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血小板-嗜酸性粒细胞相互作用作为变应性炎症和哮喘的潜在治疗靶点

Platelet-Eosinophil Interactions As a Potential Therapeutic Target in Allergic Inflammation and Asthma.

作者信息

Shah Sajeel A, Page Clive P, Pitchford Simon C

机构信息

Sackler Institute of Pulmonary Pharmacology, Institute of Pharmaceutical Science, King's College London, London, United Kingdom.

出版信息

Front Med (Lausanne). 2017 Aug 8;4:129. doi: 10.3389/fmed.2017.00129. eCollection 2017.

Abstract

The importance of platelet activation during hemostasis is well understood. An understanding of these mechanisms has led to the use of several classes of anti-platelet drugs to inhibit aggregation for the prevention of thrombi during cardiovascular disease. It is now also recognized that platelets can function very differently during inflammation, as part of their role in the innate immune response against pathogens. This dichotomy in platelet function occurs through distinct physiological processes and alternative signaling pathways compared to that of hemostasis (leading to platelet aggregation) and is manifested as increased rheological interactions with leukocytes, the ability to undergo chemotaxis, communication with antigen-presenting cells, and direct anti-pathogen responses. Mounting evidence suggests platelets are also critical in the pathogenesis of allergic diseases such as asthma, where they have been associated with antigen presentation, bronchoconstriction, bronchial hyperresponsiveness, airway inflammation, and airway remodeling in both clinical and experimental studies. In particular, platelets have been reported bound to eosinophils in the blood of patients with asthma and the incidence of these events increases after both spontaneous asthma attacks in a biphasic manner, or after allergen challenge in the clinic. Platelet depletion in animal models of allergic airway inflammation causes a profound reduction in eosinophil recruitment to the lung, suggesting that the association of platelets with eosinophils is indeed an important event during eosinophil activation. Furthermore, in cases of severe asthma, and in animal models of allergic airways inflammation, platelet-eosinophil complexes move into the lung through a platelet P-selectin-mediated, eosinophil β1-integrin activation-dependent process, while platelets increase adherence of eosinophils to the vascular endothelium , demonstrating a clear interaction between these cell types in allergic inflammatory diseases. This review will explore non-thrombotic platelet activation in the context of allergy and the association of platelets with eosinophils, to reveal how these phenomena may lead to the discovery of novel therapeutic targets.

摘要

血小板激活在止血过程中的重要性已得到充分理解。对这些机制的认识促使人们使用几类抗血小板药物来抑制聚集,以预防心血管疾病期间的血栓形成。现在人们也认识到,血小板在炎症过程中的功能可能非常不同,这是它们在针对病原体的固有免疫反应中所起作用的一部分。与止血过程(导致血小板聚集)相比,血小板功能的这种二分法通过不同的生理过程和替代信号通路发生,表现为与白细胞的流变学相互作用增加、趋化能力、与抗原呈递细胞的通讯以及直接的抗病原体反应。越来越多的证据表明,血小板在哮喘等过敏性疾病的发病机制中也至关重要,在临床和实验研究中,它们与抗原呈递、支气管收缩、支气管高反应性、气道炎症和气道重塑有关。特别是,据报道,哮喘患者血液中的血小板与嗜酸性粒细胞结合,并且在自发性哮喘发作以双相方式发作后或在临床进行过敏原激发后,这些事件的发生率都会增加。过敏性气道炎症动物模型中的血小板耗竭会导致肺中嗜酸性粒细胞募集的显著减少,这表明血小板与嗜酸性粒细胞的结合确实是嗜酸性粒细胞激活过程中的一个重要事件。此外,在严重哮喘病例以及过敏性气道炎症动物模型中,血小板 - 嗜酸性粒细胞复合物通过血小板P选择素介导的、嗜酸性粒细胞β1整合素激活依赖性过程进入肺部,而血小板会增加嗜酸性粒细胞与血管内皮的粘附,这表明这些细胞类型在过敏性炎症疾病中存在明显的相互作用。本综述将探讨过敏背景下的非血栓性血小板激活以及血小板与嗜酸性粒细胞的关联,以揭示这些现象如何可能导致发现新的治疗靶点。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/efe6/5550710/0659cb91932c/fmed-04-00129-g001.jpg

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