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SOX9 和 CD34 在斑秃中的免疫组化表达价值。

The value of immunohistochemical expression of SOX9 and CD34 in alopecia areata.

机构信息

Dermatology and Andrology Department, Faculty of Medicine, Menoufia University, Shebeen El-Kom, Egypt.

Pathology Department, Faculty of Medicine, Menoufia University, Shebeen El-Kom, Egypt.

出版信息

J Immunoassay Immunochem. 2024 Sep 2;45(5):452-466. doi: 10.1080/15321819.2024.2383676. Epub 2024 Jul 23.

Abstract

BACKGROUND

Alopecia areata (AA), an immune-mediated disorder, is marked by temporary, nonscarring hair loss. The bulge area is protected from immune attacks by immune privilege; however, recent studies demonstrated immune cells infiltrating the bulge area.

OBJECTIVE

This study aims to investigate the immunohistochemical expression of the sex-determining region Y-box 9 (SOX9) and cluster of differentiation 34 (CD34) in AA patients as markers of hair follicle stem cells (HFSCs) and progenitor cells, respectively.

METHODS

Immunohistochemical staining of SOX9 and CD34 was applied on skin samples of 20 AA patients and 20 healthy controls.

RESULTS

SOX9 and CD34 were significantly lower in lesional samples of cases compared to perilesional and control skin biopsies. Furthermore, SOX9 level was negatively correlated with the severity of alopecia tool score (SALT score) among the studied AA patients. Moreover, lowered SOX9 expression was present in patients with recurrent attacks.

CONCLUSIONS

The significant reduction of stem cell markers (SOX9 and CD34) in our studied AA cases signifies the pathological affection of HFSCs and their progeny in AA. This is thought to cause a loss of competence in generating new hair in some AA cases, which needs to be validated in further research.

LIMITATIONS OF THE STUDY

This study has a small sample size.

摘要

背景

斑秃(AA)是一种免疫介导的疾病,其特征是暂时性、非瘢痕性脱发。隆突区受到免疫特权的保护,免受免疫攻击;然而,最近的研究表明免疫细胞浸润隆突区。

目的

本研究旨在探讨性别决定区 Y 框 9(SOX9)和分化群 34(CD34)在 AA 患者中的免疫组织化学表达,分别作为毛囊干细胞(HFSCs)和祖细胞的标志物。

方法

对 20 例 AA 患者和 20 例健康对照的皮肤样本进行 SOX9 和 CD34 的免疫组织化学染色。

结果

与病变周围和对照皮肤活检相比,病例的病变样本中 SOX9 和 CD34 明显降低。此外,SOX9 水平与研究中的 AA 患者的脱发严重程度工具评分(SALT 评分)呈负相关。此外,在复发性发作的患者中存在降低的 SOX9 表达。

结论

我们研究的 AA 病例中干细胞标志物(SOX9 和 CD34)的显著减少表明 HFSCs 及其祖细胞在 AA 中的病理影响。这被认为导致一些 AA 病例中产生新毛发的能力丧失,这需要在进一步的研究中得到验证。

局限性

本研究样本量较小。

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