Center for Pulmonary and Vascular Biology, Department of Pediatrics, UT Southwestern Medical Center, Dallas, TX, United States.
Center for Pulmonary and Vascular Biology, Department of Pediatrics, UT Southwestern Medical Center, Dallas, TX, United States.
Clin Immunol. 2023 Oct;255:109745. doi: 10.1016/j.clim.2023.109745. Epub 2023 Aug 23.
The antiphospholipid syndrome (APS) is an autoimmune disease characterized by the persistent presence of antibodies directed against phospholipids and phospholipid-binding proteins that are associated with thrombosis and pregnancy-related morbidity. The latter includes fetal deaths, premature birth and maternal complications. In the early 1990s, a distinct set of autoantibodies, termed collectively antiphospholipid antibodies (aPL), were identified as the causative agents of this disorder. Subsequently histological analyses of the placenta from APS pregnancies revealed various abnormalities, including inflammation at maternal-fetal interface and poor placentation manifested by reduced trophoblast invasion and limited uterine spiral artery remodeling. Further preclinical investigations identified the molecular targets of aPL and the downstream intracellular pathways of key placental cell types. While these discoveries suggest potential therapeutics for this disorder, definitive clinical trials have not been completed. This concise review focuses on the recent developments in the field of basic and translational research pursuing novel mechanisms underlying obstetric APS.
抗磷脂综合征(APS)是一种自身免疫性疾病,其特征为持续存在针对与血栓形成和妊娠相关发病率相关的磷脂和磷脂结合蛋白的抗体。后者包括胎儿死亡、早产和产妇并发症。在 20 世纪 90 年代初,一组称为抗磷脂抗体(aPL)的独特自身抗体被确定为这种疾病的致病因素。随后,对 APS 妊娠胎盘的组织学分析显示出各种异常,包括母体-胎儿界面的炎症和胎盘形成不良,表现为滋养细胞侵袭减少和子宫螺旋动脉重塑有限。进一步的临床前研究确定了 aPL 的分子靶点和关键胎盘细胞类型的细胞内下游途径。虽然这些发现为这种疾病提供了潜在的治疗方法,但尚未完成明确的临床试验。本综述重点介绍了基础和转化研究领域在探索产科 APS 潜在机制方面的最新进展。