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

机译:循环免疫复合物在“孤岛”隐源性纤维化肺泡炎和伴有结缔组织疾病的患者中的临床意义

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SummaryThe 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<0.0l).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<0.05) and a higher transfer factor coefficient (Kco)(P<0.02). The relationship between Kco and the presence of immune complexes was still observed when those with ‘lone’ CKA 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.These studies suggest that measurement of serum C1q binding does not contribute substantially to the management of individual patients with cryptogenic fibrosing a
机译:摘要已研究了 40 例未经选择的隐源性纤维化肺泡炎 (CFA) 患者的临床、影像学和生理学特征以及进展率与通过 C1q 结合技术测量的血清免疫复合物的关系。20例(50%)的水平高于正常水平。患有相关结缔组织疾病的患者(24 例)的 C1q 结合频率高于“孤独”CFA(16 例)(63% 对 31%)。正如之前在该组中观察到的那样,患有相关疾病的人也具有较高的免疫复合物滴度。13 例多发性关节炎患者中有 12 例具有免疫复合物,与没有关节症状的患者相比,病程明显缩短 (P<0.0l)。其他几项观察表明,免疫复合物与早期疾病特别相关。这些因素包括年龄更年轻和影像学丰满评分较低的趋势;在值升高(P<0.05)和转移因子系数(Kco)较高的患者中,与免疫复合物滴度相关的症状持续时间较短(P<0.02)。当单独分析那些具有“孤独”CKA的人时,仍然观察到Kco与免疫复合物存在之间的关系。其他临床特征,包括性别。呼吸困难的严重程度和肺容积不能区分有和没有复合物的患者,无论是对于整个患者组,还是当有和没有相关结缔组织疾病的患者分别进行分析时。对 18 名随访至死亡的患者的分析显示,从最初症状开始的生存时间与免疫复合物之间没有相关性,与皮质类固醇反应性和免疫复合物之间也没有任何明确的关联。这些研究表明,血清 C1q 结合的测量对个体隐源性纤维化 a 患者的管理没有实质性贡献

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