Laboratory of Thrombosis and Hemostasis and Valvular Heart Disease, GIGA-Cardiovascular Sciences, Department of Cardiology, University of Liège, CHU Sart-Tilman, Liège, Belgium.
Department of Laboratory Hematology, CHU Sart-Tilman, Liège, Belgium.
J Thromb Haemost. 2017 May;15(5):983-997. doi: 10.1111/jth.13669. Epub 2017 Apr 13.
Essentials CpG oligodeoxynucleotide (ODN) immuotherapeutics cause undesired platelet activating effects. It is crucial to understand the mechanisms of these effects to identify protective strategies. CpG ODN-induced platelet activation depends on C-type lectin-like receptor 2 (CLEC-2) and P2Y12. Targeting CLEC-2 or P2Y12 fully prevents CpG ODN-induced platelet activation and thrombosis.
Background Synthetic phosphorothioate-modified CpG oligodeoxynucleotides (ODNs) show potent immunostimulatory properties that are widely exploited in clinical trials of anticancer treatment. Unexpectedly, a recent study indicated that CpG ODNs activate human platelets via the immunoreceptor tyrosine-based activation motif (ITAM)-coupled receptor glycoprotein VI. Objective To further analyze the mechanisms of CpG ODN-induced platelet activation and identify potential inhibitory strategies. Methods In vitro analyses were performed on human and mouse platelets, and on cell lines expressing platelet ITAM receptors. CpG ODN platelet-activating effects were evaluated in a mouse model of thrombosis. Results We demonstrated platelet uptake of CpG ODNs, resulting in platelet activation and aggregation. C-type lectin-like receptor 2 (CLEC-2) expressed in DT40 cells bound CpG ODNs. CpG ODN uptake did not occur in CLEC-2-deficient mouse platelets. Inhibition of human CLEC-2 with a blocking antibody inhibited CpG ODN-induced platelet aggregation. CpG ODNs caused CLEC-2 dimerization, and provoked its internalization. They induced dense granule release before the onset of aggregation. Accordingly, pretreating platelets with apyrase, or inhibiting P2Y12 with cangrelor or clopidogrel, prevented CpG ODN platelet-activating effect. In vivo, intravenously injected CpG ODN interacted with platelets adhered to mouse injured endothelium, and promoted thrombus growth, which was inhibited by CLEC-2 deficiency or by clopidogrel. Conclusions CLEC-2 and P2Y12 are required for CpG ODN-induced platelet activation and thrombosis, and might be targeted to prevent adverse events in patients at risk.
Essentials CpG 寡脱氧核苷酸(ODN)免疫疗法会引起血小板的非预期激活作用。了解这些作用的机制对于确定保护策略至关重要。CpG ODN 诱导的血小板激活依赖于 C 型凝集素样受体 2(CLEC-2)和 P2Y12。靶向 CLEC-2 或 P2Y12 可完全阻止 CpG ODN 诱导的血小板激活和血栓形成。
背景:合成的硫代磷酸修饰的 CpG 寡核苷酸(ODN)具有强大的免疫刺激特性,在癌症治疗的临床试验中得到了广泛的应用。出乎意料的是,最近的一项研究表明,CpG ODN 通过免疫受体酪氨酸基激活基序(ITAM)偶联受体糖蛋白 VI 激活人血小板。目的:进一步分析 CpG ODN 诱导血小板激活的机制,并确定潜在的抑制策略。方法:在人源和鼠源血小板、表达血小板 ITAM 受体的细胞系中进行体外分析。在血栓形成的小鼠模型中评估 CpG ODN 对血小板的激活作用。结果:我们发现 CpG ODN 可被血小板摄取,导致血小板激活和聚集。在 DT40 细胞中表达的 C 型凝集素样受体 2(CLEC-2)与 CpG ODN 结合。CLEC-2 缺陷型鼠源血小板中不存在 CpG ODN 的摄取。用阻断抗体抑制人 CLEC-2 可抑制 CpG ODN 诱导的血小板聚集。CpG ODN 诱导 CLEC-2 二聚化,并引发其内化。它们在聚集开始之前引起致密颗粒的释放。因此,用 apyrase 预处理血小板,或用坎格雷洛或氯吡格雷抑制 P2Y12,可防止 CpG ODN 对血小板的激活作用。在体内,静脉注射的 CpG ODN 与黏附在小鼠受伤内皮细胞上的血小板相互作用,并促进血栓形成,CLEC-2 缺陷或氯吡格雷可抑制这一作用。结论:CLEC-2 和 P2Y12 是 CpG ODN 诱导的血小板激活和血栓形成所必需的,可能成为预防高危患者不良事件的靶点。