Université de Strasbourg, INSERM, Etablissement Français du Sang (EFS) Grand Est, BPPS UMR_S1255, Fédération de Médecine Translationnelle de Strasbourg (FMTS), Strasbourg, France.
Hôpitaux Universitaires de Strasbourg, Anesthésie, Réanimation et Médecine périopératoire, Nouvel Hôpital Civil, Strasbourg, France.
J Thromb Haemost. 2022 Feb;20(2):449-460. doi: 10.1111/jth.15583. Epub 2021 Nov 17.
The specific role of platelets during sepsis is not yet fully understood, probably related to the paradox of platelets being potentially beneficial but also deleterious via their thrombotic functions.
To evaluate the impact of thrombocytopenia on septic shock in mice and to investigate whether transfusion of fresh washed platelets, either fully functional or with impaired hemostatic properties, might have beneficial effects.
Septic shock was induced by cecal ligation and puncture (CLP). Experimental depletion of circulating platelets was induced with a rat anti-mouse GPIbα monoclonal antibody. Transfusion of either wild-type washed platelets, platelets treated with the antiplatelet drugs acetylsalicylic acid (ASA) and clopidogrel, or GPIIbIIIa-deficient washed platelets treated with ASA and clopidogrel was performed 4 h after CLP surgery.
Depletion of circulating platelets negatively affected septic shock, worsening systemic inflammation, coagulopathy, organ damage, and mortality, raising the question of whether a higher platelet count could be protective. Transfusion of fully functional platelets or platelets with combined treatment with ASA and clopidogrel, with or without additional GPIIbIIIa deficiency, afforded an immediate return of circulating platelet counts to their initial values before surgery. However, transfusion of each of the three types of platelets did not prevent arterial hypotension, inflammatory response, coagulopathy, and organ damage during septic shock.
Depletion of circulating platelets negatively affects septic shock, while transfusion of washed platelets has no significant beneficial effect in mice.
血小板在脓毒症中的具体作用尚不完全清楚,这可能与血小板通过其血栓形成功能具有潜在益处但也具有有害作用的矛盾有关。
评估血小板减少症对脓毒性休克小鼠的影响,并研究输注新鲜洗涤血小板(功能正常或止血功能受损)是否可能具有有益作用。
通过盲肠结扎和穿刺(CLP)诱导脓毒性休克。用抗鼠 GPIbα 单克隆抗体诱导循环血小板的实验性耗竭。在 CLP 手术后 4 小时输注野生型洗涤血小板、用抗血小板药物乙酰水杨酸(ASA)和氯吡格雷处理的血小板或用 ASA 和氯吡格雷处理的缺乏 GPIIbIIIa 的洗涤血小板。
循环血小板耗竭对脓毒性休克产生负面影响,加重全身炎症、凝血障碍、器官损伤和死亡率,这引发了一个问题,即更高的血小板计数是否具有保护作用。输注功能正常的血小板或用 ASA 和氯吡格雷联合治疗的血小板,无论是否伴有额外的 GPIIbIIIa 缺乏,均可使循环血小板计数立即恢复到手术前的初始值。然而,输注这三种类型的血小板中的任何一种都不能防止脓毒性休克期间的动脉低血压、炎症反应、凝血障碍和器官损伤。
循环血小板耗竭对脓毒性休克产生负面影响,而输注洗涤血小板对小鼠没有显著的有益作用。