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Dynamics of SARS-CoV-2 Seroprevalence in a Large US population Over a Period of 12 Months.
Karkanitsa, Maria; Li, Yan; Valenti, Shannon; Spathies, Jacquelyn; Kelly, Sophie; Hunsberger, Sally; Yee, Laura; Croker, Jennifer A; Wang, Jing; Alfonso, Andrea Lucia; Faust, Mondreakest; Mehalko, Jennifer; Drew, Matthew; Denson, John-Paul; Putman, Zoe; Fathi, Parinaz; Ngo, Tran B; Siripong, Nalyn; Baus, Holly Ann; Petersen, Brian; Ford, Eric W; Sundaresan, Vanathi; Josyula, Aditya; Han, Alison; Giurgea, Luca T; Rosas, Luz Angela; Bean, Rachel; Athota, Rani; Czajkowski, Lindsay; Klumpp-Thomas, Carleen; Cervantes-Medina, Adriana; Gouzoulis, Monica; Reed, Susan; Graubard, Barry; Hall, Matthew D; Kalish, Heather; Esposito, Dominic; Kimberly, Robert P; Reis, Steven; Sadtler, Kaitlyn; Memoli, Matthew J.
Afiliação
  • Karkanitsa M; Section on Immunoengineering, National Institute of Biomedical Imaging and Bioengineering (NIBIB), National Institutes of Health (NIH), Bethesda MD 20894.
  • Li Y; Joint Program in Survey Methodology, Department of Epidemiology and Biostatistics, University of Maryland College Park, College Park, MD 20742.
  • Valenti S; Clinical and Translational Science Institute (CTSI), University of Pittsburgh, Pittsburgh, PA 15213.
  • Spathies J; Trans-NIH Shared Resource on Biomedical Engineering and Physical Science (BEPS), NIBIB, NIH, Bethesda MD 20894.
  • Kelly S; Trans-NIH Shared Resource on Biomedical Engineering and Physical Science (BEPS), NIBIB, NIH, Bethesda MD 20894.
  • Hunsberger S; Biostatistics Research Branch, National Institute of Allergy and Infectious Diseases (NIAID), NIH, Bethesda, MD 20894.
  • Yee L; Division of Cancer Treatment and Diagnosis, National Cancer Institute (NCI), NIH, MD 20894.
  • Croker JA; Center for Clinical and Translational Science, University of Alabama at Birmingham, Birmingham, AL, USA.
  • Wang J; Clinical Monitoring Research Program Directorate, Frederick National Laboratory for Cancer Research, Frederick, MD 21702.
  • Alfonso AL; Section on Immunoengineering, National Institute of Biomedical Imaging and Bioengineering (NIBIB), National Institutes of Health (NIH), Bethesda MD 20894.
  • Faust M; Section on Immunoengineering, National Institute of Biomedical Imaging and Bioengineering (NIBIB), National Institutes of Health (NIH), Bethesda MD 20894.
  • Mehalko J; Protein Expression Laboratory, Frederick National Laboratory for Cancer Research, Frederick, MD, 21702.
  • Drew M; Protein Expression Laboratory, Frederick National Laboratory for Cancer Research, Frederick, MD, 21702.
  • Denson JP; Protein Expression Laboratory, Frederick National Laboratory for Cancer Research, Frederick, MD, 21702.
  • Putman Z; Protein Expression Laboratory, Frederick National Laboratory for Cancer Research, Frederick, MD, 21702.
  • Fathi P; Section on Immunoengineering, National Institute of Biomedical Imaging and Bioengineering (NIBIB), National Institutes of Health (NIH), Bethesda MD 20894.
  • Ngo TB; Section on Immunoengineering, National Institute of Biomedical Imaging and Bioengineering (NIBIB), National Institutes of Health (NIH), Bethesda MD 20894.
  • Siripong N; Clinical and Translational Science Institute (CTSI), University of Pittsburgh, Pittsburgh, PA 15213.
  • Baus HA; Laboratory of Immunoregulation, NIAID, NIH, Bethesda MD 20894.
  • Petersen B; Clinical and Translational Science Institute (CTSI), University of Pittsburgh, Pittsburgh, PA 15213.
  • Ford EW; Department of Health Care Organization, and Policy, School of Public Health, University of Alabama at Birmingham, Birmingham, AL, USA.
