Anti-SARS-CoV-2 Spike Protein and Anti-Platelet Factor 4 Antibody Responses Induced by COVID-19 Disease and ChAdOx1 nCov-19 vaccination

Author:

Greinacher Andreas1,Selleng Kathleen1,Mayerle Julia2,Palankar Raghavendra1,Wesche Jan1,Reiche Sven3,Aebischer Andrea3,Warkentin Theodore E.4,Muenchhoff Maximilian5,Hellmuth Johannes C.6,Keppler Oliver T.5,Duerschmied Daniel7,Lother Achim7,Rieg Siegbert7,Gawaz Meinrad Paul8,Mueller Karin Anne Lydia8,Scheer Christian S.1,Napp Matthias1,Hahnenkamp Klaus1,Lucchese Guglielmo1,Vogelgesang Antje1,Flöel Agnes1,Lovreglio Piero9,Stufano Angela9,Marschalek Rolf10,Thiele Thomas1

Affiliation:

1. University Medicine Greifswald

2. German Centre for Infection Research (DZIF)

3. Friedrich-Loeffler Institut, Greifswald-Insel Riems

4. McMaster University

5. Ludwig Maximilians University of Munich

6. University Hospital Munich

7. University of Freiburg

8. University Tuebingen

9. University of Bari

10. Goethe University

Abstract

Abstract Background: Some recipients of ChAdOx1 nCoV-19 COVID-19 Vaccine AstraZeneca develop antibody-mediated vaccine-induced thrombotic thrombocytopenia (VITT), associated with cerebral venous and other unusual thrombosis resembling autoimmune heparin-induced thrombocytopenia. A prothrombotic predisposition is also observed in Covid-19. We explored whether antibodies against the SARS-CoV-2 spike protein induced by Covid-19 cross-react with platelet factor 4 (PF4/CXLC4), the protein targeted in both VITT and autoimmune heparin-induced thrombocytopenia.Methods: Immunogenic epitopes of PF4 and SARS-CoV-2 spike protein were compared via prediction tools and 3D modelling software (IMED, SIM, MacMYPOL). Sera from 222 PCR-confirmed Covid-19 patients from five European centers were tested by PF4/heparin ELISA, heparin-dependent and PF4-dependent platelet activation assays. Immunogenic reactivity of purified anti-PF4 and anti-PF4/heparin antibodies from patients with VITT were tested against recombinant SARS-CoV-2 spike protein. Results: Three motifs within the spike protein sequence share a potential immunogenic epitope with PF4. Nineteen of 222 (8.6%) Covid-19 patient sera tested positive in the IgG-specific PF4/heparin ELISA, none of which showed platelet activation in the heparin-dependent activation assay, including 10 (4.5%) of the 222 Covid-19 patients who developed thromboembolic complications. Purified anti-PF4 and anti-PF4/heparin antibodies from two VITT patients did not show cross-reactivity to recombinant SARS-CoV-2 spike protein. Conclusions: The antibody responses to PF4 in SARS-CoV-2 infection and after vaccination with COVID-19 Vaccine AstraZeneca differ. Antibodies against SARS-CoV-2 spike protein do not cross-react with PF4 or PF4/heparin complexes through molecular mimicry. These findings make it very unlikely that the intended vaccine-induced immune response against SARS-CoV-2 spike protein would itself induce VITT.

Publisher

Research Square Platform LLC

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