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Development of flow cytometry-based assays to assess the ability of antibodies to bind to SARS-CoV-2-infected and spike-transfected cells and mediate NK cell degranulation.

Publication ,  Journal Article
Mielke, D; Stanfield-Oakley, S; Jha, S; Keyes, T; Zalaquett, A; Dunn, B; Rodgers, N; Oguin, T; Sempowski, GD; Binder, RA; Gray, GC; Karuna, S ...
Published in: Cytometry A
June 2022

Since the beginning of the SARS-CoV-2 pandemic, antibody responses and antibody effector functions targeting SARS-CoV-2-infected cells have been understudied. Consequently, the role of these types of antibodies in SARS-CoV-2 disease (COVID-19) and immunity is still undetermined. To provide tools to study these responses, we used plasma from SARS-CoV-2-infected individuals (n = 50) and SARS-CoV-2 naive healthy controls (n = 20) to develop four specific and reproducible flow cytometry-based assays: (i) two assessing antibody binding to, and antibody-mediated NK cell degranulation against, SARS-CoV-2-infected cells and (ii) two assessing antibody binding to, and antibody-mediated NK cell degranulation against, SARS-CoV-2 Spike-transfected cells. All four assays demonstrated the ability to detect the presence of these functional antibody responses in a specific and reproducible manner. Interestingly, we found weak to moderate correlations between the four assays (Spearman rho ranged from 0.50 to 0.74), suggesting limited overlap in the responses captured by the individual assays. Lastly, while we initially developed each assay with multiple dilutions in an effort to capture the full relationship between antibody titers and assay outcome, we explored the relationship between fewer antibody dilutions and the full dilution series for each assay to reduce assay costs and improve assay efficiency. We found high correlations between the full dilution series and fewer or single dilutions of plasma. Use of single or fewer sample dilutions to accurately determine the response rates and magnitudes of the responses allows for high-throughput use of these assays platforms to facilitate assessment of antibody responses elicited by SARS-CoV-2 infection and vaccination in large clinical studies.

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Published In

Cytometry A

DOI

EISSN

1552-4930

Publication Date

June 2022

Volume

101

Issue

6

Start / End Page

483 / 496

Location

United States

Related Subject Headings

  • Spike Glycoprotein, Coronavirus
  • SARS-CoV-2
  • Immunology
  • Humans
  • Flow Cytometry
  • Cell Degranulation
  • COVID-19
  • Antibodies, Viral
  • 3201 Cardiovascular medicine and haematology
  • 0601 Biochemistry and Cell Biology
 

Citation

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Mielke, D., Stanfield-Oakley, S., Jha, S., Keyes, T., Zalaquett, A., Dunn, B., … Ferrari, G. (2022). Development of flow cytometry-based assays to assess the ability of antibodies to bind to SARS-CoV-2-infected and spike-transfected cells and mediate NK cell degranulation. Cytometry A, 101(6), 483–496. https://doi.org/10.1002/cyto.a.24552
Mielke, Dieter, Sherry Stanfield-Oakley, Shalini Jha, Taylor Keyes, Adam Zalaquett, Brooke Dunn, Nicole Rodgers, et al. “Development of flow cytometry-based assays to assess the ability of antibodies to bind to SARS-CoV-2-infected and spike-transfected cells and mediate NK cell degranulation.Cytometry A 101, no. 6 (June 2022): 483–96. https://doi.org/10.1002/cyto.a.24552.
Mielke, Dieter, et al. “Development of flow cytometry-based assays to assess the ability of antibodies to bind to SARS-CoV-2-infected and spike-transfected cells and mediate NK cell degranulation.Cytometry A, vol. 101, no. 6, June 2022, pp. 483–96. Pubmed, doi:10.1002/cyto.a.24552.
Mielke D, Stanfield-Oakley S, Jha S, Keyes T, Zalaquett A, Dunn B, Rodgers N, Oguin T, Sempowski GD, Binder RA, Gray GC, Karuna S, Corey L, Hural J, Tomaras GD, Pollara J, Ferrari G. Development of flow cytometry-based assays to assess the ability of antibodies to bind to SARS-CoV-2-infected and spike-transfected cells and mediate NK cell degranulation. Cytometry A. 2022 Jun;101(6):483–496.
Journal cover image

Published In

Cytometry A

DOI

EISSN

1552-4930

Publication Date

June 2022

Volume

101

Issue

6

Start / End Page

483 / 496

Location

United States

Related Subject Headings

  • Spike Glycoprotein, Coronavirus
  • SARS-CoV-2
  • Immunology
  • Humans
  • Flow Cytometry
  • Cell Degranulation
  • COVID-19
  • Antibodies, Viral
  • 3201 Cardiovascular medicine and haematology
  • 0601 Biochemistry and Cell Biology