抗纤维化药物研发进展
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国家自然科学基金(82270679, 82104257).


Research progress in anti-fibrotic drugs
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    摘要:

    纤维化是一种以损伤和修复平衡失调导致的细胞外基质过度沉积为特征的病理状态。它可累及包括心、肺、肝、肾和胰腺在内的多个器官,其进程通常较为缓慢且难以逆转,严重影响器官功能。在工业化国家,因纤维化导致的死亡率高达45%,造成了巨大的医疗负担,亟须能够逆转或延缓纤维化进展的药物。近年来,对不同器官纤维化发病机制的研究取得了显著进展,针对纤维化的药物也正在积极研发中。本文简要综述了目前用于治疗纤维化的已上市药物、临床试验阶段的药物进展现状。

    Abstract:

    Fibrosis is a pathological condition characterized by the excessive deposition of extracellular matrix due to the imbalance between injury and repair. It can affect multiple organs, including the heart, lungs, liver, kidneys, and pancreas. The progression of fibrosis is usually slow and difficult to reverse, and it can severely impair organ functions. In industrialized countries, deaths caused by fibrosis account for up to 45%, resulting in a tremendous disease burden. Thus, there is an urgent need for drugs that can reverse or delay the progression of fibrosis. In recent years, remarkable progress has been made in the research on the pathogenesis of fibrosis in different organs, and relevant drugs targeting fibrosis are also under active development. This article briefly summarizes the drugs currently marketed and drugs at the clinical trial stage for treating fibrosis.

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  • 收稿日期:2025-05-28
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  • 在线发布日期: 2025-10-25
  • 出版日期: 2025-10-20
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