Pfizer-biontech COVID-19 RNA vaccination induces phosphatidylserine autoantibodies, cryoglobulinemia, and digital necrosis in a patient with pre-existing autoimmunity.

Clinical Immunology Communications Pub Date : 2021-12-01 Epub Date: 2021-09-27 DOI:10.1016/j.clicom.2021.08.001
Sandy Nasr, Sara Khalil, Bernard J Poiesz, Katalin Banki, Andras Perl
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Abstract

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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辉瑞-生物技术公司的 COVID-19 RNA 疫苗接种会诱发一名已存在自身免疫的患者出现磷脂酰丝氨酸自身抗体、低温球蛋白血症和数字坏死。
我们描述了一名 64 岁的白种女性,她有雷诺氏病、手关节炎、光敏感性、Sjogren 综合征和白细胞凝集性血管炎病史,在接种第一剂辉瑞-生物技术公司 COVID-19 RNA 疫苗三天后开始出现逐渐加重的指尖坏死。我们的检查发现了低温球蛋白血症、低补体血症、抗核抗体(ANA)升高和针对磷脂酰丝氨酸的 IgM 抗磷脂自身抗体(aPL)(aPL-PS),提示诊断为系统性红斑狼疮(SLE)和抗磷脂综合征(APS)。患者在接种疫苗后两个月内未能产生抗尖峰蛋白 IgG 抗体。通过血浆置换、抗凝和免疫抑制阻止了疾病进展。我们的结论是,疫苗的 RNA 分子可能会诱发系统性红斑狼疮,表现为 APS、低温球蛋白血症、低补体血症和数字坏死。
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