AI Article Synopsis

  • Recent reports of rare blood clots linked to the ChAdOx1-S vaccine have led to its suspension in some countries due to concerns over vaccine-induced thrombotic thrombocytopenia (VITT).
  • VITT is characterized by low platelet counts and blood clots associated with antibodies that target platelet factor 4 (PF4).
  • The study proposes five potential triggers for VITT related to the vaccine, identifying negatively charged impurity proteins as the most likely cause for the formation of PF4 autoantibodies in susceptible individuals.

Article 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.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC8790015PMC
http://dx.doi.org/10.3389/fimmu.2021.782335DOI Listing

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