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SARS-CoV-2 Vaccine Improved Hemostasis of a Patient with Protein S Deficiency: A Case Report
Mohammad A Mohammad1, Alaa Malik1, Lekha Thangada1
1Department of Interdisciplinary Oncology, Louisiana State University Health Sciences Center (LSUHSC), New Orleans, LA 70112, USA.
Insights
COVID-19 vaccination may reduce thrombosis risk in individuals with inherited thrombophilia. A patient with Protein S deficiency showed improved clotting parameters after vaccination, suggesting a potential therapeutic benefit.
Area of Science:
- Genetics and Thrombosis
- Immunology and Vaccination
Background:
- A 16-year-old female presented with neonatal stroke and hemiparesis, later diagnosed with a missense mutation in the PROS1 gene, causing hereditary Protein S deficiency.
- The patient's family history revealed Protein S deficiency in her father and paternal grandfather, confirming an inherited thrombophilia.
Observation:
- Plasma analysis at age 13 indicated low Protein S activity and prolonged clotting time, consistent with the PROS1 gene mutation.
- Following COVID-19 vaccination (Pfizer, 2021-2022), the patient's plasma samples collected 8 weeks post-immunization demonstrated improved clotting parameters for up to 6 months.
Findings:
- Post-vaccination plasma showed a significant reduction in thrombin generation and improved activated partial thromboplastin time (aPTT) clotting time.
- Mass spectrometry revealed increased antithrombin-III and decreased thrombin and FXII levels after vaccination compared to her father.
Implications:
- This case report is the first to suggest that COVID-19 vaccination may lower thrombosis risk in a patient with inherited thrombophilia due to Protein S deficiency.
- Further research is warranted to explore the impact of COVID-19 vaccinations on other forms of inherited thrombophilia and their associated mutations.
Abstract:
A 16-year-old patient, while an infant, incurred right-sided hemiparesis and had difficulty breast feeding. She was later diagnosed with a neonatal stroke and her genetic testing showed a missense mutation in her PROS1 (Protein S) gene. Both her grandfather and father, but not her mother, had hereditary Protein S (PS) deficiency. The patient was not prescribed any mediation due to her young age but was frequently checked by her physician. The patient's plasma was first collected at the age of 13, and the isolated plasma from the patient and her father were analyzed by aPTT, thrombin generation, and enzyme-linked immunosorbent assays. These analyses showed low PS activity and clotting time associated with the missense mutation in the PROS1 gene. During the COVID-19 pandemic, the patient received her first Pfizer vaccination dose in 2021, followed by a booster dose in 2022. The plasma samples were collected 8 weeks post-immunization, after which her clotting parameters had improved for up to 6 months following vaccination. The patient's plasma showed a significant reduction in thrombin generation and an improved aPTT clotting time. Mass spectrometry analysis revealed that her antithrombin-III level was significantly higher post-vaccination, and both thrombin and FXII levels were significantly lowered compared with her father. To our knowledge, this is the first report to document that COVID-19 vaccination can lower the risk of thrombosis in a patient with inherited thrombophilia. Although the effect was observed on a single mutation, it would be interesting to investigate the effect of COVID-19 vaccinations on other thrombophilia.
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