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Potential Anionic Substances Binding to Platelet Factor 4 in Vaccine-Induced Thrombotic Thrombocytopenia of ChAdOx1-S Vaccine for SARS-CoV-2
- Source :
- Frontiers in Immunology, Vol 12 (2022), Frontiers in Immunology
- Publication Year :
- 2022
- Publisher :
- Frontiers Media S.A., 2022.
-
Abstract
- Recent reports of rare ChAdOx1-S vaccine-related venous thrombosis led to the suspension of its usage in several countries. Vaccine-induced thrombotic thrombocytopenia (VITT) is characterized by thrombocytopenia and thrombosis in association with anti-platelet factor 4 (PF4) antibodies. Herein, we propose five potential anionic substances of the ChAdOx1-S vaccine that can combine with PF4 and trigger VITT, including (1) the proteins on the surface of adenovirus, e.g., negative charged glycoprotein, (2) the adjuvant components of the vaccine, e.g., Tween 80, (3) the DNA of adenovirus, (4) the S protein antigen expressed by the vaccine, and (5) the negatively charged impurity proteins expressed by the vaccine, e.g., adenovirus skeleton proteins. After analysis of each case, we consider the most possible trigger to be the negatively charged impurity proteins expressed by the vaccine. Then, we display the possible extravascular route and intravascular route of the formation of PF4 autoantibodies triggered by the negatively charged impurity proteins, which is accordant with the clinical situation. Accordingly, the susceptible individuals of VITT after ChAdOx1-S vaccination may be people who express negatively charged impurity proteins and reach a certain high titer.
- Subjects :
- SARS-CoV-2
Vaccination
Immunology
COVID-19
Thrombosis
vaccine-induced thrombotic thrombocytopenia (VITT)
RC581-607
Antibodies, Viral
Platelet Factor 4
Thrombocytopenia
ChAdOx1-S vaccine
PF4
Adjuvants, Immunologic
Adenovirus Vaccines
ChAdOx1 nCoV-19
Hypothesis and Theory
Spike Glycoprotein, Coronavirus
Humans
Immunology and Allergy
Immunologic diseases. Allergy
anionic substances
Subjects
Details
- Language :
- English
- ISSN :
- 16643224
- Volume :
- 12
- Database :
- OpenAIRE
- Journal :
- Frontiers in Immunology
- Accession number :
- edsair.doi.dedup.....c5172578c7a27d42771453d49c33fc5e
- Full Text :
- https://doi.org/10.3389/fimmu.2021.782335/full