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特发性肺纤维化:新型治疗方法的病理生物学。

Idiopathic pulmonary fibrosis: pathobiology of novel approaches to treatment.

机构信息

Interstitial Lung Disease Unit, Royal Brompton Hospital, London, UK.

出版信息

Clin Chest Med. 2012 Mar;33(1):69-83. doi: 10.1016/j.ccm.2011.11.002. Epub 2011 Dec 28.

Abstract

Idiopathic pulmonary fibrosis (IPF) is a progressive disease of unknown cause that conveys a dismal prognosis. In the United States there are currently no licensed therapies for treatment of IPF. The development of effective IPF clinical trials networks across the United States and Europe, however, has led to key developments in the treatment of IPF. Advances in understanding of the pathogenetic processes involved in the development of pulmonary fibrosis have led to novel therapeutic targets. These developments offer hope that there may, in the near future, be therapeutic options available for treatment of this devastating disease.

摘要

特发性肺纤维化(IPF)是一种病因不明的进行性疾病,预后不良。目前,美国还没有针对 IPF 的许可疗法。然而,美国和欧洲有效的 IPF 临床试验网络的发展,导致了 IPF 治疗方面的关键进展。对肺纤维化发展过程中涉及的发病机制的深入了解,为新的治疗靶点提供了依据。这些进展带来了希望,即可能在不久的将来,为治疗这种毁灭性疾病提供治疗选择。

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