Your browser doesn't support javascript.
Antibody Persistence After Primary SARS-CoV-2 Infection and Protection Against Future Variants Including Omicron in Adolescents: National, Prospective Cohort Study.
Aiano, Felicity; Ireland, Georgina; Baawuah, Frances; Beckmann, Joanne; Okike, Ifeanyichukwu O; Ahmad, Shazaad; Garstang, Joanna; Brent, Andrew J; Brent, Bernadette; Borrow, Ray; Linley, Ezra; Ho, Sammy; Carr, Christine; Zambon, Maria; Poh, John; Warrener, Lenesha; Amirthalingam, Gayatri; Brown, Kevin E; Ramsay, Mary E; Hoschler, Katja; Ladhani, Shamez N.
  • Aiano F; From the Immunisation and Vaccine Preventable Diseases Division, UK Health Security Agency.
  • Ireland G; From the Immunisation and Vaccine Preventable Diseases Division, UK Health Security Agency.
  • Baawuah F; From the Immunisation and Vaccine Preventable Diseases Division, UK Health Security Agency.
  • Beckmann J; East London NHS Foundation Trust, London.
  • Okike IO; From the Immunisation and Vaccine Preventable Diseases Division, UK Health Security Agency.
  • Ahmad S; University Hospitals of Derby and Burton NHS Foundation Trust, Derby.
  • Garstang J; Manchester University NHS Foundation Trust, Manchester.
  • Brent AJ; Birmingham Community Healthcare NHS Trust, Aston.
  • Brent B; Nuffield Department of Medicine, Oxford University Hospitals NHS Foundation Trust.
  • Borrow R; University of Oxford, Oxford.
  • Linley E; Nuffield Department of Medicine, Oxford University Hospitals NHS Foundation Trust.
  • Ho S; UK Health Security Agency, Manchester Royal Infirmary, Manchester.
  • Carr C; UK Health Security Agency, Manchester Royal Infirmary, Manchester.
  • Zambon M; From the Immunisation and Vaccine Preventable Diseases Division, UK Health Security Agency.
  • Poh J; From the Immunisation and Vaccine Preventable Diseases Division, UK Health Security Agency.
  • Warrener L; From the Immunisation and Vaccine Preventable Diseases Division, UK Health Security Agency.
  • Amirthalingam G; From the Immunisation and Vaccine Preventable Diseases Division, UK Health Security Agency.
  • Brown KE; From the Immunisation and Vaccine Preventable Diseases Division, UK Health Security Agency.
  • Ramsay ME; From the Immunisation and Vaccine Preventable Diseases Division, UK Health Security Agency.
  • Hoschler K; From the Immunisation and Vaccine Preventable Diseases Division, UK Health Security Agency.
  • Ladhani SN; From the Immunisation and Vaccine Preventable Diseases Division, UK Health Security Agency.
Pediatr Infect Dis J ; 42(6): 496-502, 2023 06 01.
Article in English | MEDLINE | ID: covidwho-2248375
ABSTRACT

BACKGROUND:

Antibodies are a measure of immunity after primary infection, which may help protect against further SARS-CoV-2 infections. They may also provide some cross-protection against SARS-CoV-2 variants. There are limited data on antibody persistence and, especially, cross-reactivity against different SARS-CoV-2 variants after primary infection in children.

METHODS:

We initiated enhanced surveillance in 18 secondary schools to monitor SARS-CoV-2 infection and transmission in September 2020. Students and Staff provided longitudinal blood samples to test for variant-specific SARS-CoV-2 antibodies using in-house receptor binding domain assays. We recruited 1189 students and 1020 staff; 160 (97 students, 63 staff) were SARS-CoV-2 nucleocapsid-antibody positive at baseline and had sufficient serum for further analysis.

RESULTS:

Most participants developed sustained antibodies against their infecting [wild-type (WT)] strain as well as cross-reactive antibodies against the Alpha, Beta and Delta variants but at lower titers than WT. Staff had significantly lower antibodies titers against WT as cross-reactive antibodies against the Alpha, Beta and Delta variants than students (all P < 0.01). In participants with sufficient sera, only 2.3% (1/43) students and 17.2% (5/29) staff had cross-reactive antibodies against the Omicron variant; they also had higher antibody titers against WT (3042.5; 95% confidence interval 769.0-12,036.2) than those who did not have cross-reactive antibodies against the Omicron variant (680.7; 534.2-867.4).

CONCLUSIONS:

We found very high rates of antibody persistence after primary infection with WT in students and staff. Infection with WT induced cross-reactive antibodies against Alpha, Beta and Delta variants, but not Omicron. Primary infection with WT may not be cross-protective against the Omicron variant.
Subject(s)

Full text: Available Collection: International databases Database: MEDLINE Main subject: SARS-CoV-2 / COVID-19 Type of study: Cohort study / Observational study / Prognostic study / Randomized controlled trials Topics: Variants Limits: Adolescent / Child / Humans Language: English Journal: Pediatr Infect Dis J Journal subject: Communicable Diseases / Pediatrics Year: 2023 Document Type: Article

Similar

MEDLINE

...
LILACS

LIS


Full text: Available Collection: International databases Database: MEDLINE Main subject: SARS-CoV-2 / COVID-19 Type of study: Cohort study / Observational study / Prognostic study / Randomized controlled trials Topics: Variants Limits: Adolescent / Child / Humans Language: English Journal: Pediatr Infect Dis J Journal subject: Communicable Diseases / Pediatrics Year: 2023 Document Type: Article