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金属过敏的免疫机制和镍特异性 TCR-pMHC 界面。

Immunological Mechanisms of Metal Allergies and the Nickel-Specific TCR-pMHC Interface.

机构信息

Department for Chemicals and Product Safety, Federal Institute for Risk Assessment, Max-Dohrn-Straße 8-10, 10589 Berlin, Germany.

Institute of Pharmacy, Freie Universität Berlin, Königin-Luise-Straße 2, 14195 Berlin, Germany.

出版信息

Int J Environ Res Public Health. 2021 Oct 15;18(20):10867. doi: 10.3390/ijerph182010867.

Abstract

Besides having physiological functions and general toxic effects, many metal ions can cause allergic reactions in humans. We here review the immune events involved in the mediation of metal allergies. We focus on nickel (Ni), cobalt (Co) and palladium (Pd), because these allergens are among the most prevalent sensitizers (Ni, Co) and immediate neighbors in the periodic table of the chemical elements. Co-sensitization between Ni and the other two metals is frequent while the knowledge on a possible immunological cross-reactivity using in vivo and in vitro approaches remains limited. At the center of an allergic reaction lies the capability of a metal allergen to form T cell epitopes that are recognized by specific T cell receptors (TCR). Technological advances such as activation-induced marker assays and TCR high-throughput sequencing recently provided new insights into the interaction of Ni with the αβ TCR-peptide-major histocompatibility complex (pMHC) interface. Ni functionally binds to the TCR gene segment TRAV9-2 or a histidine in the complementarity determining region 3 (CDR3), the main antigen binding region. Thus, we overview known, newly identified and hypothesized mechanisms of metal-specific T cell activation and discuss current knowledge on cross-reactivity.

摘要

除了具有生理功能和一般毒性作用外,许多金属离子也会引起人类的过敏反应。我们在这里回顾了介导金属过敏的免疫事件。我们重点关注镍(Ni)、钴(Co)和钯(Pd),因为这些变应原是最常见的致敏原(Ni、Co),也是化学元素周期表中的近邻。Ni 与另外两种金属之间的共致敏现象很常见,而使用体内和体外方法研究可能的免疫交叉反应的知识仍然有限。过敏反应的核心是金属变应原形成 T 细胞表位的能力,这些表位被特定的 T 细胞受体(TCR)识别。激活诱导标记物测定和 TCR 高通量测序等技术的进步最近为 Ni 与 αβ TCR-肽-主要组织相容性复合体(pMHC)界面的相互作用提供了新的见解。Ni 可与 TCR 基因片段 TRAV9-2 或互补决定区 3(CDR3)中的组氨酸发生功能结合,这是主要的抗原结合区域。因此,我们概述了已知的、新确定的和假设的金属特异性 T 细胞激活机制,并讨论了目前关于交叉反应的知识。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b6f7/8535423/444d508e4f0f/ijerph-18-10867-g001.jpg

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