aug;134(2):362-72. doi: 10.1016/j.jaci.2014.03.009. Epub 2014 Apr 25.
6
Nickel allergy versus nickel tolerance: can oral uptake of nickel protect from sensitization?镍过敏与镍耐受性:口服镍能预防致敏吗?
J Environ Monit. 2004 Dec;6(12):146N-150N.
7
Wavelength dependency for UVA-induced suppression of recall immunity in humans.长波紫外线对人体回忆性免疫抑制的波长依赖性。
J Dermatol Sci. 2010 Sep;59(3):192-7. doi: 10.1016/j.jdermsci.2010.07.005. Epub 2010 Aug 9.
8
The immunology of nickel-induced allergic contact dermatitis.镍诱导的变应性接触性皮炎的免疫学
Asian Pac J Allergy Immunol. 1995 Dec;13(2):173-81.
9
Nickel Allergy of the Skin and Beyond.皮肤及其他部位的镍过敏
Endocr Metab Immune Disord Drug Targets. 2020;20(7):1003-1009. doi: 10.2174/1871530320666200228124453.
10
[Can allergy to nickel be diminished by induction of "tolerance"?].[能否通过诱导“耐受”来减轻对镍的过敏反应?]
Ann Dermatol Venereol. 1999 Jun-Jul;126(6-7):486-8.

本文引用的文献

1
Infectious nickel tolerance: a reciprocal interplay of tolerogenic APCs and T suppressor cells that is driven by immunization.传染性镍耐受性:一种由免疫驱动的耐受性抗原呈递细胞和T抑制细胞之间的相互作用。
J Immunol. 2003 Sep 15;171(6):2863-72. doi: 10.4049/jimmunol.171.6.2863.
2
T cell receptor transfection shows non-HLA-restricted recognition of nickel by CD8+ human T cells to be mediated by alphabeta T cell receptors.T细胞受体转染显示,CD8⁺人T细胞对镍的非HLA限制识别由αβ T细胞受体介导。
J Invest Dermatol. 2003 Sep;121(3):496-501. doi: 10.1046/j.1523-1747.2003.12405.x.
3
ELISpot: a new tool for the detection of nickel sensitization.
酶联免疫斑点技术:一种检测镍致敏的新工具。
Clin Exp Allergy. 2003 Jul;33(7):992-8. doi: 10.1046/j.1365-2222.2003.01700.x.
4
A new type of metal recognition by human T cells: contact residues for peptide-independent bridging of T cell receptor and major histocompatibility complex by nickel.人类T细胞识别金属的新方式:镍介导的T细胞受体与主要组织相容性复合体非肽依赖性桥接的接触残基
J Exp Med. 2003 May 19;197(10):1345-53. doi: 10.1084/jem.20030121.
5
Components of the ligand for a Ni++ reactive human T cell clone.一种与Ni++反应的人T细胞克隆的配体成分。
J Exp Med. 2003 Mar 3;197(5):567-74. doi: 10.1084/jem.20021762.
6
Nickel sensitization in adolescents and association with ear piercing, use of dental braces and hand eczema. The Odense Adolescence Cohort Study on Atopic Diseases and Dermatitis (TOACS).青少年中的镍致敏及其与穿耳洞、使用牙套和手部湿疹的关联。欧登塞青少年特应性疾病和皮炎队列研究(TOACS)。
Acta Derm Venereol. 2002;82(5):359-64. doi: 10.1080/000155502320624096.
7
Cytokine production in nickel-sensitized individuals analysed with enzyme-linked immunospot assay: possible implication for diagnosis.用酶联免疫斑点法分析镍致敏个体中的细胞因子产生:对诊断的可能意义
Br J Dermatol. 2002 Sep;147(3):442-9. doi: 10.1046/j.1365-2133.2002.04850.x.
8
Decrease in nickel sensitization in a Danish schoolgirl population with ears pierced after implementation of a nickel-exposure regulation.在丹麦实施镍暴露规定后, pierced ears 的女学生群体中镍致敏率降低。 (这里 pierced ears 不太明确准确意思,可能是“穿耳洞的”之类,你可根据实际情况调整完善表述)
Br J Dermatol. 2002 Apr;146(4):636-42. doi: 10.1046/j.1365-2133.2002.04666.x.
9
Environmental nickel pollution: does it protect against nickel allergy?环境镍污染:它能预防镍过敏吗?
J Am Acad Dermatol. 2002 Mar;46(3):460-2. doi: 10.1067/mjd.2002.120443.
10
Tolerance to nickel: oral nickel administration induces a high frequency of anergic T cells with persistent suppressor activity.对镍的耐受性:口服镍会诱导产生高频率的具有持续抑制活性的无反应性T细胞。
J Immunol. 2001 Dec 15;167(12):6794-803. doi: 10.4049/jimmunol.167.12.6794.