Pulmonary sarcoidosis during interferon therapy: a rare or underestimated event?

Antonio Salvio, Mauro Mormile, Francesco Giannattasio, Maria Varriale, Tito d'Errico, Brigida Balzano, Pierluigi Carratù, Giovanni Tufano, Mario Visconti
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Abstract

Interferon (IFN)-alpha with or without ribavirin is the treatment of choice for patients with chronic HCV-related hepatitis. Cough and dyspnea during IFN therapy are often regarded as a side effect and not as a possible sign of the onset of a pulmonary interstitial disease. It may therefore be claimed that the likelihood that patients treated with IFN develop sarcoidosis is being underestimated. Although they are not conventionally classified as etiopathologic agents of sarcoidosis, the IFNs have been proven to be capable of triggering macrophages and of promoting the expression of class II HLA antigens. It is therefore possible that IFN-alpha treatment could trigger macrophages and promote the polarization of the immune response towards Th1 in the presence of particular susceptibility conditions, thus starting the series of events that lead to the onset of sarcoidosis. We describe a case of pulmonary sarcoidosis in a 33-year-old patient treated with IFN-alpha2b and ribavirin for chronic HCV-related hepatitis after 6 months of therapy. The case we report here brings forth the issue of a possible underestimation of the real incidence of sarcoidosis during IFN therapy and highlights the need for more attention to and a more careful evaluation of respiratory symptoms manifesting in treated patients.

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干扰素治疗期间肺结节病:罕见事件还是低估事件?
干扰素(IFN)- α联合或不联合利巴韦林是慢性丙型肝炎相关肝炎患者的治疗选择。在IFN治疗期间,咳嗽和呼吸困难通常被认为是一种副作用,而不是肺间质性疾病发病的可能迹象。因此,用干扰素治疗的患者发生结节病的可能性被低估了。虽然它们通常不被归类为结节病的致病因子,但ifn已被证明能够触发巨噬细胞并促进II类HLA抗原的表达。因此,在特定易感条件下,ifn - α治疗可能会触发巨噬细胞,促进对Th1的免疫反应极化,从而启动一系列导致结节病发病的事件。我们描述了一例33岁的慢性hcv相关肝炎患者,在接受IFN-alpha2b和利巴韦林治疗6个月后出现肺结节病。我们在此报告的病例提出了在IFN治疗期间可能低估结节病真实发病率的问题,并强调需要更多地关注和更仔细地评估治疗患者的呼吸道症状。
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