结节病中的c反应蛋白。

Acta medica Iugoslavica Pub Date : 1991-01-01
T Peroś-Golubicić
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引用次数: 0

摘要

结节病的特点是肉芽肿形成,巨噬细胞是最重要的组成部分。结节病中活化的巨噬细胞产生白细胞介素-1 (II-1)。众所周知,除其他功能外,白细胞介素-1还能刺激肝脏产生c反应蛋白。因此,我们前瞻性地测量了17例活动性肺结节病患者、10例病因不明的其他慢性间质性肺疾病患者、11例活动性肺结核患者和10名健康志愿者的血清c反应蛋白。采用酶免疫扩散法检测血清c反应蛋白。活动性结节病13例血清c反应蛋白阴性,4例阳性。其他肺间质性疾病7例阴性,3例阳性。10例痰阳性肺结核患者c反应蛋白分析呈阳性。所有健康对照组的c反应蛋白检测结果均为阴性。结节病组与肺结核组血清c反应蛋白比较,组间差异有统计学意义(p < 0.01),其他肺间质性疾病组与肺结核组间差异有统计学意义(p < 0.01)。在这方面,血清c反应蛋白的测量对于结节病和其他病因不明的慢性间质性肺疾病与结核病和其他已知可引起急性期反应的疾病的区分是有价值的。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
C-reactive protein in sarcoidosis.

Sarcoidosis is characterized by granuloma formation, the macrophage being the most important building block. The activated macrophage in sarcoidosis produces interleukin-1 (II-1). It is well known that interleukin-1, among other functions, stimulates the hepatic production of C-reactive protein. We therefore prospectively measured the serum C-reactive protein in 17 patients with active pulmonary sarcoidosis, 10 patients with other chronic interstitial lung diseases of unknown etiology, 11 patients with active lung tuberculosis, and 10 healthy volunteers. Serum C-reactive protein was assayed by enzymoimmunodiffusion test. The serum C-reactive protein was negative in 13 patients suffering from active sarcoidosis and positive in four. Patients with other interstitial lung diseases had negative results in 7 and positive in 3 cases. The analyses of C-reactive protein in patients with sputum positive lung tuberculosis were positive in 10 cases. All the healthy controls had negative C-reactive protein measurements. The difference between the groups was statistically significant when sarcoidosis and tuberculosis serum C-reactive protein measurements were compared (p less than 0.01), as well as the difference between the group of other interstitial lung diseases and tuberculosis (p less than 0.01). In this respect, the measurements of serum C-reactive protein are valuable in the differentiation of sarcoidosis and other chronic interstitial lung diseases of unknown etiology from tuberculosis and other diseases which are known to induce an acute phase response.

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