Service de Rhumatologie, Centre de référence des maladies auto-immunes systémiques rares RESO, Hôpitaux Universitaires de Strasbourg, Strasbourg, France.
Department of Medicine, Beth Israel Deaconess Medical Center, Boston, MA, USA.
Nat Rev Immunol. 2023 Aug;23(8):495-510. doi: 10.1038/s41577-023-00834-4. Epub 2023 Jan 27.
Immune-mediated inflammatory diseases (IMIDs) are characterized by excessive and uncontrolled inflammation and thrombosis, both of which are responsible for organ damage, morbidity and death. Platelets have long been known for their role in primary haemostasis, but they are now also considered to be components of the immune system and to have a central role in the pathogenesis of IMIDs. In patients with IMIDs, platelets are activated by disease-specific factors, and their activation often reflects disease activity. Here we summarize the evidence showing that activated platelets have an active role in the pathogenesis and the progression of IMIDs. Activated platelets produce soluble factors and directly interact with immune cells, thereby promoting an inflammatory phenotype. Furthermore, platelets participate in tissue injury and promote abnormal tissue healing, leading to fibrosis. Targeting platelet activation and targeting the interaction of platelets with the immune system are novel and promising therapeutic strategies in IMIDs.
免疫介导的炎症性疾病(IMIDs)的特征是过度和失控的炎症和血栓形成,这两者都可导致器官损伤、发病率和死亡率。血小板长期以来一直被认为在初级止血中起作用,但现在也被认为是免疫系统的组成部分,并在 IMIDs 的发病机制中起核心作用。在 IMIDs 患者中,血小板被疾病特异性因子激活,其激活通常反映疾病活动度。在这里,我们总结了表明激活的血小板在 IMIDs 的发病机制和进展中具有积极作用的证据。激活的血小板产生可溶性因子,并直接与免疫细胞相互作用,从而促进炎症表型。此外,血小板参与组织损伤并促进异常组织愈合,导致纤维化。针对血小板激活和血小板与免疫系统相互作用的靶向治疗是 IMIDs 中新颖且有前途的治疗策略。
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