TY - JOUR
T1 - COVID-19 Vaccines and Thrombosis—Roadblock or Dead-End Street?
AU - Lundstrom, Kenneth
AU - Barh, Debmalya
AU - Uhal, Bruce D.
AU - Takayama, Kazuo
AU - Aljabali, Alaa A. A.
AU - Abd El-aziz, Tarek Mohamed
AU - Lal, Amos
AU - Redwan, Elrashdy M.
AU - Adadi, Parise
AU - Chauhan, Gaurav
AU - Sherchan, Samendra P.
AU - Azad, Gajendra Kumar
AU - Rezaei, Nima
AU - Serrano-aroca, Ángel
AU - Bazan, Nicolas G.
AU - Hassan, Sk Sarif
AU - Panda, Pritam Kumar
AU - Pal Choudhury, Pabitra
AU - Pizzol, Damiano
AU - Kandimalla, Ramesh
AU - Baetas-da-cruz, Wagner
AU - Mishra, Yogendra Kumar
AU - Palu, Giorgio
AU - Brufsky, Adam M.
AU - Tambuwala, Murtaza M.
AU - Uversky, Vladimir N.
N1 - Publisher Copyright:
© 2021 by the authors. Licensee MDPI, Basel, Switzerland.
PY - 2021/7/13
Y1 - 2021/7/13
N2 - Two adenovirus-based vaccines, ChAdOx1 nCoV-19 and Ad26.COV2.S, and two mRNA-based vaccines, BNT162b2 and mRNA.1273, have been approved by the European Medicines Agency (EMA), and are invaluable in preventing and reducing the incidence of coronavirus disease-2019 (COVID-19). Recent reports have pointed to thrombosis with associated thrombocytopenia as an adverse effect occurring at a low frequency in some individuals after vaccination. The causes of such events may be related to SARS-CoV-2 spike protein interactions with different C-type lectin receptors, heparan sulfate proteoglycans (HSPGs) and the CD147 receptor, or to different soluble splice variants of the spike protein, adenovirus vector interactions with the CD46 receptor or platelet factor 4 antibodies. Similar findings have been reported for several viral diseases after vaccine administration. In addition, immunological mechanisms elicited by viral vectors related to cellular delivery could play a relevant role in individuals with certain genetic backgrounds. Although rare, the potential COVID-19 vaccine-induced immune thrombotic thrombocytopenia (VITT) requires immediate validation, especially in risk groups, such as the elderly, chronic smokers, and individuals with pre-existing incidences of thrombocytopenia; and if necessary, a reformulation of existing vaccines.
AB - Two adenovirus-based vaccines, ChAdOx1 nCoV-19 and Ad26.COV2.S, and two mRNA-based vaccines, BNT162b2 and mRNA.1273, have been approved by the European Medicines Agency (EMA), and are invaluable in preventing and reducing the incidence of coronavirus disease-2019 (COVID-19). Recent reports have pointed to thrombosis with associated thrombocytopenia as an adverse effect occurring at a low frequency in some individuals after vaccination. The causes of such events may be related to SARS-CoV-2 spike protein interactions with different C-type lectin receptors, heparan sulfate proteoglycans (HSPGs) and the CD147 receptor, or to different soluble splice variants of the spike protein, adenovirus vector interactions with the CD46 receptor or platelet factor 4 antibodies. Similar findings have been reported for several viral diseases after vaccine administration. In addition, immunological mechanisms elicited by viral vectors related to cellular delivery could play a relevant role in individuals with certain genetic backgrounds. Although rare, the potential COVID-19 vaccine-induced immune thrombotic thrombocytopenia (VITT) requires immediate validation, especially in risk groups, such as the elderly, chronic smokers, and individuals with pre-existing incidences of thrombocytopenia; and if necessary, a reformulation of existing vaccines.
KW - COVID-19
KW - Humans
KW - Risk Factors
KW - SARS-CoV-2
KW - Smokers
KW - Vaccines
KW - Thrombosis
KW - Chronic smokers
UR - https://www.mdpi.com/2218-273X/11/7/1020
UR - http://www.scopus.com/inward/record.url?scp=85109504294&partnerID=8YFLogxK
U2 - 10.3390/biom11071020
DO - 10.3390/biom11071020
M3 - Article
C2 - 34356644
SN - 2218-273X
VL - 11
JO - Biomolecules
JF - Biomolecules
IS - 7
M1 - 1020
ER -