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系统性硬化症患者血清可溶性 CD163 水平。

Serum levels of soluble CD163 in patients with systemic sclerosis.

机构信息

Department of Dermatology and Plastic Surgery, Faculty of Life Sciences, Kumamoto University, 1-1-1 Honjo, Kumamoto, Japan.

出版信息

Rheumatol Int. 2012 Feb;32(2):403-7. doi: 10.1007/s00296-010-1691-z. Epub 2010 Dec 1.

Abstract

Macrophages may play a role in the pathogenesis of systemic sclerosis (SSc), and CD163-positive M2 macrophages are potentially important source for fibrosis-inducing cytokines. However, no link between M2 macrophages and SSc has been established. The aim is to evaluate the possibility that serum levels of soluble CD163 (sCD163) can be a useful marker for SSc, reflecting M2 activation of macrophages in this disease. Serum sCD163 levels of 43 patients with SSc, 10 patients with scleroderma spectrum disorder (SSD), and 12 healthy controls were measured with specific enzyme-linked immunosorbent assays. SSc patients had significantly higher serum sCD163 levels than healthy controls. The sCD163 levels in SSD patients were higher than healthy controls and lower than SSc patients. Significantly higher right ventricular systolic pressure and lower % DLco levels, and shorter duration of disease were seen in SSc patients with elevated serum sCD163 levels than those with normal levels. These results suggest that sCD163 levels may be increased in proportion to the progression of this disease, indicating the involvement of CD163 in the pathogenesis of SSc. Furthermore, serum sCD163 levels may be a marker of pulmonary hypertension at the early stage in patients with SSc.

摘要

巨噬细胞可能在系统性硬化症(SSc)的发病机制中起作用,CD163 阳性的 M2 巨噬细胞是纤维化诱导细胞因子的潜在重要来源。然而,尚未建立 M2 巨噬细胞与 SSc 之间的联系。本研究旨在评估血清可溶性 CD163(sCD163)水平是否可作为 SSc 的有用标志物,反映该疾病中巨噬细胞的 M2 活化。采用特定的酶联免疫吸附试验测量了 43 例 SSc 患者、10 例硬皮病谱障碍(SSD)患者和 12 名健康对照者的血清 sCD163 水平。SSc 患者的血清 sCD163 水平明显高于健康对照组。SSD 患者的 sCD163 水平高于健康对照组,低于 SSc 患者。血清 sCD163 水平升高的 SSc 患者的右心室收缩压显著升高,%DLco 水平降低,疾病持续时间缩短。这些结果表明,sCD163 水平可能随着疾病的进展而增加,表明 CD163 参与了 SSc 的发病机制。此外,血清 sCD163 水平可能是 SSc 患者早期肺动脉高压的标志物。

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