Go to The Journal of Clinical Investigation
  • About
  • Editors
  • Consulting Editors
  • For authors
  • Publication ethics
  • Transfers
  • Advertising
  • Job board
  • Contact
  • Current issue
  • Past issues
  • By specialty
    • COVID-19
    • Cardiology
    • Immunology
    • Metabolism
    • Nephrology
    • Oncology
    • Pulmonology
    • All ...
  • Videos
  • Collections
    • Resource and Technical Advances
    • Clinical Medicine
    • Reviews
    • Editorials
    • Perspectives
    • Top read articles
  • JCI This Month
    • Current issue
    • Past issues

  • Current issue
  • Past issues
  • Specialties
  • In-Press Preview
  • Concise Communication
  • Editorials
  • Viewpoint
  • Top read articles
  • About
  • Editors
  • Consulting Editors
  • For authors
  • Publication ethics
  • Transfers
  • Advertising
  • Job board
  • Contact
Heterogeneous antibodies against SARS-CoV-2 spike receptor binding domain and nucleocapsid with implications for COVID-19 immunity
Kathleen M. McAndrews, … , James P. Allison, Raghu Kalluri
Kathleen M. McAndrews, … , James P. Allison, Raghu Kalluri
Published August 14, 2020
Citation Information: JCI Insight. 2020;5(18):e142386. https://doi.org/10.1172/jci.insight.142386.
View: Text | PDF
Research Article COVID-19 Immunology

Heterogeneous antibodies against SARS-CoV-2 spike receptor binding domain and nucleocapsid with implications for COVID-19 immunity

  • Text
  • PDF
Abstract

Evaluation of potential immunity against the novel severe acute respiratory syndrome (SARS) coronavirus that emerged in 2019 (SARS-CoV-2) is essential for health, as well as social and economic recovery. Generation of antibody response to SARS-CoV-2 (seroconversion) may inform on acquired immunity from prior exposure, and antibodies against the SARS-CoV-2 spike protein receptor binding domain (S-RBD) are speculated to neutralize virus infection. Some serology assays rely solely on SARS-CoV-2 nucleocapsid protein (N-protein) as the antibody detection antigen; however, whether such immune responses correlate with S-RBD response and COVID-19 immunity remains unknown. Here, we generated a quantitative serological ELISA using recombinant S-RBD and N-protein for the detection of circulating antibodies in 138 serial serum samples from 30 reverse transcription PCR–confirmed, SARS-CoV-2–hospitalized patients, as well as 464 healthy and non–COVID-19 serum samples that were collected between June 2017 and June 2020. Quantitative detection of IgG antibodies against the 2 different viral proteins showed a moderate correlation. Antibodies against N-protein were detected at a rate of 3.6% in healthy and non–COVID-19 sera collected during the pandemic in 2020, whereas 1.9% of these sera were positive for S-RBD. Approximately 86% of individuals positive for S-RBD–binding antibodies exhibited neutralizing capacity, but only 74% of N-protein–positive individuals exhibited neutralizing capacity. Collectively, our studies show that detection of N-protein–binding antibodies does not always correlate with presence of S-RBD–neutralizing antibodies and caution against the extensive use of N-protein–based serology testing for determination of potential COVID-19 immunity.

Authors

Kathleen M. McAndrews, Dara P. Dowlatshahi, Jianli Dai, Lisa M. Becker, Janine Hensel, Laura M. Snowden, Jennifer M. Leveille, Michael R. Brunner, Kylie W. Holden, Nikolas S. Hopkins, Alexandria M. Harris, Jerusha Kumpati, Michael A. Whitt, J. Jack Lee, Luis L. Ostrosky-Zeichner, Ramesha Papanna, Valerie S. LeBleu, James P. Allison, Raghu Kalluri

×

Figure 3

Seroconversion in patients with COVID-19 and clinical outcomes.

Options: View larger image (or click on image) Download as PowerPoint
Seroconversion in patients with COVID-19 and clinical outcomes.
(A) Corr...
(A) Correlation (Spearman’s correlation coefficient r displayed) contrasting the normalized A450 values from the last or only serum sample analyzed for S-RBD and N-protein. n = 37 serum samples (from 21 patients with SARS-CoV-2). (B) Heatmap depicting positive, low titer positive, or negative categorization of the last or only serum sample for each patient and for each viral protein tested. Case numbers are color-coded: green: recovered, blue: hospitalized, red: deceased. Low titer positive as defined by detecting of binding antibodies shown in Supplemental Figure 4, D and E, 1:20 titer. (C) Normalized S-RBD (top panels), and N-protein (bottom panels) absorbance for patients classified based on their current status (recovered, green; hospitalized, blue; deceased, red). Data are reported as mean ± standard deviation (SD) of 3 technical replicates for each sample. The first (or only) and most recent serum samples are shown. NC (line), negative control cutoff (see Methods); HS, healthy samples from 2017 to 2020 (n = 412 for S-RBD; n = 411 for N-protein).

Copyright © 2022 American Society for Clinical Investigation
ISSN 2379-3708

Sign up for email alerts