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高肾树突状细胞 C 型凝集素(DC-SIGN)细胞密度与 IgA 肾病患者严重肾脏病变和不良预后相关。

High renal DC-SIGN cell density is associated with severe renal lesions and poor prognosis in patients with immunoglobulin A nephropathy.

机构信息

Division of Nephrology, Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, China.

出版信息

Histopathology. 2019 Apr;74(5):744-758. doi: 10.1111/his.13803. Epub 2019 Mar 2.

Abstract

BACKGROUND AND AIMS

In this observational cohort study, we assessed the prognostic value of DC-SIGN cells in the pathogenesis and progression of IgA nephropathy (IgAN).

METHODS AND RESULTS

A total of 139 adult IgAN patients were enrolled into this study from June 2009 to June 2010. We characterised DC-SIGN cells by immunohistochemistry or immunofluorescence in renal biopsy tissue. Correlations between the DC-SIGN, intercellular adhesion molecule 3 (ICAM-3), CD4 and CD8 were evaluated. Patients were classified into the DC-SIGN and DC-SIGN groups. Depending on an average of 100-month follow-up, the predictive value of DC-SIGN cells in IgAN progression was analysed. DC-SIGN cells were found frequently in IgAN kidneys while rarely observed in normal kidneys, and almost all DC-SIGN cells expressed MHC-II. We also found that DC-SIGN cells were adjacent to ICAM-3-positive CD4 and CD8 lymphocytes. The density of DC-SIGN cells was positively and linearly correlated with the density of ICAM-3 cells, CD4 cells and CD8 cells in renal biopsy tissues. In the DC-SIGN group, the degree of renal lesion and inflammatory cell infiltration was more severe compared to the DC-SIGN group. Patients in the DC-SIGN group also had increased incidences of deteriorating renal function during the follow up compared to patients in the DC-SIGN group.

CONCLUSIONS

DC-SIGN cells probably served as a potential contributor to exacerbate local inflammatory response. The density of DC-SIGN cells was associated with the severity of renal lesions of the patients. High renal DC-SIGN cell density might be used as a predictor of poor prognosis in patients with IgAN.

摘要

背景与目的

在这项观察性队列研究中,我们评估了 DC-SIGN 细胞在 IgA 肾病(IgAN)发病机制和进展中的预后价值。

方法和结果

我们共纳入 139 例成人 IgAN 患者,他们均于 2009 年 6 月至 2010 年 6 月在我院接受治疗。我们通过免疫组化或免疫荧光法在肾活检组织中对 DC-SIGN 细胞进行了特征描述。评估了 DC-SIGN、细胞间黏附分子 3(ICAM-3)、CD4 和 CD8 之间的相关性。根据平均 100 个月的随访结果,分析了 DC-SIGN 细胞在 IgAN 进展中的预测价值。结果发现,DC-SIGN 细胞在 IgAN 肾脏中频繁出现,而在正常肾脏中很少观察到,几乎所有的 DC-SIGN 细胞都表达 MHC-II。我们还发现,DC-SIGN 细胞与 ICAM-3 阳性的 CD4 和 CD8 淋巴细胞相邻。肾活检组织中 DC-SIGN 细胞的密度与 ICAM-3 细胞、CD4 细胞和 CD8 细胞的密度呈正线性相关。在 DC-SIGN 组中,与 DC-SIGN 组相比,患者的肾脏病变程度和炎症细胞浸润更为严重。与 DC-SIGN 组相比,在随访期间,DC-SIGN 组患者肾功能恶化的发生率也更高。

结论

DC-SIGN 细胞可能是加剧局部炎症反应的潜在因素。DC-SIGN 细胞的密度与患者肾脏病变的严重程度有关。肾 DC-SIGN 细胞密度高可能可作为 IgAN 患者预后不良的预测因子。

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