EBioMedicine (Oct 2024)

Potential immunomodulatory effects of CAS+IMD monoclonal antibody cocktail in hospitalized patients with COVID-19Research in context

  • Bei Wang,
  • Jacquelynn Golubov,
  • Erin M. Oswald,
  • Patrick Poon,
  • Qiaozhi Wei,
  • Clarissa Lett,
  • Fadi Shehadeh,
  • Matthew Kaczynski,
  • Lewis Oscar Felix,
  • Biswajit Mishra,
  • Evangelia K. Mylona,
  • Matthew F. Wipperman,
  • Erica Chio,
  • Sara C. Hamon,
  • Andrea T. Hooper,
  • Selin Somersan-Karakaya,
  • Bret J. Musser,
  • Christopher D. Petro,
  • Jennifer D. Hamilton,
  • Matthew A. Sleeman,
  • George D. Kalliolias,
  • Eleftherios Mylonakis,
  • Dimitris Skokos

Journal volume & issue
Vol. 108
p. 105334

Abstract

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Summary: Background: Passive administration of SARS-CoV-2 neutralizing monoclonal antibodies (mAbs), such as CAS + IMD (Casirivimab + Imdevimab) antibody cocktail demonstrated beneficial effects on clinical outcomes in hospitalized patients with COVID-19 who were seronegative at baseline and outpatients. However, little is known about their impact on the host immunophenotypes. Methods: We conducted an immunoprofiling study in 46 patients from a single site of a multi-site trial of CAS + IMD in hospitalized patients. We collected longitudinal samples during October 2020 ∼ April 2021, prior to the emergence of the Delta and Omicron variants and the use of COVID-19 vaccines. All collected samples were analyzed without exclusion and post-hoc statistical analysis was performed. We examined the dynamic interplay of CAS + IMD with host immunity applying dimensional reduction approach on plasma proteomics and high dimensional flow cytometry data. Findings: Using an unbiased clustering method, we identified unique immunophenotypes associated with acute inflammation and disease resolution. Compared to placebo group, administration of CAS + IMD accelerated the transition from an acute inflammatory immunophenotype, to a less inflammatory or “resolving” immunophenotype, as characterized by reduced tissue injury, proinflammatory markers and restored lymphocyte/monocyte imbalance independent of baseline serostatus. Moreover, CAS + IMD did not impair the magnitude or the quality of host T cell immunity against SARS-CoV-2 spike protein. Interpretation: Our results identified immunophenotypic changes indicative of a possible SARS-CoV-2 neutralizing antibodies-induced anti-inflammatory effect, without an evident impairment of cellular antiviral immunity, suggesting that further studies of Mabs effects on SAS-CoV-2 or other viral mediated inflammation are warranted. Funding: Regeneron Pharmaceuticals Inc and federal funds from the Department of Health and Human Services; Administration for Strategic Preparedness and Response; Biomedical Advanced Research and Development Authority, under OT number: HHSO100201700020C.

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