Neutralizing Antibody Responses in COVID-19 Convalescent Sera

J Infect Dis. 2021 Jan 4;223(1):47-55. doi: 10.1093/infdis/jiaa673.

Abstract

Passive transfer of antibodies from COVID-19 convalescent patients is being used as an experimental treatment for eligible patients with SARS-CoV-2 infections. The United States Food and Drug Administration's (FDA) guidelines for convalescent plasma initially recommended target antibody titers of 160. We evaluated SARS-CoV-2 neutralizing antibodies in sera from recovered COVID-19 patients using plaque reduction neutralization tests (PRNT) at moderate (PRNT50) and high (PRNT90) stringency thresholds. We found that neutralizing activity significantly increased with time post symptom onset (PSO), reaching a peak at 31-35 days PSO. At this point, the number of sera having neutralizing titers of at least 160 was approximately 93% (PRNT50) and approximately 54% (PRNT90). Sera with high SARS-CoV-2 antibody levels (>960 enzyme-linked immunosorbent assay titers) showed maximal activity, but not all high-titer sera contained neutralizing antibody at FDA recommended levels, particularly at high stringency. These results underscore the value of serum characterization for neutralization activity.

Keywords: COVID-19; SARS-CoV-2; convalescent plasma; neutralizing antibodies.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Antibodies, Neutralizing / blood*
  • Antibodies, Viral / blood*
  • COVID-19 / therapy*
  • COVID-19 Serotherapy
  • Enzyme-Linked Immunosorbent Assay
  • Humans
  • Immunization, Passive
  • Neutralization Tests*

Substances

  • Antibodies, Neutralizing
  • Antibodies, Viral