Publication
Immunophenotyping assessment in a COVID-19 cohort (IMPACC): A prospective longitudinal study
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- Persistent URL
- Last modified
- 06/25/2025
- Type of Material
- Authors
- Language
- English
- Date
- 2021-08-01
- Publisher
- AMER ASSOC ADVANCEMENT SCIENCE
- Publication Version
- Copyright Statement
- © 2021 The Authors, some rights reserved; exclusive licensee American Association for the Advancement of Science. No claim to original U.S.Government Works.
- License
- Final Published Version (URL)
- Title of Journal or Parent Work
- Volume
- 6
- Issue
- 62
- Grant/Funding Information
- This study is being supported by grants R01AI104870, R01AI132774, R01AI135803, R01AI145835, U19AI057229, U19AI062629, U19AI077439, U19AI089992, U19AI090023, U19AI118608, U19AI118610, U19AI125357, U19AI128910, U19AI128913, U54AI142766, U19AI089992, and U24AI52179 from the National Institute of Allergy and Infectious Diseases (NIAID), a part of the U.S. National Institutes of Health (NIH), and P51 OD011132, S10 OD026799 from NIH. The Precision Vaccines Program is supported, in part, by the Department of Pediatrics and Chief Scientific Officer of Boston Children’s Hospital.
- Abstract
- The IMmunoPhenotyping Assessment in a COVID-19 Cohort (IMPACC) is a prospective longitudinal study designed to enroll 1000 hospitalized patients with COVID-19 (NCT04378777). IMPACC collects detailed clinical, laboratory and radiographic data along with longitudinal biologic sampling of blood and respiratory secretions for in depth testing. Clinical and lab data are integrated to identify immunologic, virologic, proteomic, metabolomic and genomic features of COVID-19-related susceptibility, severity and disease progression. The goals of IMPACC are to better understand the contributions of pathogen dynamics and host immune responses to the severity and course of COVID-19 and to generate hypotheses for identification of biomarkers and effective therapeutics, including optimal timing of such interventions. In this report we summarize the IMPACC study design and protocols including clinical criteria and recruitment, multi-site standardized sample collection and processing, virologic and immunologic assays, harmonization of assay protocols, high-level analyses and the data sharing plans.
- Author Notes
- Keywords
- Research Categories
- Health Sciences, Immunology
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