Microvesicles as new therapeutic targets for the treatment of the acute respiratory distress syndrome (ARDS)

被引:5
|
作者
Soni, Sanooj [1 ]
Tirlapur, Nikhil [1 ]
O'Dea, Kieran P. [1 ]
Takata, Masao [1 ]
Wilson, Michael R. [1 ]
机构
[1] Imperial Coll London, Chelsea & Westminster Hosp, Fac Med, Sect Anaesthet Pain Med & Intens Care, 369 Fulham Rd, London SW10 9NH, England
基金
英国生物技术与生命科学研究理事会; 英国医学研究理事会;
关键词
Acute lung injury; acute respiratory distress syndrome; cellular communication; extracellular vesicles; microvesicles; ACUTE LUNG INJURY; EXTRACELLULAR VESICLES; MECHANICAL VENTILATION; PLATELET MICROPARTICLES; INFLAMMATORY RESPONSES; MACROPHAGES; CELLS; OUTCOMES; RELEASE; DYSFUNCTION;
D O I
10.1080/14728222.2019.1692816
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Introduction: Acute respiratory distress syndrome (ARDS) is a heterogeneous and multifactorial disease; it is a common and devastating condition that has a high mortality. Treatment is limited to supportive measures hence novel pharmacological approaches are necessary. We propose a new direction in ARDS research; this means moving away from thinking about individual inflammatory mediators and instead investigating how packaged information is transmitted between cells. Microvesicles (MVs) represent a novel vehicle for inter-cellular communication with an emerging role in ARDS pathophysiology. Areas covered: This review examines current approaches to ARDS and emerging MV research. We describe advances in our understanding of microvesicles and focus on their pro-inflammatory roles in airway and endothelial signaling. We also offer reasons for why MVs are attractive therapeutic targets. Expert opinion: MVs have a key role in ARDS pathophysiology. Preclinical studies must move away from simple models toward more realistic scenarios while clinical studies must embrace patient heterogeneity. Microvesicles have the potential to aid identification of patients who may benefit from particular treatments and act as biomarkers of cellular status and disease progression. Understanding microvesicle cargoes and their cellular interactions will undoubtedly uncover new targets for ARDS.
引用
收藏
页码:931 / 941
页数:11
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