Data from: A longitudinal assessment of the antibody response to SARS-CoV-2 infection in the New Mexican population
Data files
Dec 04, 2025 version files 42.80 KB
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Figure_1_data.xlsx
9.99 KB
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Figure_2_data_revised.xlsx
9.63 KB
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Figure_3_data_revised.xlsx
9.64 KB
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Figure_4_data_revised.xlsx
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README.md
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Abstract
While many studies have assessed immune responses to SARS-CoV-2 infection, none have studied functional antibody responses before and after vaccination of exposed patients in New Mexico in the United States. Here, we evaluate antibody binding, antibody neutralization, and antibody-dependent cell-mediated cytotoxicity (ADCC) responses from convalescent patients between 2020 and 2021. Our results indicate that binding, neutralizing, and ADCC titers remained durable over an estimated 4-month period or were boosted by vaccination. Antibody binding titer stability was comparable to that of antibodies against four common viruses. Overall, these data shed light on functional antibody responses to SARS-CoV-2 in pre-alpha variant waves in New Mexico.
Dataset DOI: 10.5061/dryad.905qfttx3
Description of the data and file structure
These experiments were conducted to assess antibody responses (binding, functional, and neutralizing) against SARS-CoV-2 in 2020-2021 in New Mexican patients and to assess the effect of vaccination on pre-existing antibody titers. All missing values are represented as N/A.
Files and variables
File: Figure_1_data.xlsx
Description:
- Column A: patient number
- Column B: ELISA titers agaSARS-CoV-2CoV-2 from the first blood draw of unvaccinated patients
- Column C: ELISA titers againSARS-CoV-2V-2 from the second blood draw of unvaccinated patients
- Column D: ELISA titers agaSARS-CoV-2CoV-2 from the first blood draw of unvaccinated patients that were later vaccinated
- Column E: ELISA titers against SARS-CoV-22 from the second blood draw of patients who were vaccinated between draws 1 and 2
IgG concentrations were calculated utilizing the trendline equation created using the standard’s included in the kit.
File: Figure_2_data_revised.xlsx
Description:
- Column A: patient number
- Column B: Fold change in ELISA titers against SARS-CoV-2 between blood draws 1 and 2
- Column C: Fold change in ELISA titers against adenovirus between blood draws 1 and 2
- Column D: Fold change in ELISA titers against cytomegalovirus between blood draws 1 and 2
- Column E: Fold change in ELISA titers against measles virus between blood draws 1 and 2
- Column F: Fold change in ELISA titers against common cold coronavirus hCoV 299E between blood draws 1 and 2
Fold change in IgG concentration between draw 1 and draw 2 was calculated for each patient.
File: Figure_3_data_revised.xlsx
Description:
- Column A: patient number
- Column B: neutralizing antibody titers agaiSARS-CoV-2oV-2 from the first blood draw of unvaccinated patients
- Column C: neutralizing antibody titers agaSARS-CoV-2CoV-2 from the second blood draw of unvaccinated patients
- Column D: neutralizing antibody titers against agSARS-CoV-2 CoV-2 from the first blood draw of unvaccinated patients that were later vaccinated
- Column E: neutralizing antibody titers against agSARS-CoV-2 CoV-2 from the second blood draw of patients who were vaccinated between draws 1 and 2
Neutralization of SARS-CoV-2 live virus was assessed through a PRNT.
File: Figure_4_data_revised.xlsx
Description:
- Column A: patient number
- Column B: antibody-dependent cell-mediated cytotoxicity (ADCC) titers agaiSARS-CoV-2oV-2 from the first blood draw of unvaccinated patients
- Column C: antibody-dependent cell-mediated cytotoxicity titers against againsSARS-CoV-2-2 from the second blood draw of unvaccinated patients
- Column D: antibody-dependent cell-mediated cytotoxicity titers against SARS-CoV-22 from the first blood draw of unvaccinated patients who were later vaccinated
- Column E: antibody-dependent cell-mediated cytotoxicity titers against agSARS-CoV-2 CoV-2 from the second blood draw of patients who were vaccinated between draws 1 and 2
ADCC activity was assessed using an ADCC luciferase reporter assay.
Code/software
Data are Excel worksheets
Access information
Other publicly accessible locations of the data:
- None
Data was derived from the following sources:
- None
Human subjects data
We received explicit informed consent from the study participants to publish de-identified data in the public domain. The data was de-identified by blinding experimentalists from PHI and assigning a anonymized number to each patient.
