Comparative analysis of antibodies to SARS-CoV-2 between asymptomatic and convalescent patients

Connor J. Dwyer, Colleen A. Cloud, Cindy Wang, Philip Heidt, Paramita Chakraborty, Tara F. Duke, Shannon McGue, Braxton Jeffcoat, Jaclyn Dunne, Logan Johnson, Seungho Choi, Georges J. Nahhas, Amy S. Gandy, Nikolina Babic, Frederick S. Nolte, Philip Howe, Besim Ogretmen, Vamsi K. Gangaraju, Stephen Tomlinson, Brian MaddenTracy Bridges, Patrick A. Flume, John Wrangle, Mark P. Rubinstein, Prabhakar K. Baliga, Satish N. Nadig*, Shikhar Mehrotra*

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

10 Scopus citations

Abstract

The SARS-CoV-2 viral pandemic has induced a global health crisis, which requires more in-depth investigation into immunological responses to develop effective treatments and vaccines. To understand protective immunity against COVID-19, we screened over 60,000 asymptomatic individuals in the Southeastern United States for IgG antibody positivity against the viral Spike protein, and approximately 3% were positive. Of these 3%, individuals with the highest anti-S or anti-RBD IgG level showed a strong correlation with inhibition of ACE2 binding and cross-reactivity against non-SARS-CoV-2 coronavirus S-proteins. We also analyzed samples from 94 SARS-CoV-2 patients and compared them with those of asymptomatic individuals. SARS-CoV-2 symptomatic patients had decreased antibody responses, ACE2 binding inhibition, and antibody cross-reactivity. Our study shows that healthy individuals can mount robust immune responses against SARS-CoV-2 without symptoms. Furthermore, IgG antibody responses against S and RBD may correlate with high inhibition of ACE2 binding in individuals tested for SARS-CoV-2 infection or post vaccination.

Original languageEnglish (US)
Article number102489
JournaliScience
Volume24
Issue number6
DOIs
StatePublished - Jun 25 2021

Funding

The work was supported in part by NIH grants R01CA138930 , R01CA250458 , R01DE030013 , R41CA239952 ; South Carolina Clinical & Translational Research ( SCTR ) award 2104 to S.M.; and P01CA203628 to B.O. R01CA222817 and SCTR award 2017 to M.P.R. and J.W. also supported this work. Support from MUSC President's Office for COVID-19 Research and Hollings Cancer Center Shared Resources (partly supported by P30 CA138313 ) at MUSC is also acknowledged.

Keywords

  • Immunology
  • Infection control in health technology
  • Virology

ASJC Scopus subject areas

  • General

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