Staphylococcus aureus bacteremia (SAB) remains a clinically challenging infection despite extensive investigation. Repurposing medications approved for other indications is appealing as clinical safety profiles have already been established. Ticagrelor, a reversible adenosine diphosphate receptor antagonist that prevents platelet aggregation, is indicated for patients suffering from acute coronary syndrome (ACS). However, some clinical data suggest that patients treated with ticagrelor are less likely to have poor outcomes due to S. aureus infection. There are several potential mechanisms by which ticagrelor may affect S. aureus virulence. These include direct antibacterial activity, up-regulation of the innate immune system through boosting platelet-mediated S. aureus killing, and prevention of S. aureus adhesion to host tissues. In this Pearl, we review the clinical data surrounding ticagrelor and infection as well as explore the evidence surrounding these proposed mechanisms of action. While more evidence is needed before antiplatelet medications formally become part of the arsenal against S. aureus infection, these potential mechanisms represent exciting pathways to target in the host/pathogen interface.
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机译:尽管进行了广泛的调查,但金黄色葡萄球菌菌血症 (SAB) 仍然是一种临床上具有挑战性的感染。重新利用批准用于其他适应症的药物很有吸引力,因为临床安全性概况已经确定。替格列罗是一种可逆的二磷酸腺苷受体拮抗剂,可防止血小板聚集,适用于急性冠状动脉综合征 (ACS) 患者。然而,一些临床数据表明,接受替格瑞洛治疗的患者不太可能因金黄色葡萄球菌感染而出现不良结局。替格瑞洛可能影响金黄色葡萄球菌毒力的几种潜在机制。这些包括直接抗菌活性、通过促进血小板介导的金黄色葡萄球菌杀伤上调先天免疫系统以及防止金黄色葡萄球菌粘附到宿主组织。在本期 Pearl 中,我们回顾了围绕替格瑞洛和感染的临床数据,并探讨了围绕这些拟议的作用机制的证据。虽然在抗血小板药物正式成为对抗金黄色葡萄球菌感染的武器库的一部分之前需要更多的证据,但这些潜在机制代表了在宿主/病原体界面中靶向的令人兴奋的途径。
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