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Appropriate vaccination remains the most effective approach against contracting the severe acute respiratory syndrome coronavirus 2 infection and the resulting coronavirus disease 2019 (COVID-19) [1, 2]. Although most adverse events due to both adenoviral vector-based (ChAdOx1 nCov-19 and Ad26.COV2.S) and mRNA-based (BNT162b2 mRNA and mRNA-1273) vaccines are tolerable, thrombotic thrombocytopenic purpura (TTP) is a rare but potentially fatal event [3, 4]. Herein, we present the case of a patient with ChAdOx1 nCov-19 vaccine-induced TTP successfully treated with plasmapheresis.
A 75-year-old man experienced bleeding from the tongue 30 days after administration of the ChAdOx1 nCov-19 vaccine. His initial hemogram revealed leukocytosis (leukocyte count: 9520/μL; reference: 4000–8000/μL), anemia (hemoglobin: 10.5 g/dL; reference: 13.5–17.5 g/dL), and thrombocytopenia (platelet: 9000/μL; reference: 150000–400000/μL). Furthermore, increased d-dimer (2.74 mg/FEU; reference: < 0.55 mg/FEU) and lactate dehydrogenase (1675 IU/L; reference: 120–240 IU/L) levels and decreased haptoglobin (< 0.0781 g/L; reference: 0.3–2.0 g/L) levels were noted. Prothrombin time, activated partial thromboplastin time, and fibrinogen level were within normal ranges. To further investigate the possibility of vaccine-induced immune thrombotic thrombocytopenia, we performed the enzyme-linked immunosorbent assay to detect antibodies against the PF4-heparin/complex, which tested negative (optical density: 0.127; reference: < 0.400). Multidetector computed tomography did not reveal peripheral vascular or pulmonary artery thrombosis. Autoimmune panel workup was unremarkable. Human immunodeficiency virus, hepatitis B virus, Epstein–Barr virus, and cytomegalovirus all tested negative. However, we found abundant schistocytes on the peripheral blood smear (Fig. 1a), and the ADAMTS-13 activity was only 0.8% (reference: 40–130%). Considering TTP, we initiated plasmapheresis for five consecutive days. Thrombocytopenia substantially improved from 9000 to 235000/μL (Fig. 1b).
Although cases of TTP after various vaccinations have been previously reported [5], the pathophysiology of the ChAdOx1 nCov-19 vaccine-induced TTP remains unclear. Autoantibodies against ADAMTS-13 induced by the ChAdOx1 nCov-19 vaccine could be a potential mechanism [3]. In addition to vaccine-induced immune thrombotic thrombocytopenia [6], TTP needs to be considered in patients presenting with thrombocytopenia after any COVID-19 vaccination. Early diagnosis and plasmapheresis are crucial to prevent mortality in these patients.
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This study was partially supported by grants from MOST 110-2314-B-075A-005
TCVGH-1103701C.
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This study was conducted in accordance with the current version of the Declaration of Helsinki. The institutional review board of the Taichung Veterans General Hospital approved the study and agreed to waive the patient’s informed consent due to its retrospective nature (CE21356B).
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Chieh-Lin Jerry Teng received an honorarium and consulting fees from Novartis, Roche, Takeda, Johnson & Johnson, Amgen, BMS Celgene, Kirin, AbbVie, and MSD. The other authors declare that they have no conflicts of interest.
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Wang, YC., Chen, TC., Teng, CL.J. et al. ChAdOx1 nCov-19 vaccine-induced thrombotic thrombocytopenic purpura successfully treated with plasmapheresis. Ann Hematol 101, 1123–1124 (2022). https://doi.org/10.1007/s00277-021-04701-x
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DOI: https://doi.org/10.1007/s00277-021-04701-x