Molecular Imaging of Pulmonary Fibrosis

Margaret B. Allison, Ciprian Catana, Iris Y. Zhou, Peter Caravan, Sydney B. Montesi
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Abstract

Fibrosing lung diseases affect over 160,000 individuals in the United States alone and can carry a prognosis that is worse than many cancers. Antifibrotic treatments modify only the rate of fibrosis progression, and more effective therapies are urgently needed. Molecular imaging enables visualization of disease pathogenesis in progress. It provides a noninvasive means to monitor and quantify dysregulated molecular fibrotic pathways and shows great promise in aiding the diagnosis and disease activity monitoring of pulmonary fibrosis. Here, we review molecular imaging probes under development for use in pulmonary fibrosis. We provide our opinion on current challenges in translating preclinical molecular imaging probes into clinical successes, as well as future directions for expanding their use in drug development.

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肺纤维化的分子影像学
仅在美国就有超过 16 万人患有肺纤维化疾病,其预后可能比许多癌症还糟糕。抗纤维化治疗只能改变纤维化的进展速度,因此迫切需要更有效的疗法。分子成像技术可将疾病的发病过程可视化。它为监测和量化失调的分子纤维化通路提供了一种无创手段,在帮助诊断和监测肺纤维化的疾病活动方面大有可为。在此,我们回顾了正在开发的用于肺纤维化的分子成像探针。我们就目前将临床前分子成像探针转化为临床成功所面临的挑战,以及扩大其在药物开发中的应用的未来方向提出了自己的看法。
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