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Long-term immune response to SARS-CoV-2 infection and vaccination in children and adolescents.
Messiah, Sarah E; Talebi, Yashar; Swartz, Michael D; Sabharwal, Rachit; Han, Haoting; Bergqvist, Emma; Kohl, Harold W; Valerio-Shewmaker, Melissa; DeSantis, Stacia M; Yaseen, Ashraf; Kelder, Steven H; Ross, Jessica; Padilla, Lindsay N; Gonzalez, Michael O; Wu, Leqing; Lakey, David; Shuford, Jennifer A; Pont, Stephen J; Boerwinkle, Eric.
Affiliation
  • Messiah SE; Department of Epidemiology, Human Genetics and Environmental Sciences, The University of Texas Health (UTHealth) Science Center at Houston, School of Public Health in Dallas, Dallas, TX, USA. Sarah.E.Messiah@uth.tmc.edu.
  • Talebi Y; Center for Pediatric Population Health, UTHealth School of Public Health, Dallas, TX, USA. Sarah.E.Messiah@uth.tmc.edu.
  • Swartz MD; Department of Pediatrics, McGovern Medical School, Houston, TX, USA. Sarah.E.Messiah@uth.tmc.edu.
  • Sabharwal R; Department of Biostatistics and Data Science, UTHealth Science Center at Houston, School of Public Health in Houston, Houston, TX, USA.
  • Han H; Department of Biostatistics and Data Science, UTHealth Science Center at Houston, School of Public Health in Houston, Houston, TX, USA.
  • Bergqvist E; Department of Biostatistics and Data Science, UTHealth Science Center at Houston, School of Public Health in Houston, Houston, TX, USA.
  • Kohl HW; Department of Biostatistics and Data Science, UTHealth Science Center at Houston, School of Public Health in Houston, Houston, TX, USA.
  • Valerio-Shewmaker M; Department of Epidemiology, Human Genetics and Environmental Sciences, The University of Texas Health (UTHealth) Science Center at Houston, School of Public Health in Dallas, Dallas, TX, USA.
  • DeSantis SM; Center for Pediatric Population Health, UTHealth School of Public Health, Dallas, TX, USA.
  • Yaseen A; Department of Epidemiology, Human Genetics and Environmental Sciences, UTHealth Science Center at Houston, School of Public Health in Austin, Austin, TX, USA.
  • Kelder SH; Department of Kinesiology and Health Education, University of Texas at Austin, Austin, TX, USA.
  • Ross J; Department of Health Promotion and Behavioral Sciences, The University of Texas Health Science Center at Houston, School of Public Health in Brownville, Brownsville, TX, USA.
  • Padilla LN; Department of Biostatistics and Data Science, UTHealth Science Center at Houston, School of Public Health in Houston, Houston, TX, USA.
  • Gonzalez MO; Department of Biostatistics and Data Science, UTHealth Science Center at Houston, School of Public Health in Houston, Houston, TX, USA.
  • Wu L; Department of Epidemiology, Human Genetics and Environmental Sciences, UTHealth Science Center at Houston, School of Public Health in Austin, Austin, TX, USA.
  • Lakey D; Department of Epidemiology, Human Genetics and Environmental Sciences, The University of Texas Health (UTHealth) Science Center at Houston, School of Public Health in Dallas, Dallas, TX, USA.
  • Shuford JA; Department of Epidemiology, Human Genetics and Environmental Sciences, The University of Texas Health Science Center at Houston, School of Public Health, Houston, TX, USA.
  • Pont SJ; Department of Epidemiology, Human Genetics and Environmental Sciences, The University of Texas Health (UTHealth) Science Center at Houston, School of Public Health in Dallas, Dallas, TX, USA.
  • Boerwinkle E; Department of Epidemiology, Human Genetics and Environmental Sciences, The University of Texas Health Science Center at Houston, School of Public Health, Houston, TX, USA.
Pediatr Res ; 2023 Oct 24.
Article in En | MEDLINE | ID: mdl-37875728
ABSTRACT

BACKGROUND:

This analysis examined the durability of antibodies present after SARS-CoV-2 infection and vaccination in children and adolescents.

METHODS:

Data were collected over 4 time points between October 2020-November 2022 as part of a prospective population-based cohort aged 5-to-19 years (N = 810). Results of the (1) Roche Elecsys® Anti-SARS-CoV-2 Immunoassay for detection of antibodies to the SARS-CoV-2 nucleocapsid protein (Roche N-test); and (2) qualitative and semi-quantitative detection of antibodies to the SARS CoV-2 spike protein receptor binding domain (Roche S-test); and (3) self-reported antigen/PCR COVID-19 test results, vaccination and symptom status were analyzed.

RESULTS:

N antibody levels reached a median of 84.10 U/ml (IQR 20.2, 157.7) cutoff index (COI) ~ 6 months post-infection and increased slightly to a median of 85.25 (IQR 28.0, 143.0) COI at 12 months post-infection. Peak S antibody levels were reached at a median of 2500 U/mL ~6 months post-vaccination and remained for ~12 months (mean 11.6 months, SD 1.20).

CONCLUSIONS:

This analysis provides evidence of robust durability of nucleocapsid and spike antibodies in a large pediatric sample up to 12 months post-infection/vaccination. This information can inform pediatric SARS-CoV-2 vaccination schedules. IMPACT This study provided evidence of robust durability of both nucleocapsid and spike antibodies in a large pediatric sample up to 12 months after infection. Little is known about the long-term durability of natural and vaccine-induced SARS-CoV-2 antibodies in the pediatric population. Here, we determined the durability of anti-SARS-CoV-2 spike (S-test) and nucleocapsid protein (N-test) in children/adolescents after SARS-CoV-2 infection and/or vaccination lasts at least up to 12 months. This information can inform future SARS-CoV-2 vaccination schedules in this age group.

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: Pediatr Res Year: 2023 Document type: Article Affiliation country: Estados Unidos

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: Pediatr Res Year: 2023 Document type: Article Affiliation country: Estados Unidos