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Serum HCoV-spike specific antibodies do not protect against subsequent SARS-CoV-2 infection in children and adolescents.
Ratcliffe, Helen; Tiley, Karen S; Longet, Stephanie; Tonry, Claire; Roarty, Cathal; Watson, Chris; Amirthalingam, Gayatri; Vichos, Iason; Morey, Ella; Douglas, Naomi L; Marinou, Spyridoula; Plested, Emma; Aley, Parvinder K; Galiza, Eva; Faust, Saul N; Hughes, Stephen; Murray, Clare; Roderick, Marion R; Shackley, Fiona; Oddie, Sam; Lee, Tim W R; Turner, David P J; Raman, Mala; Owens, Stephen; Turner, Paul J; Cockerill, Helen; Lopez Bernal, Jamie; Ijaz, Samreen; Poh, John; Shute, Justin; Linley, Ezra; Borrow, Ray; Hoschler, Katja; Brown, Kevin E; Carroll, Miles W; Klenerman, Paul; Dunachie, Susanna J; Ramsay, Mary; Voysey, Merryn; Waterfield, Thomas; Snape, Matthew D.
Affiliation
  • Ratcliffe H; Centre for Clinical Vaccinology and Tropical Medicine, University of Oxford, Oxford, UK.
  • Tiley KS; Centre for Clinical Vaccinology and Tropical Medicine, University of Oxford, Oxford, UK.
  • Longet S; Wellcome Centre for Human Genetics, Nuffield Department of Medicine, University of Oxford, Oxford, UK.
  • Tonry C; Wellcome-Wolfson Institute for Experimental Medicine, Queen's University Belfast- School of Medicine, Dentistry and Biomedical Sciences, Belfast, UK.
  • Roarty C; Wellcome-Wolfson Institute for Experimental Medicine, Queen's University Belfast- School of Medicine, Dentistry and Biomedical Sciences, Belfast, UK.
  • Watson C; Wellcome-Wolfson Institute for Experimental Medicine, Queen's University Belfast- School of Medicine, Dentistry and Biomedical Sciences, Belfast, UK.
  • Amirthalingam G; UK Health Security Agency.
  • Vichos I; Centre for Clinical Vaccinology and Tropical Medicine, University of Oxford, Oxford, UK.
  • Morey E; Centre for Clinical Vaccinology and Tropical Medicine, University of Oxford, Oxford, UK.
  • Douglas NL; Centre for Clinical Vaccinology and Tropical Medicine, University of Oxford, Oxford, UK.
  • Marinou S; Centre for Clinical Vaccinology and Tropical Medicine, University of Oxford, Oxford, UK.
  • Plested E; Centre for Clinical Vaccinology and Tropical Medicine, University of Oxford, Oxford, UK.
  • Aley PK; Centre for Clinical Vaccinology and Tropical Medicine, University of Oxford, Oxford, UK.
  • Galiza E; St Georges Hospital NHS Foundation Trust.
  • Faust SN; NIHR Southampton Clinical Research Facility, University Hospital Southampton NHS Foundation Trust and Faculty of Medicine and Institute of Life Sciences, University of Southampton.
  • Hughes S; National Immunisation Schedule Evaluation Consortium.
  • Murray C; Manchester University NHS Foundation Trust, NIHR Manchester Biomedical Research Centre, Manchester Academic Health Science Centre, Manchester, UK.
  • Roderick MR; Manchester University NHS Foundation Trust, NIHR Manchester Biomedical Research Centre, Manchester Academic Health Science Centre, Manchester, UK.
  • Shackley F; Division of Infection, Immunity and Respiratory Medicine, School of Biological Sciences, University of Manchester, Manchester, UK.
  • Oddie S; University Hospitals Bristol NHS Foundation Trust.
  • Lee TWR; Sheffield Children's Hospital NHS Trust.
  • Turner DPJ; Bradford Teaching Hospitals NHS Foundation Trust.
  • Raman M; Leeds Teaching Hospitals NHS Trust.
  • Owens S; School of Life Sciences, University of Nottingham.
  • Turner PJ; Nottingham University Hospitals NHS Trust.
  • Cockerill H; University Hospitals Plymouth NHS Trust.
  • Lopez Bernal J; The Newcastle Upon Tyne Hospitals NHS Foundation Trust.
  • Ijaz S; National Heart & Lung Institute, Imperial College London.
  • Poh J; National Heart & Lung Institute, Imperial College London.
  • Shute J; UK Health Security Agency.
  • Linley E; UK Health Security Agency.
  • Borrow R; UK Health Security Agency.
  • Hoschler K; UK Health Security Agency.
  • Brown KE; UK Health Security Agency.
  • Carroll MW; UK Health Security Agency.
  • Klenerman P; UK Health Security Agency.
  • Dunachie SJ; UK Health Security Agency.
  • Ramsay M; Wellcome Centre for Human Genetics, Nuffield Department of Medicine, University of Oxford, Oxford, UK.
  • Voysey M; Translational Gastroenterology Unit, University of Oxford, Oxford, UK.
  • Waterfield T; National Institute for Health Research (NIHR) Oxford BRC.
  • Snape MD; National Institute for Health Research (NIHR) Oxford BRC.
iScience ; 26(12): 108500, 2023 Dec 15.
Article in En | MEDLINE | ID: mdl-38089581
ABSTRACT
SARS-CoV-2 infections in children are generally asymptomatic or mild and rarely progress to severe disease and hospitalization. Why this is so remains unclear. Here we explore the potential for protection due to pre-existing cross-reactive seasonal coronavirus antibodies and compare the rate of antibody decline for nucleocapsid and spike protein in serum and oral fluid against SARS-CoV-2 within the pediatric population. No differences in seasonal coronaviruses antibody concentrations were found at baseline between cases and controls, suggesting no protective effect from pre-existing immunity against seasonal coronaviruses. Antibodies against seasonal betacoronaviruses were boosted in response to SARS-CoV-2 infection. In serum, anti-nucleocapsid antibodies fell below the threshold of positivity more quickly than anti-spike protein antibodies. These findings add to our understanding of protection against infection with SARS-CoV-2 within the pediatric population, which is important when considering pediatric SARS-CoV-2 immunization policies.
Key words

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: IScience Year: 2023 Document type: Article

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: IScience Year: 2023 Document type: Article