Systemic lupus erythematosus-associated autoantibodies in sickle cell disease: Spontaneous emergence in a patient and in transgenic sickle mice.

IF 5.1 2区 医学 Q1 HEMATOLOGY
Urshita Sinha, Suman Setty, Céleste Pilon, Julia J Brown, Maria Armila Ruiz, Guohui Ren, Joyce Rauch, Santosh L Saraf, Jerrold S Levine
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引用次数: 0

Abstract

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.

镰状细胞病中的系统性红斑狼疮相关自身抗体:在患者和转基因镰状细胞小鼠中自发出现。
我们描述了一位镰状细胞病(SCD)和抗磷脂抗体(aPL)升高的患者,他们发展成类似灾难性抗磷脂综合征的多器官衰竭。自身免疫筛查显示了系统性红斑狼疮(SLE)的几种自身抗体特征。值得注意的是,常规饲养和未处理的转基因镰状小鼠显示出显著升高的aPL-和sle相关自身抗体滴度。我们假设SCD可能不仅是aPL发展的危险因素,而且是更广泛的自身免疫的危险因素。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
8.60
自引率
4.60%
发文量
565
审稿时长
1 months
期刊介绍: The British Journal of Haematology publishes original research papers in clinical, laboratory and experimental haematology. The Journal also features annotations, reviews, short reports, images in haematology and Letters to the Editor.
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