弹性假性黄瘤患者伴有Th1极性的t细胞相关皮肤炎症发作

Q3 Medicine
Skin health and disease Pub Date : 2024-11-26 eCollection Date: 2024-12-01 DOI:10.1002/ski2.430
Samuel Rocour, Emeline Vinatier, Céline Fassot, Jonathan Dauvé, Agnès Toutain, Sabrina Fronteau, Marine Monnier, Laurence Preisser, Anne Croué, Olivier Le Saux, Alain Morel, Yves Delneste, Ludovic Martin
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引用次数: 0

摘要

弹性假性黄瘤(PXE)是一种以富含弹性纤维的组织异位钙化为特征的遗传性疾病(OMIM 264800)。迄今为止,PXE被认为是一种与促钙化因子和抗钙化因子失衡有关的代谢性疾病。我们在法国PXE参考中心多次听到PXE皮肤病变散发性红斑发作的投诉。然而,这种罕见的临床表现从未被广泛研究过。我们有机会调查一位13岁的患者,他的PXE病变出现红斑性发作。我们进行这项工作是为了确定他的病变涉及哪种类型的炎症。对最近发生的腹股沟红斑性PXE病变进行了切口皮肤活检,并送去进行组织学和转录组学分析。将结果与另一名年轻PXE患者的非红斑PXE影响皮肤活检进行比较。组织学检查显示血管周围t细胞浸润Th1极性,RNAseq和RT-qPCR分析显示细胞毒性标志物表达升高。Th17和Th2标记物没有增加。我们的发现支持了先前关于PXE发展中可能存在炎症成分的证据。th1依赖性炎症是作为一种主动过程参与病理还是作为一种加重因素需要进一步研究。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
T-cell-related skin inflammatory flareups with Th1 polarity in a patient with pseudoxanthoma elasticum.

Pseudoxanthoma elasticum (PXE) is a genetic disorder characterized by ectopic calcification of tissues rich in elastic fibres (OMIM 264800). To date, PXE is considered a metabolic disease linked to an imbalance between pro- and anti-calcifying factors. The occurrence of sporadic erythematous flareups of PXE skin lesions is a complaint that we heard about on several occasions at the French PXE reference centre. However, this rare clinical aspect had never been extensively studied. We have had the opportunity to investigate a 13-year-old patient experiencing an erythematous flareup of his PXE lesions. We conducted this work to identify what type of inflammation was implicated in his lesions. An incisional skin biopsy on a recent erythematous inguinal PXE lesion was performed and sent for histological and transcriptomic analyses. The findings were compared to a non-erythematous PXE-affected skin biopsy obtained from another young PXE patient. Histological examination revealed perivascular T-cell infiltrates with Th1 polarity and elevated expression of cytotoxicity markers in RNAseq and RT-qPCR analyses. There was no increase in Th17 or Th2 markers. Our findings support the previous evidence of a possible inflammatory component in the development of PXE. Whether Th1-dependent inflammation contributes to the pathology as an active process or is an aggravating factor requires further investigations.

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CiteScore
1.70
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