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中国临床药理学与治疗学 ›› 2024, Vol. 29 ›› Issue (5): 583-589.doi: 10.12092/j.issn.1009-2501.2024.05.014

• 综述与讲座 • 上一篇    下一篇

CXC趋化因子及其受体与肺纤维化的研究进展

陈凤1,李龙2,王洁1,刘胜菲1   

  1. 1兰州大学第一临床医学院,兰州  730000,甘肃;2兰州大学第一医院呼吸与危重症医学科,兰州  730000,甘肃

  • 收稿日期:2023-09-20 修回日期:2023-11-27 出版日期:2024-05-26 发布日期:2024-04-16
  • 通讯作者: 李龙,男,硕士,主任医师,硕士研究生导师,研究方向:肺间质纤维化。 E-mail: llqqdbd@163.com
  • 作者简介:陈凤,女,硕士研究生,研究方向:肺间质纤维化。 E-mail: 3363901682@qq.com
  • 基金资助:
    甘肃省科技计划项目(20JR10RA697)

Research progress on CXC chemokines and their receptors and pulmonary fibrosis

CHEN Feng1, LI Long2, WANG Jie1, LIU Shengfei 1   

  1. 1First Clinical School of Lanzhou University, Lanzhou 730000, Gansu, China; 2Department of Respiratory and Critical Care Medicine, First Hospital of Lanzhou University, Lanzhou 730000, Gansu, China
  • Received:2023-09-20 Revised:2023-11-27 Online:2024-05-26 Published:2024-04-16

摘要:

肺纤维化(pulmonary fibrosis,PF)是一种常见的、持续发展的、无法逆转的、致命的慢性肺部疾病,诊断后的中位生存期为2~4年,其特征是肺部细胞外基质沉积过多和瘢痕,导致功能衰竭、严重呼吸问题甚至死亡。大量研究表明,CXC趋化因子及其受体在肺纤维化和其他纤维增生紊乱的疾病中发挥重要作用。多项研究显示,CXC趋化因子可能成为许多疾病治疗的新靶点。本文主要对关键CXC趋化因子及其受体在肺纤维化中的作用作一综述,以期为肺纤维化的治疗提供参考。

关键词: 肺纤维化, CXC趋化因子, CXC趋化因子受体

Abstract:

Pulmonary fibrosis (PF) is a common, persistent, irreversible, fatal chronic lung disease with a median survival of 2-4 years after diagnosis. It is characterized by excessive extracellular matrix deposition and scarring in the lungs, leading to functional failure, severe respiratory problems and even death. Numerous studies have shown that CXC chemokines and their receptors play important roles in PF and other desmoplastic disorders. Several studies have shown that chemokines may become new targets for the treatment of many diseases. Here, we review the role of key CXC chemokines and their receptors in PF to provide a reference for the treatment of PF.

Key words: pulmonary fibrosis, CXC chemokine, CXC chemokine receptor

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