Sinha Urshita, Setty Suman, Pilon Céleste, Brown Julia J, Ruiz Maria Armila, Ren Guohui, Rauch Joyce, Saraf Santosh L, Levine Jerrold S
Division of Nephrology, Department of Medicine, University of Illinois at Chicago, Chicago, Illinois, USA.
Department of Pathology, University of Illinois at Chicago, Chicago, Illinois, USA.
Br J Haematol. 2025 Apr;206(4):1213-1217. doi: 10.1111/bjh.19972. Epub 2025 Jan 2.
We describe a patient with sickle cell disease (SCD) and elevated antiphospholipid antibodies (aPL) who developed multi-organ failure resembling catastrophic antiphospholipid syndrome. Autoimmune screening revealed several autoantibodies characteristic of systemic lupus erythematosus (SLE). Notably, routinely housed and unmanipulated transgenic sickle mice displayed significantly elevated titres of aPL- and SLE-associated autoantibodies. We hypothesize that SCD may be a risk factor not only for the development of aPL but also more widespread autoimmunity.
我们描述了一名患有镰状细胞病(SCD)且抗磷脂抗体(aPL)升高的患者,该患者出现了类似于灾难性抗磷脂综合征的多器官功能衰竭。自身免疫筛查发现了几种系统性红斑狼疮(SLE)特有的自身抗体。值得注意的是,常规饲养且未进行操作的转基因镰状小鼠显示出aPL和SLE相关自身抗体的滴度显著升高。我们推测,SCD可能不仅是aPL产生的危险因素,也是更广泛自身免疫的危险因素。