在已有自身免疫的患者中,辉瑞生物技术公司的COVID-19 RNA疫苗可诱导磷脂酰丝氨酸自身抗体、冷球蛋白血症和数字坏死

Sandy Nasr, Sara Khalil, Bernard J. Poiesz, Katalin Banki, Andras Perl
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引用次数: 6

摘要

我们描述了一名64岁的白人女性,她有雷诺病、手部关节炎、光敏性、干燥综合征和白细胞分裂性血管炎的病史,在接受第一剂辉瑞- biontech COVID-19 RNA疫苗后三天开始出现逐渐恶化的指尖坏死。我们的检查结果显示冷球蛋白血症、低补体血症、抗核抗体(ANA)和针对磷脂酰丝氨酸(aPL- ps)的IgM抗磷脂自身抗体(aPL)升高,提示诊断为系统性红斑狼疮(SLE)和抗磷脂综合征(APS)。该患者在接种疫苗两个月后仍未产生抗刺突IgG抗体。通过血浆置换、抗凝和免疫抑制,疾病进展得以停止。我们得出结论,疫苗RNA片段可能诱发SLE,表现为APS、冷球蛋白血症、低补体血症和指状坏死。
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Pfizer–biontech COVID-19 RNA vaccination induces phosphatidylserine autoantibodies, cryoglobulinemia, and digital necrosis in a patient with pre-existing autoimmunity

We describe a 64-year-old Caucasian female with a history of Raynaud's disease, hand arthritis, photosensitivity, Sjogren's syndrome and leukocytoclastic vasculitis who presented with progressively worsening fingertip necrosis that began three days after receiving a first dose of Pfizer–BioNTech COVID-19 RNA vaccine. Our workup revealed cryoglobulinemia, hypocomplementemia, elevated antinuclear antibodies (ANA) and IgM antiphospholipid autoantibodies (aPL) directed against phosphatidylserine (aPL-PS), suggesting a diagnosis of systemic lupus erythematosus (SLE) and antiphospholipid syndrome (APS). The patient failed to develop anti-spike IgG antibodies up to two months following vaccination. Disease progression was halted by plasmapheresis, anticoagulation, and immune suppression. We conclude that the vaccine RNA moiety may induce SLE manifesting in APS, cryoglobulinemia, hypocomplementemia, and digital necrosis.

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