血管紧张素转化酶。IV.血清活性和溶菌酶浓度的变化作为未经治疗的结节病病程的指标。

C Grönhagen-Riska, O Selroos
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引用次数: 0

摘要

在结节病不同阶段测定的血清血管紧张素转换酶(ACE)活性和溶菌酶(LZM)浓度平均值与临床对疾病状态的评价吻合较好。然而,在检测到改善之前,这两种酶,尤其是LZM,都有所下降。在四分之三的病例中,这些酶的变化与同期临床发展一致。临床观察与LZM波动之间的不一致最常见于活动性、稳定性或非活动性疾病。LZM常在活动性稳定期下降,在非活动性疾病期间不规则波动。在前一阶段,LZM的下降可能反映了肉芽肿性巨噬细胞活性的下降,事实上,在可检测到的改善之前。另一方面,在非活性疾病期间,与疾病过程无关的细胞主导LZM的产生。在稳定型结节病期间,ACE的变化比相应的LZM变化更常与临床发展平行。这可能具有误导性,与LZM相比,由于血清ACE反应延迟,反映了肉芽肿细胞的活性。这种延迟反应也见于结节性红斑。在非活动性结节病期间,稳定的ACE活性表明在试图预测复发时测量的有用性。我们得出结论,ACE可能是结节病的次要特征,而不是巨噬细胞活性的主要功能。
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Angiotensin converting enzyme. IV. Changes in serum activity and in lysozyme concentrations as indicators of the course of untreated sarcoidosis.

The mean values of serum angiotensin-converting enzyme (ACE) activities and lysozyme (LZM) concentrations measured during different phases of sarcoidosis coincided well with the clinical evaluation of the state of the disease. However, both enzymes, especially LZM, decreased before improvement was detected. Changes in these enzymes were in accord with the simultaneous clinical development in three fourths of cases. Incompatibility between clinical observations apnd LZM fluctuations was most frequently seen during active stable or inactive disease. LZM often decreased during the active stable phase and fluctuated irregularly during inactive disease. During the former phase LZM decrements possibly reflect decreasing activity of granulomatous macrophages and, in fact, precede detectable improvement. During inactive disease, on the other hand, cells were not connected with the disease process dominate LZM production. ACE changes paralleled the clinical development more often than corresponding LZM changes during stable sarcoidosis. This may have been misleading and due to a delayed reaction of serum ACE, compared with LZM, inreflecting the activity of granylomatous cells. This delayed reaction was also observed in connection with erythema nodosum. Stable ACE activity during inactive sarcoidosis indicated the usefulness of measurements when trying to predict a relapse. We conclude that ACE may be a secondary feature of sarcoidosis rather than a primary funtion of macrophage activity.

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Circulating immune complexes, free antigen and alpha 1-antitrypsin in levels in sarcoidosis patients. Pulmonary damage associated with gold therapy. A report of two cases. Angiotensin converting enzyme. III. Changes in serum level as an indicator of disease activity in untreated sarcoidosis. Angiotensin converting enzyme. IV. Changes in serum activity and in lysozyme concentrations as indicators of the course of untreated sarcoidosis. Influence of age on bronchial mucociliary transport.
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