Viruses (Sep 2021)

Kinetics of Nucleocapsid, Spike and Neutralizing Antibodies, and Viral Load in Patients with Severe COVID-19 Treated with Convalescent Plasma

  • Thomas P. Thomopoulos,
  • Margherita Rosati,
  • Evangelos Terpos,
  • Dimitris Stellas,
  • Xintao Hu,
  • Sevasti Karaliota,
  • Anthi Bouchla,
  • Ioannis Katagas,
  • Anastasia Antoniadou,
  • Andreas Mentis,
  • Sotirios G. Papageorgiou,
  • Marianna Politou,
  • Jenifer Bear,
  • Duncan Donohue,
  • Anastasia Kotanidou,
  • Ioannis Kalomenidis,
  • Eleni Korompoki,
  • Robert Burns,
  • Maria Pagoni,
  • Elisavet Grouzi,
  • Stavroula Labropoulou,
  • Kostantinos Stamoulis,
  • Aristotelis Bamias,
  • Sotirios Tsiodras,
  • Meletios-Athanasios Dimopoulos,
  • George N. Pavlakis,
  • Vasiliki Pappa,
  • Barbara K. Felber

DOI
https://doi.org/10.3390/v13091844
Journal volume & issue
Vol. 13, no. 9
p. 1844

Abstract

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COVID-19 is an ongoing pandemic with high morbidity and mortality. Despite meticulous research, only dexamethasone has shown consistent mortality reduction. Convalescent plasma (CP) infusion might also develop into a safe and effective treatment modality on the basis of recent studies and meta-analyses; however, little is known regarding the kinetics of antibodies in CP recipients. To evaluate the kinetics, we followed 31 CP recipients longitudinally enrolled at a median of 3 days post symptom onset for changes in binding and neutralizing antibody titers and viral loads. Antibodies against the complete trimeric Spike protein and the receptor-binding domain (Spike-RBD), as well as against the complete Nucleocapsid protein and the RNA binding domain (N-RBD) were determined at baseline and weekly following CP infusion. Neutralizing antibody (pseudotype NAb) titers were determined at the same time points. Viral loads were determined semi-quantitatively by SARS-CoV-2 PCR. Patients with low humoral responses at entry showed a robust increase of antibodies to all SARS-CoV-2 proteins and Nab, reaching peak levels within 2 weeks. The rapid increase in binding and neutralizing antibodies was paralleled by a concomitant clearance of the virus within the same timeframe. Patients with high humoral responses at entry demonstrated low or no further increases; however, virus clearance followed the same trajectory as in patients with low antibody response at baseline. Together, the sequential immunological and virological analysis of this well-defined cohort of patients early in infection shows the presence of high levels of binding and neutralizing antibodies and potent clearance of the virus.

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