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外周血免疫表型分析有助于了解特发性肉芽肿性多血管炎的病因吗?

Is peripheral blood immunophenotyping useful to understand the etiology of Idiopathic Granulomatous?

机构信息

Istanbul Teaching and Research Hospital, Department of General Surgery, Turkey.

Istanbul Teaching and Research Hospital, Department of General Surgery, Turkey.

出版信息

Hum Immunol. 2023 May-Jul;84(5-7):315-319. doi: 10.1016/j.humimm.2023.05.001. Epub 2023 May 16.

Abstract

BACKGROUND

The etiology of idiopathic granulomatous mastitis (IGM) has not been clearly established. However, autoimmunity has recently become popular in etiopathogenesis. We aimed to investigate the immunophenotyping of immune cells to help clarify the etiopathogenesis of the disease.

METHODS

Patients with IGM and healthy volunteers were included in the study. Patients were divided into active and remission groups based on their disease status. The ratios of total T cells, helper T cells, cytotoxic T cells, natural killer cells, regulatory T cells, and monocyte subtypes were measured using flow cytometry. In addition, age, complete blood count for leukocyte, lymphocyte, neutrophil, and eosinophil counts, and the smoking status of all volunteers were evaluated.

RESULTS

A total of 33 volunteers, including 11 patients with active IGM, 10 patients with remission IGM, and 12 healthy volunteers, were included in the study. The neutrophil, eosinophil, neutrophil/lymphocyte, and non-classical monocyte values were significantly higher in IGM patients than in healthy volunteers. Additionally, the CD4 CD25 CD127 regulatory T cell was significantly lower in IGM patients than in healthy volunteers. Furthermore, neutrophil, neutrophil/lymphocyte ratio, CD4 CD25 CD127 regulatory T cells, and non-classical monocytes showed significant differences when IGM patients were divided into active and remission groups. IGM patients had higher smoking rates, but this was not statistically significant.

CONCLUSION

The changes in many cell types evaluated in our study were similar to the cell profiles of some autoimmune diseases. This could provide minor evidence to suggest that IGM is an autoimmune granulomatous disease with a local course.

摘要

背景

特发性肉芽肿性乳腺炎(IGM)的病因尚未明确。然而,自身免疫在发病机制中最近变得流行。我们旨在研究免疫细胞的免疫表型,以帮助阐明疾病的发病机制。

方法

本研究纳入了 IGM 患者和健康志愿者。根据疾病状态将患者分为活动期和缓解期。使用流式细胞术测量总 T 细胞、辅助 T 细胞、细胞毒性 T 细胞、自然杀伤细胞、调节性 T 细胞和单核细胞亚型的比例。此外,评估了所有志愿者的年龄、白细胞全血细胞计数、淋巴细胞、中性粒细胞和嗜酸性粒细胞计数以及吸烟状况。

结果

共有 33 名志愿者,包括 11 名活动性 IGM 患者、10 名缓解性 IGM 患者和 12 名健康志愿者,纳入本研究。与健康志愿者相比,IGM 患者的中性粒细胞、嗜酸性粒细胞、中性粒细胞/淋巴细胞和非经典单核细胞值明显更高。此外,IGM 患者的 CD4 CD25 CD127 调节性 T 细胞明显低于健康志愿者。此外,当 IGM 患者分为活动期和缓解期时,中性粒细胞、中性粒细胞/淋巴细胞比值、CD4 CD25 CD127 调节性 T 细胞和非经典单核细胞显示出显著差异。IGM 患者的吸烟率较高,但无统计学意义。

结论

我们研究中评估的许多细胞类型的变化与某些自身免疫性疾病的细胞谱相似。这可能提供了一些证据,表明 IGM 是一种具有局部病程的自身免疫性肉芽肿性疾病。

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