TY - JOUR
AU - Baker, Alexander T.
AU - Boyd, Ryan J.
AU - Sarkar, Daipayan
AU - Teijeira-Crespo, Alicia
AU - Chan, Chun Kit
AU - Bates, Emily
AU - Waraich, Kasim
AU - Vant, John
AU - Wilson, Eric
AU - Truong, Chloe D.
AU - Lipka-Lloyd, Magdalena
AU - Fromme, Petra
AU - Vermaas, Josh
AU - Williams, Dewight
AU - Machiesky, LeeAnn
AU - Heurich, Meike
AU - Nagalo, Bolni M.
AU - Coughlan, Lynda
AU - Umlauf, Scott
AU - Chiu, Po-Lin
AU - Rizkallah, Pierre J.
AU - Cohen, Taylor S.
AU - Parker, Alan L.
AU - Singharoy, Abhishek
AU - Borad, Mitesh J.
PY - 2021
DA - December
TI - ChAdOx1 interacts with CAR and PF4 with implications for thrombosis with thrombocytopenia syndrome
JO - Science Advances
VL - 7
IS - 49
DO - https://doi.org/10.1126/sciadv.abl8213
AB - Vaccines derived from chimpanzee adenovirus Y25 (ChAdOx1), human adenovirus type 26 (HAdV-D26), and human adenovirus type 5 (HAdV-C5) are critical in combatting the severe acute respiratory coronavirus 2 (SARS-CoV-2) pandemic. As part of the largest vaccination campaign in history, ultrarare side effects not seen in phase 3 trials, including thrombosis with thrombocytopenia syndrome (TTS), a rare condition resembling heparin-induced thrombocytopenia (HIT), have been observed. This study demonstrates that all three adenoviruses deployed as vaccination vectors versus SARS-CoV-2 bind to platelet factor 4 (PF4), a protein implicated in the pathogenesis of HIT. We have determined the structure of the ChAdOx1 viral vector and used it in state-of-the-art computational simulations to demonstrate an electrostatic interaction mechanism with PF4, which was confirmed experimentally by surface plasmon resonance. These data confirm that PF4 is capable of forming stable complexes with clinically relevant adenoviruses, an important step in unraveling the mechanisms underlying TTS. Abstract INTRODUCTION RESULTS DISCUSSION MATERIALS AND METHODS Acknowledgments Supplementary Materials REFERENCES AND NOTES 0eLetters Abstract Vaccines derived from chimpanzee adenovirus Y25 (ChAdOx1), human adenovirus type 26 (HAdV-D26), and human adenovirus type 5 (HAdV-C5) are critical in combatting the severe acute respiratory coronavirus 2 (SARS-CoV-2) pandemic. As part of the largest vaccination campaign in history, ultrarare side effects not seen in phase 3 trials, including thrombosis with thrombocytopenia syndrome (TTS), a rare condition resembling heparin-induced thrombocytopenia (HIT), have been observed. This study demonstrates that all three adenoviruses deployed as vaccination vectors versus SARS-CoV-2 bind to platelet factor 4 (PF4), a protein implicated in the pathogenesis of HIT. We have determined the structure of the ChAdOx1 viral vector and used it in state-of-the-art computational simulations to demonstrate an electrostatic interaction mechanism with PF4, which was confirmed experimentally by surface plasmon resonance. These data confirm that PF4 is capable of forming stable complexes with clinically relevant adenoviruses, an important step in unraveling the mechanisms underlying TTS.
PB - American Association for the Advancement of Science
UR - http://eprints.gla.ac.uk/259937/
KW - Coronavirus (COVID-19)
ER