Summary of Study ST002477

This data is available at the NIH Common Fund's National Metabolomics Data Repository (NMDR) website, the Metabolomics Workbench, https://www.metabolomicsworkbench.org, where it has been assigned Project ID PR001600. The data can be accessed directly via it's Project DOI: 10.21228/M8W70C This work is supported by NIH grant, U2C- DK119886.

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This study contains a large results data set and is not available in the mwTab file. It is only available for download via FTP as data file(s) here.

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Study IDST002477
Study TitleNeutrophil metabolomics in COVID-19
Study SummarySevere COVID-19 is characterized by an increase in the number and changes in the function of innate immune cells including neutrophils. However, it is not known how the metabolome of immune cells changes in COVID-19 patients or how metabolic changes may contribute to immune dysfunction. To address these questions, we analyzed the metabolome of neutrophils from patients with severe or mild COVID-19, or healthy controls. We identified widespread dysregulation of neutrophil metabolism with disease progression including in amino acid, redox, and central carbon metabolism.
Institute
UT Southwestern Medical Center
Last NameLi
First NameYafeng
Address5323 Harry Hines Blvd, Children's Research Institute, Dallas, TX, 75309, USA
Emailyafeng.li@utsouthwestern.edu
Phone4047696693
Submit Date2023-02-14
Raw Data AvailableYes
Raw Data File Type(s)mzXML, raw(Thermo)
Analysis Type DetailLC-MS
Release Date2023-02-26
Release Version1
Yafeng Li Yafeng Li
https://dx.doi.org/10.21228/M8W70C
ftp://www.metabolomicsworkbench.org/Studies/ application/zip

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Project:

Project ID:PR001600
Project DOI:doi: 10.21228/M8W70C
Project Title:Human neutrophil metabolomics
Project Type:MS qualitative analysis
Project Summary:Severe COVID-19 is characterized by an increase in the number and changes in the function of innate immune cells including neutrophils. However, it is not known how the metabolome of immune cells changes in COVID-19 patients or how metabolic changes may contribute to immune dysfunction. To address these questions, we analyzed the metabolome of neutrophils from patients with severe or mild COVID-19, or healthy controls. We identified widespread dysregulation of neutrophil metabolism with disease progression including in amino acid, redox, and central carbon metabolism.
Institute:UT Southwestern Medical Center
Department:Children's Research Institute
Last Name:Li
First Name:Yafeng
Address:5323 Harry Hines Blvd, Children's Research Institute, Dallas, TX, 75309, USA
Email:yafeng.li@utsouthwestern.edu
Phone:4047696693
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