NYU Dataset
mRNA COVID-19 vaccine elicits potent adaptive immune response without the acute inflammation of SARS-CoV-2 infection
UID: 10672
- Description
- To investigate immune responses to SARS-CoV-2 antigens under various inflammatory conditions, researchers collected blood samples from five adult patients seen at NYU Langone Health with lab-confirmed cases of acute COVID-19 and from nine healthy adults (seven who had received the BNT162b2 mRNA vaccine and two with no prior exposure to SARS-CoV-2). Samples were obtained at multiple time points. Patients with an active infection contributed longitudinal samples up to 28 days post-onset of symptoms. To assess the vaccine response in healthy patients, samples were collected at baseline and at approximately 1, 3, and 4 weeks after the first vaccine dose. Three of the vaccine recipients also provided samples 5 weeks post-vaccine, pre-booster, and 1 and 4 weeks post-booster. In total, 42 post-vaccination and 9 post-infection samples were collected. These were processed for a total of 195,634 peripheral blood mononuclear cells (PBMC): 36,906 cells (∼19%) from COVID-19 patients; 37,680 cells (∼19%) healthy control and pre-vaccine samples; 90,753 cells (∼46%) from post-vaccine samples; and 30,295 cells (∼15%) from booster samples.
- Geographic Coverage
-
New York (State) - New York City
Homo sapiens
Subject Domain
Population Age
Keywords
Adult (19 years - 64 years)
Senior (65 years - 79 years)
Access
- Restrictions
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Free to All
- Instructions
- Raw and processed sequencing data can be accessed through the CELLxGENE data repository and BioProject collection.
Observational
WHO Clinical Progression Scale
- Grant Support
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LF-OC-20-000351/LEO FoundationR21 AI158997/NIAID NIH
- Other Resources
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COVID-19 Cell Atlas
Haniffa COVID-19 single-cell RNA-seq dataset
IgBLASTA tool for analysis of immunoglobulin (IG) and T cell receptor (TR) V domain sequences
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