CXCR2/CXCR2配体在急性肺损伤中的作用

Robert M Strieter, Michael P Keane, Marie D Burdick, Ammar Sakkour, Lynne A Murray, John A Belperio
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引用次数: 37

摘要

尽管我们的知识和重症监护有所进步,急性肺损伤(ALI)和急性呼吸窘迫综合征(ARDS)的死亡率仍然很高。这支持了我们需要进一步了解参与ARDS发病机制的介质的观点。ARDS的发病机制是一个连续的过程,从渗出和炎症到弥漫性肺泡损伤的纤维增殖阶段。虽然许多介质参与ARDS的发病机制,但CXC趋化因子家族的成员已被确定在促进炎症细胞的募集以及在ARDS的两个阶段介导异常血管重构中发挥关键和多效性作用。本文将讨论CXC趋化因子在ALI/ARDS中的生物学意义。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
The role of CXCR2/CXCR2 ligands in acute lung injury.

The mortality of acute lung injury (ALI) and acute respiratory distress syndrome (ARDS) remain high despite advances in our knowledge and intensive care. This supports the contention that we need to further our understanding of the mediators that are involved in the pathogenesis of ARDS. The pathogenesis of ARDS proceeds as a continuum from exudation and inflammation to a fibroproliferative phase of diffuse alveolar damage. While a number of mediators are involved in the pathogenesis of ARDS, members of the CXC chemokine family have been determined to play a critical and pleiotropic role in promoting both recruitment of inflammatory cells, as well as in mediating aberrant vascular remodeling during both phases of ARDS. The importance of the biology of CXC chemokines in ALI/ARDS will be discussed in this review.

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