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转化生长因子-β:急性呼吸窘迫综合征中细胞调节的介质

Transforming growth factor-beta: a mediator of cell regulation in acute respiratory distress syndrome.

作者信息

Dhainaut Jean-François, Charpentier Julien, Chiche Jean-Daniel

机构信息

Service de Réanimation Médicale, Pavillon Cornil, Faculté Cochin Port-Royal, Université Paris 5, Hôpital Cochin, Paris Cedex 14, France.

出版信息

Crit Care Med. 2003 Apr;31(4 Suppl):S258-64. doi: 10.1097/01.CCM.0000057901.92381.75.

Abstract

OBJECTIVE

To review recent advances in the use of transforming growth factor (TGF)-beta in acute lung injury and to apply this knowledge to understanding the pathophysiology of this syndrome.

DATA SOURCES AND STUDY SELECTION

Published research and review articles in the English language related to the role of TGF-beta in acute lung injury.

DATA EXTRACTION AND SYNTHESIS

The cytokine TGF-beta plays a critical role in the resolution of tissue injury in multiple organs, including the lung. Following injury, TGF-beta has been most thoroughly evaluated during the late phases of tissue repair, where it plays a critical role in the development of pulmonary fibrosis. In contrast, recent animal studies showed that expression levels of several TGF-beta-inducible genes were dramatically increased as early as 2 days after the induction of injury. The integrin alpha(v)beta(6) activates latent TGF-beta in the lungs. Mice lacking this integrin were completely protected from pulmonary edema in a model of bleomycin-induced acute lung injury. Pharmacologic inhibition of TGF-beta also protected wild-type mice from pulmonary edema induced by bleomycin or Escherichia coli endotoxin. Similar findings also have been reported in patients in a clinical study evaluating TGF-beta in the bronchoalveolar lavage fluid during the course of acute respiratory distress syndrome (ARDS). Indeed, the bronchoalveolar lavage concentrations were dramatically increased as early as 1 day after the initiation of ARDS criteria and were correlated with decreases in the Pao(2)/Fio(2) ratio, suggesting an important role for TGF-b1 in the development of ARDS in humans.

CONCLUSIONS

These studies suggest that TGF-beta not only participates in the late phase of acute lung injury, but also might be active early in acute lung injury and potentially could contribute to the development of pulmonary edema. Integrin-mediated local activation of TGF-beta is critical to the development of pulmonary edema in ARDS, and blocking TGF-beta or its activation could be an effective treatment for this disorder.

摘要

目的

回顾转化生长因子(TGF)-β在急性肺损伤中的应用进展,并运用这些知识理解该综合征的病理生理学。

资料来源与研究选择

以英文发表的与TGF-β在急性肺损伤中的作用相关的研究及综述文章。

资料提取与综合

细胞因子TGF-β在包括肺在内的多个器官的组织损伤修复中起关键作用。损伤后,TGF-β在组织修复后期得到了最充分的评估,它在肺纤维化的发展中起关键作用。相比之下,最近的动物研究表明,早在损伤诱导后2天,几种TGF-β诱导基因的表达水平就显著增加。整合素α(v)β(6)可激活肺中的潜伏TGF-β。在博来霉素诱导的急性肺损伤模型中,缺乏这种整合素的小鼠完全免受肺水肿的影响。对TGF-β的药理抑制也可保护野生型小鼠免受博来霉素或大肠杆菌内毒素诱导的肺水肿。在一项评估急性呼吸窘迫综合征(ARDS)病程中支气管肺泡灌洗液中TGF-β的临床研究中,患者也有类似发现。事实上,早在ARDS标准启动后1天,支气管肺泡灌洗浓度就显著增加,并与动脉血氧分压(Pao₂)/吸入氧分数值(Fio₂)比值降低相关,提示TGF-β1在人类ARDS的发展中起重要作用。

结论

这些研究表明,TGF-β不仅参与急性肺损伤的后期阶段,还可能在急性肺损伤早期就发挥作用,并可能导致肺水肿的发生。整合素介导的TGF-β局部激活对ARDS中肺水肿的发展至关重要,阻断TGF-β或其激活可能是治疗该疾病的有效方法。

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