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Differential antibody production by symptomatology in SARS-CoV-2 convalescent individuals
Sharada Saraf; Xianming Zhu; Ruchee Shrestha; Tania S. Bonny; Owen R. Baker; Evan J. Beck; Reinaldo E. Fernandez; Yolanda Eby; Olivia Akinde; Jessica E. Ruff; Patrizio Caturegli; Andrew D. Redd; Evan M. Bloch; Thomas C. Quinn; Aaron AR Tobian; Oliver Laeyendecker.
Afiliação
  • Sharada Saraf; NIAID DIR: National Institute of Allergy and Infectious Diseases Division of Intramural Research
  • Xianming Zhu; Johns Hopkins University - Homewood Campus: Johns Hopkins University
  • Ruchee Shrestha; Johns Hopkins University
  • Tania S. Bonny; Johns Hopkins University
  • Owen R. Baker; Johns Hopkins University
  • Evan J. Beck; NIAID DIR: National Institute of Allergy and Infectious Diseases Division of Intramural Research
  • Reinaldo E. Fernandez; Johns Hopkins University
  • Yolanda Eby; Johns Hopkins University
  • Olivia Akinde; Johns Hopkins University
  • Jessica E. Ruff; Johns Hopkins University
  • Patrizio Caturegli; Johns Hopkins University
  • Andrew D. Redd; NIAID DIR: National Institute of Allergy and Infectious Diseases Division of Intramural Research
  • Evan M. Bloch; Johns Hopkins University
  • Thomas C. Quinn; NIAID DIR: National Institute of Allergy and Infectious Diseases Division of Intramural Research
  • Aaron AR Tobian; Johns Hopkins University
  • Oliver Laeyendecker; NIAID
Preprint em En | PREPRINT-MEDRXIV | ID: ppmedrxiv-22270718
ABSTRACT
The association between COVID-19 symptoms and antibody responses against SARS-CoV-2 is poorly characterized. We analyzed antibody levels in individuals with known SARS-CoV-2 infection to identify potential antibody-symptom associations. Convalescent plasma from 216 SARS-CoV-2 RNA+ individuals with symptomatology information were tested for the presence of IgG to the spike S1 subunit (Euroimmun ELISA), IgG to receptor binding domain (RBD, CoronaCHEK rapid test), and for IgG, IgA, and IgM to nucleocapsid (N, Bio-Rad ELISA). Logistic regression was used to estimate the odds of having a COVID-19 symptom from the antibody response, adjusting for sex and age. Cough strongly associated with antibodies against S1 (adjusted odds ratio [aOR]= 5.33; 95% CI from 1.51 to 18.86) and RBD (aOR=4.36; CI 1.49, 12.78). In contrast, sore throat significantly associated with the absence of antibodies to S1 and N (aOR=0.25; CI 0.08, 0.80 and aOR=0.31; 0.11, 0.91). Similarly, lack of symptoms associated with the absence of antibodies to N and RBD (aOR=0.16; CI 0.03, 0.97 and aOR=0.16; CI 0.03, 1.01). Cough appeared to be correlated with a seropositive result, suggesting that SARS-CoV-2 infected individuals exhibiting lower respiratory symptoms generate a robust antibody response. Conversely, those without symptoms or limited to a sore throat while infected with SARS-CoV-2 were likely to lack a detectable antibody response. These findings strongly support the notion that severity of infection correlates with robust antibody response.
Licença
cc0
Texto completo: 1 Coleções: 09-preprints Base de dados: PREPRINT-MEDRXIV Tipo de estudo: Prognostic_studies Idioma: En Ano de publicação: 2022 Tipo de documento: Preprint
Texto completo: 1 Coleções: 09-preprints Base de dados: PREPRINT-MEDRXIV Tipo de estudo: Prognostic_studies Idioma: En Ano de publicação: 2022 Tipo de documento: Preprint
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