  • Sundaresan V; Section on Immunoengineering, National Institute of Biomedical Imaging and Bioengineering (NIBIB), National Institutes of Health (NIH), Bethesda MD 20894.
  • Josyula A; Section on Immunoengineering, National Institute of Biomedical Imaging and Bioengineering (NIBIB), National Institutes of Health (NIH), Bethesda MD 20894.
  • Han A; LID Clinical Studies Unit, Laboratory of Infectious Diseases, NIAID, NIH, Bethesda, MD 20894.
  • Giurgea LT; LID Clinical Studies Unit, Laboratory of Infectious Diseases, NIAID, NIH, Bethesda, MD 20894.
  • Rosas LA; LID Clinical Studies Unit, Laboratory of Infectious Diseases, NIAID, NIH, Bethesda, MD 20894.
  • Bean R; LID Clinical Studies Unit, Laboratory of Infectious Diseases, NIAID, NIH, Bethesda, MD 20894.
  • Athota R; LID Clinical Studies Unit, Laboratory of Infectious Diseases, NIAID, NIH, Bethesda, MD 20894.
  • Czajkowski L; LID Clinical Studies Unit, Laboratory of Infectious Diseases, NIAID, NIH, Bethesda, MD 20894.
  • Klumpp-Thomas C; National Center for Advancing Translational Sciences (NCATS), NIH, Rockville, MD 20850.
  • Cervantes-Medina A; LID Clinical Studies Unit, Laboratory of Infectious Diseases, NIAID, NIH, Bethesda, MD 20894.
  • Gouzoulis M; LID Clinical Studies Unit, Laboratory of Infectious Diseases, NIAID, NIH, Bethesda, MD 20894.
  • Reed S; LID Clinical Studies Unit, Laboratory of Infectious Diseases, NIAID, NIH, Bethesda, MD 20894.
  • Graubard B; Division of Cancer Epidemiology & Genetics, Biostatistics Branch, NCI, NIH, Bethesda, MD 20894.
  • Hall MD; National Center for Advancing Translational Sciences (NCATS), NIH, Rockville, MD 20850.
  • Kalish H; Trans-NIH Shared Resource on Biomedical Engineering and Physical Science (BEPS), NIBIB, NIH, Bethesda MD 20894.
  • Esposito D; Protein Expression Laboratory, Frederick National Laboratory for Cancer Research, Frederick, MD, 21702.
  • Kimberly RP; Center for Clinical and Translational Science, University of Alabama at Birmingham, Birmingham, AL, USA.
  • Reis S; Clinical and Translational Science Institute (CTSI), University of Pittsburgh, Pittsburgh, PA 15213.
  • Sadtler K; Section on Immunoengineering, National Institute of Biomedical Imaging and Bioengineering (NIBIB), National Institutes of Health (NIH), Bethesda MD 20894.
  • Memoli MJ; LID Clinical Studies Unit, Laboratory of Infectious Diseases, NIAID, NIH, Bethesda, MD 20894.
medRxiv ; 2023 Oct 21.
Article em En | MEDLINE | ID: mdl-37904956
Due to a combination of asymptomatic or undiagnosed infections, the proportion of the United States population infected with SARS-CoV-2 was unclear from the beginning of the pandemic. We previously established a platform to screen for SARS-CoV-2 positivity across a representative proportion of the US population, from which we reported that almost 17 million Americans were estimated to have had undocumented infections in the Spring of 2020. Since then, vaccine rollout and prevalence of different SARS-CoV-2 variants have further altered seropositivity trends within the United States population. To explore the longitudinal impacts of the pandemic and vaccine responses on seropositivity, we re-enrolled participants from our baseline study in a 6- and 12- month follow-up study to develop a longitudinal antibody profile capable of representing seropositivity within the United States during a critical period just prior to and during the initiation of vaccine rollout. Initial measurements showed that, since July 2020, seropositivity elevated within this population from 4.8% at baseline to 36.2% and 89.3% at 6 and 12 months, respectively. We also evaluated nucleocapsid seropositivity and compared to spike seropositivity to identify trends in infection versus vaccination relative to baseline. These data serve as a window into a critical timeframe within the COVID-19 pandemic response and serve as a resource that could be used in subsequent respiratory illness outbreaks.

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: MedRxiv Ano de publicação: 2023 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: MedRxiv Ano de publicação: 2023 Tipo de documento: Article