Păunescu E, Burnea D, Zaharescu C, Stoinescu M, Algeorge G, Petre A, Corlan E, Smărăndache M, Dănălache-Dumitrescu M, Jienescu Z, Oprişiu G
Rev Ig Bacteriol Virusol Parazitol Epidemiol Pneumoftiziol Pneumoftiziol. 1982 Apr-Jun;31(2):141-50.
Seven patients with advanced forms of mediastino-pulmonary sarcoidosis (involvement of the pulmonary parenchyma, and restrictive respiratory syndrome), confirmed by histopathologic investigation, have been treated with a new SV-rifamycin derivative, 1246-EH, or "Reprimum" without any other association. Reprimun was given in daily doses of 10 mg/kg of body weight for a period of two weeks, then, for another 4-5 weeks, the drugs was given intermittently in doses of 15 mg/kg of body weight twice weekly. Between two cycles of therapy a period of 14 days was free of drug administration. In all patients the treatment with the new derivative was well tolerated. The treatment was not followed by adrenal deficiencies, neither was noted obesity, bone decalcification, gastric ulcers, etc., which are commonly associated with prolonged corticoid therapy. The treatment with "Reprimun" efficient for all patients. A clear clinical and X-ray improvement was noted after the first three months of treatment with the new drug. Respiratory function, as well as clinical and radiological signs improved, the serum immunologic parameters, and the biochemical ones were also significantly improved (Ig, C3 total serum proteins and gammaglobulins). All parameters which were tested were finally improved and became normal. In only two of the seven patients the radiological aspects of the lung suggested the presence of sequellae at the end of the treatment. In these two patients there was a persistant reduction in the respiratory volume, as well as a discret hypoxemia. However, both these patients had a more advanced form of the disease, with extensive pulmonary fibrosis, and in these cases prolonged corticoid therapy which had previously been applied had failed. Reprimun had an immunological-modulatory effect in all patients, resulting in normal levels of IgG, IgA, and C3 in the first three months of therapy. There was a direct correlation between the normalization of immunological indicators and the good evolution of the diseases, a fact which suggests once again the existence of some immune mechanisms involved in the maintenance of sarcoidosis.
七名经组织病理学检查确诊为晚期纵隔-肺结节病(累及肺实质并伴有限制性呼吸综合征)的患者,接受了一种新的SV-利福霉素衍生物1246-EH或“Reprimum”的治疗,未联合使用其他药物。Reprimun的给药剂量为每日10毫克/千克体重,持续两周,然后在接下来的4至5周内,以15毫克/千克体重的剂量每周两次间歇给药。两个治疗周期之间有14天的停药期。所有患者对这种新衍生物的治疗耐受性良好。治疗后未出现肾上腺功能减退,也未发现肥胖、骨质脱钙、胃溃疡等通常与长期使用皮质类固醇治疗相关的情况。“Reprimun”治疗对所有患者均有效。使用新药治疗的前三个月后,临床和X线检查有明显改善。呼吸功能以及临床和放射学体征均有改善,血清免疫学参数和生化参数也显著改善(免疫球蛋白、C3、总血清蛋白和γ球蛋白)。所有检测参数最终均得到改善并恢复正常。七名患者中只有两名在治疗结束时肺部的放射学表现提示有后遗症。在这两名患者中,呼吸量持续减少,并有轻度低氧血症。然而,这两名患者的病情都更为严重,存在广泛的肺纤维化,并且此前应用的长期皮质类固醇治疗均告失败。Reprimun对所有患者都有免疫调节作用,在治疗的前三个月使IgG、IgA和C3水平恢复正常。免疫指标的正常化与疾病的良好转归之间存在直接相关性,这一事实再次表明存在一些参与结节病维持的免疫机制。