Rand Jacob H, Taatjes Douglas J
Department of Pathology and Laboratory Medicine, Weill Cornell Medical College, New York, NY, USA.
Department of Pathology and Laboratory Medicine, and Microscopy Imaging Center, Larner College of Medicine, University of Vermont, 89 Beaumont Avenue, Burlington, VT, 05405, USA.
Histochem Cell Biol. 2018 Nov;150(5):529-543. doi: 10.1007/s00418-018-1709-2. Epub 2018 Aug 18.
The antiphospholipid syndrome (APS) is an autoimmune thrombophilic disorder that was described as a diagnostic entity over 30 years ago. And yet the pathogenic mechanisms that are responsible for its clinical manifestations remain to be definitively established. The syndrome is defined by (1) the concurrence of vascular thrombosis and/or pregnancy complications together with (2) positivity for immunoassays and coagulation tests that were derived from clinical observations of two anomalous laboratory test results-specifically, false positivity for syphilis infection in uninfected individuals and the finding of inhibitors of blood coagulation in patients who lacked any bleeding tendencies. Over the years, these were standardized into immunoassays and coagulation assays for APS. Here, we describe how prior knowledge of the immunologic and coagulation aspects of the disorder led to research involving a range of imaging modalities including light microscopy, immunohistochemistry, confocal scanning laser microscopy, transmission and scanning electron microscopy, and atomic force microscopy. In turn, the results from those studies led to a "reimagining" of APS that has advanced the understanding of pathogenic mechanisms of the disorder and has led to the development of novel mechanistically based diagnostics along with potential new treatment approaches that target disease mechanisms.
抗磷脂综合征(APS)是一种自身免疫性血栓形成倾向疾病,早在30多年前就被描述为一种诊断实体。然而,导致其临床表现的致病机制仍有待明确确立。该综合征的定义为:(1)血管血栓形成和/或妊娠并发症同时存在,以及(2)免疫测定和凝血试验呈阳性,这是基于对两种异常实验室检查结果的临床观察得出的——具体而言,未感染个体梅毒感染检测呈假阳性,以及在无任何出血倾向的患者中发现凝血抑制剂。多年来,这些检测已被标准化为APS的免疫测定和凝血测定。在此,我们描述了对该疾病免疫和凝血方面的先验知识如何推动了一系列成像方式的研究,包括光学显微镜、免疫组织化学、共聚焦扫描激光显微镜、透射和扫描电子显微镜以及原子力显微镜。反过来,这些研究结果促使人们对APS进行“重新认识”,加深了对该疾病致病机制的理解,并推动了基于机制的新型诊断方法的开发以及针对疾病机制的潜在新治疗方法的发展。