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SARS-CoV-2 Humoral Immune Responses in Convalescent Individuals Over 12 Months Reveal Severity-Dependent Antibody Dynamics.
Siles, Nadia; Schuler, Maisey; Maguire, Cole; Amengor, Dzifa; Nguyen, Annalee; Wilen, Rebecca; Rogers, Jacob; Bazzi, Sam; Caslin, Blaine; DiPasquale, Christopher; Abigania, Melissa; Olson, Eric; Creaturo, Janelle; Hurley, Kerin; Triplett, Todd A; Rousseau, Justin F; Strakowski, Stephen M; Wylie, Dennis; Maynard, Jennifer; Ehrlich, Lauren I R; Melamed, Esther.
Afiliação
  • Siles N; Department of Neurology, Dell Medical School, University of Texas at Austin, Austin, Texas.
  • Schuler M; Department of Neurology, Dell Medical School, University of Texas at Austin, Austin, Texas.
  • Maguire C; Department of Neurology, Dell Medical School, University of Texas at Austin, Austin, Texas.
  • Amengor D; Department of Molecular Biosciences, University of Texas at Austin, Austin, Texas.
  • Nguyen A; Department of Chemical Engineering, University of Texas at Austin, Austin, Texas.
  • Wilen R; Department of Chemical Engineering, University of Texas at Austin, Austin, Texas.
  • Rogers J; Department of Neurology, Dell Medical School, University of Texas at Austin, Austin, Texas.
  • Bazzi S; Department of Neurology, Dell Medical School, University of Texas at Austin, Austin, Texas.
  • Caslin B; Department of Neurology, Dell Medical School, University of Texas at Austin, Austin, Texas.
  • DiPasquale C; Babson Diagnostics, Austin, Texas.
  • Abigania M; Babson Diagnostics, Austin, Texas.
  • Olson E; Babson Diagnostics, Austin, Texas.
  • Creaturo J; Department of Neurology, Dell Medical School, University of Texas at Austin, Austin, Texas.
  • Hurley K; Department of Neurology, Dell Medical School, University of Texas at Austin, Austin, Texas; Dell Seton Medical Center at the University of Texas, Austin, Texas.
  • Triplett TA; Department of Oncology Dell Medical School, University of Texas at Austin, Austin, Texas; Department of Immunotherapeutics & Biotechnology, School of Pharmacy, Texas Tech University Health Sciences Center, Abilene, TX, USA.
  • Rousseau JF; Department of Neurology, Dell Medical School, University of Texas at Austin, Austin, Texas; Department of Population Health, Dell Medical School, University of Texas at Austin, Austin, Texas.
  • Strakowski SM; Department of Psychiatry, Indiana University School of Medicine, Indianapolis; Department of Psychiatry, Dell Medical School, University of Texas at Austin, Austin, Texas.
  • Wylie D; Center for Biomedical Research Support, University of Texas at Austin, Austin Texas.
  • Maynard J; Department of Chemical Engineering, University of Texas at Austin, Austin, Texas.
  • Ehrlich LIR; Department of Molecular Biosciences, University of Texas at Austin, Austin, Texas.
  • Melamed E; Department of Neurology, Dell Medical School, University of Texas at Austin, Austin, Texas.
medRxiv ; 2023 Dec 07.
Article em En | MEDLINE | ID: mdl-38106077
ABSTRACT

Background:

Understanding the kinetics and longevity of antibody responses to SARS-CoV-2 is critical to informing strategies toward reducing Coronavirus disease 2019 (COVID-19) reinfections, and improving vaccination and therapy approaches.

Methods:

We evaluated antibody titers against SARS-CoV-2 nucleocapsid (N), spike (S), and receptor binding domain (RBD) of spike in 98 convalescent participants who experienced asymptomatic, mild, moderate or severe COVID-19 disease and in 17 non-vaccinated, non-infected controls, using four different antibody assays. Participants were sampled longitudinally at 1, 3, 6, and 12 months post-SARS-CoV-2 positive PCR test.

Findings:

Increasing acute COVID-19 disease severity correlated with higher anti-N and anti-RBD antibody titers throughout 12 months post-infection. Anti-N and anti-RBD titers declined over time in all participants, with the exception of increased anti-RBD titers post-vaccination, and the decay rates were faster in hospitalized compared to non-hospitalized participants. <50% of participants retained anti-N titers above control levels at 12 months, with non-hospitalized participants falling below control levels sooner. Nearly all hospitalized and non-hospitalized participants maintained anti-RBD titers above controls for up to 12 months, suggesting longevity of protection against severe reinfections. Nonetheless, by 6 months, few participants retained >50% of their 1-month anti-N or anti-RBD titers. Vaccine-induced increases in anti-RBD titers were greater in non-hospitalized relative to hospitalized participants. Early convalescent antibody titers correlated with age, but no association was observed between Post-Acute Sequelae of SARS-CoV-2 infection (PASC) status or acute steroid treatment and convalescent antibody titers.

Interpretation:

Hospitalized participants developed higher anti-SARS-CoV-2 antibody titers relative to non-hospitalized participants, a difference that persisted throughout 12 months, despite the faster decline in titers in hospitalized participants. In both groups, while anti-N titers fell below control levels for at least half of the participants, anti-RBD titers remained above control levels for almost all participants over 12 months, demonstrating generation of long-lived antibody responses known to correlate with protection from severe disease across COVID-19 severities. Overall, our findings contribute to the evolving understanding of COVID-19 antibody dynamics.

Funding:

Austin Public Health, NIAAA, Babson Diagnostics, Dell Medical School Startup.

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