HMGB1在急性肺损伤/急性呼吸窘迫综合征中的研究进展
DOI:
CSTR:
作者:
作者单位:

作者简介:

通讯作者:

中图分类号:

基金项目:


Research progress of high mobility group box-1 in acute lung injury/acute respiratory distress syndrome
Author:
Affiliation:

Fund Project:

  • 摘要
  • |
  • 图/表
  • |
  • 访问统计
  • |
  • 参考文献
  • |
  • 相似文献
  • |
  • 引证文献
  • |
  • 资源附件
  • |
  • 文章评论
    摘要:

    急性肺损伤(acute lung ingury,ALI)和急性呼吸窘迫综合征(acute respiratory distress syndrome,ARDS)是ICU内危及患者生命的临床综合征。目前ARDS的病死率仍居高不下(>40%) [1]。其治疗和早期运用生物学标记诊断仍是重症医学领域的重大难题。高迁移率族蛋白B1(high mobility group box-1 protein,HMGB1)是一种新近发现的重要的晚期炎性介质,与脓毒症、恶性肿瘤、免疫性疾病等许多疾病相关。HMGB1作为一种警报素,其浓度的高低可以反映机体炎症及组织损伤的严重程度,并与疾病的预后密切相关。HMGB1可能会为阻断炎症通路的级联反应提供新的治疗靶点。本文就HMGB1在ALI/ARDS中的研究进展做一综述。

    Abstract:

    Acute lung injury(ALI) and acute respiratory distress syndrome(ARDS) are life-threatening clinical syndromes in the in-tensive care unit. At present,ARDS mortality rate remains high(>40%). Its treatment and the use of biological markers for early di-agnosis are still major problems in the field of critical care medicine. High mobility group box-1 protein(HMGB1) has recently been identified as a new proinflammatory cytokine and late mediator of inflammation. It is associated with sepsis,cancer,autoimmune dis-eases and many other diseases. HMGB1 is an alarmin its concentration can reflect the severity of the inflammatory and tissue injury,and is closely related with the prognosis of the disease. Antagonizing HMGB1 can block the cascade of inflammatory pathways,which may provide a new therapeutic target for the treatment of ARDS.In this paper,we reviewed on the role of HMGB1 in ALI/ARDS.

    参考文献
    相似文献
    引证文献
引用本文

高 峰,徐 昉. HMGB1在急性肺损伤/急性呼吸窘迫综合征中的研究进展[J].重庆医科大学学报,2014,38(9):1193-1196

复制
分享
相关视频

文章指标
  • 点击次数:
  • 下载次数:
  • HTML阅读次数:
  • 引用次数:
历史
  • 收稿日期:
  • 最后修改日期:
  • 录用日期:
  • 在线发布日期: 2014-12-03
  • 出版日期:
文章二维码