Frontiers in Immunology (Mar 2022)

Signaling Through FcγRIIA and the C5a-C5aR Pathway Mediate Platelet Hyperactivation in COVID-19

  • Sokratis A. Apostolidis,
  • Sokratis A. Apostolidis,
  • Amrita Sarkar,
  • Heather M. Giannini,
  • Rishi R. Goel,
  • Divij Mathew,
  • Aae Suzuki,
  • Amy E. Baxter,
  • Amy E. Baxter,
  • Allison R. Greenplate,
  • Allison R. Greenplate,
  • Cécile Alanio,
  • Cécile Alanio,
  • Cécile Alanio,
  • Mohamed Abdel-Hakeem,
  • Mohamed Abdel-Hakeem,
  • Derek A. Oldridge,
  • Derek A. Oldridge,
  • Derek A. Oldridge,
  • Josephine R. Giles,
  • Josephine R. Giles,
  • Josephine R. Giles,
  • Jennifer E. Wu,
  • Jennifer E. Wu,
  • Jennifer E. Wu,
  • Zeyu Chen,
  • Zeyu Chen,
  • Yinghui Jane Huang,
  • Yinghui Jane Huang,
  • Jonathan Belman,
  • Jonathan Belman,
  • Ajinkya Pattekar,
  • Ajinkya Pattekar,
  • Sasikanth Manne,
  • Sasikanth Manne,
  • Oliva Kuthuru,
  • Oliva Kuthuru,
  • Jeanette Dougherty,
  • Jeanette Dougherty,
  • Brittany Weiderhold,
  • Ariel R. Weisman,
  • Caroline A. G. Ittner,
  • Sigrid Gouma,
  • Debora Dunbar,
  • Ian Frank,
  • Alexander C. Huang,
  • Alexander C. Huang,
  • Alexander C. Huang,
  • Laura A. Vella,
  • Laura A. Vella,
  • The UPenn COVID Processing Unit,
  • John P. Reilly,
  • Scott E. Hensley,
  • Scott E. Hensley,
  • Lubica Rauova,
  • Lubica Rauova,
  • Liang Zhao,
  • Nuala J. Meyer,
  • Mortimer Poncz,
  • Mortimer Poncz,
  • Charles S. Abrams,
  • E. John Wherry,
  • E. John Wherry,
  • E. John Wherry,
  • E. John Wherry,
  • Sharon Adamski,
  • Zahidul Alam,
  • Mary M. Addison,
  • Katelyn T. Byrne,
  • Aditi Chandra,
  • Hélène C. Descamps,
  • Nicholas Han,
  • Yaroslav Kaminskiy,
  • Shane C. Kammerman,
  • Justin Kim,
  • Jacob T. Hamilton,
  • Nune Markosyan,
  • Julia Han Noll,
  • Dalia K. Omran,
  • Eric Perkey,
  • Elizabeth M. Prager,
  • Dana Pueschl,
  • Austin Rennels,
  • Jennifer B. Shah,
  • Jake S. Shilan,
  • Nils Wilhausen,
  • Ashley N. Vanderbeck

DOI
https://doi.org/10.3389/fimmu.2022.834988
Journal volume & issue
Vol. 13

Abstract

Read online

Patients with COVID-19 present with a wide variety of clinical manifestations. Thromboembolic events constitute a significant cause of morbidity and mortality in patients infected with SARS-CoV-2. Severe COVID-19 has been associated with hyperinflammation and pre-existing cardiovascular disease. Platelets are important mediators and sensors of inflammation and are directly affected by cardiovascular stressors. In this report, we found that platelets from severely ill, hospitalized COVID-19 patients exhibited higher basal levels of activation measured by P-selectin surface expression and had poor functional reserve upon in vitro stimulation. To investigate this question in more detail, we developed an assay to assess the capacity of plasma from COVID-19 patients to activate platelets from healthy donors. Platelet activation was a common feature of plasma from COVID-19 patients and correlated with key measures of clinical outcome including kidney and liver injury, and APACHEIII scores. Further, we identified ferritin as a pivotal clinical marker associated with platelet hyperactivation. The COVID-19 plasma-mediated effect on control platelets was highest for patients that subsequently developed inpatient thrombotic events. Proteomic analysis of plasma from COVID-19 patients identified key mediators of inflammation and cardiovascular disease that positively correlated with in vitro platelet activation. Mechanistically, blocking the signaling of the FcγRIIa-Syk and C5a-C5aR pathways on platelets, using antibody-mediated neutralization, IgG depletion or the Syk inhibitor fostamatinib, reversed this hyperactivity driven by COVID-19 plasma and prevented platelet aggregation in endothelial microfluidic chamber conditions. These data identified these potentially actionable pathways as central for platelet activation and/or vascular complications and clinical outcomes in COVID-19 patients. In conclusion, we reveal a key role of platelet-mediated immunothrombosis in COVID-19 and identify distinct, clinically relevant, targetable signaling pathways that mediate this effect.

Keywords