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“特发性”隐源性纤维性肺泡炎及合并结缔组织病患者循环免疫复合物的临床意义

Clinical significance of circulating immune complexes in 'lone' cryptogenic fibrosing alveolitis and those with associated connective tissue disorders.

作者信息

Martinet Y, Haslam P L, Turner-Warwick M

出版信息

Clin Allergy. 1984 Sep;14(5):491-7. doi: 10.1111/j.1365-2222.1984.tb02233.x.

Abstract

The clinical, radiographic and physiological features, and progression rates of forty unselected patients with cryptogenic fibrosing alveolitis (CFA) have been studied in relation to serum immune complexes measured by a C1q binding technique. Twenty (50%) had levels greater than normal. Those with associated connective tissue disorders (twenty-four) had a higher frequency of raised C1q binding than those with 'lone' CFA (sixteen) (63% compared to 31%). As observed previously in this group, those with associated disorders also had higher titres of immune complexes. Twelve of thirteen with polyarthritis had immune complexes and a considerably shorter duration of disease compared with those without joint symptoms (P less than 0.01). Several other observations suggest that immune complexes are especially associated with earlier disease. These include a trend towards a younger age and a lesser radiographic profusion score; a shorter duration of symptoms in relation to titres of immune complexes amongst those with raised values (P less than 0.05) and a higher transfer factor coefficient (Kco) (P less than 0.02). The relationship between Kco and the presence of immune complexes was still observed when those with 'lone' CFA were analysed separately. Other clinical features including sex, severity of dyspnoea and lung volumes did not distinguish those with and without complexes, either for the whole group of patients or when those with and without associated connective tissue disorders were analysed separately. Analysis of eighteen patients followed to death showed no correlation between length of survival from first symptoms and immune complexes, neither was there any clear association with corticosteroid responsiveness and immune complexes.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

通过C1q结合技术检测血清免疫复合物,研究了40例未经选择的隐源性纤维性肺泡炎(CFA)患者的临床、影像学和生理学特征以及疾病进展率。20例(50%)患者的免疫复合物水平高于正常。合并结缔组织病的患者(24例)中,C1q结合水平升高的频率高于“单纯性”CFA患者(16例)(分别为63%和31%)。如该组先前观察到的,合并疾病的患者免疫复合物滴度也更高。13例多关节炎患者中有12例存在免疫复合物,与无关节症状的患者相比,疾病持续时间明显更短(P<0.01)。其他一些观察结果表明,免疫复合物尤其与疾病早期相关。这些包括发病年龄较轻的趋势和影像学渗出评分较低;免疫复合物水平升高的患者中,症状持续时间与免疫复合物滴度呈负相关(P<0.05),以及转移因子系数(Kco)较高(P<0.02)。单独分析“单纯性”CFA患者时,仍观察到Kco与免疫复合物存在之间的关系。无论是对整个患者组,还是分别分析合并和未合并结缔组织病的患者,包括性别、呼吸困难严重程度和肺容量在内的其他临床特征均不能区分有无免疫复合物的患者。对18例随访至死亡的患者分析显示,从首次出现症状开始的存活时间与免疫复合物之间无相关性,皮质类固醇反应性与免疫复合物之间也无明显关联。(摘要截短至250字)

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