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mRNA or ChAd0x1 COVID-19 Vaccination of Adolescents Induces Robust Antibody and Cellular Responses With Continued Recognition of Omicron Following mRNA-1273.
Dowell, Alexander C; Powell, Annabel A; Davis, Chris; Scott, Sam; Logan, Nicola; Willett, Brian J; Bruton, Rachel; Ayodele, Morenike; Jinks, Elizabeth; Gunn, Juliet; Spalkova, Eliska; Sylla, Panagiota; Nicol, Samantha M; Zuo, Jianmin; Ireland, Georgina; Okike, Ifeanyichukwu; Baawuah, Frances; Beckmann, Joanne; Ahmad, Shazaad; Garstang, Joanna; Brent, Andrew J; Brent, Bernadette; White, Marie; Collins, Aedin; Davis, Francesca; Lim, Ming; Cohen, Jonathan; Kenny, Julia; Linley, Ezra; Poh, John; Amirthalingam, Gayatri; Brown, Kevin; Ramsay, Mary E; Azad, Rafaq; Wright, John; Waiblinger, Dagmar; Moss, Paul; Ladhani, Shamez N.
  • Dowell AC; Institute of Immunology & Immunotherapy, College of Medical and Dental Sciences, University of Birmingham, Birmingham, United Kingdom.
  • Powell AA; Immunisation and Vaccine Preventable Diseases Division, United Kingdom (UK) Health Security Agency, London, United Kingdom.
  • Davis C; Medical Research Council (MRC)-University of Glasgow Centre for Virus Research, Glasgow, United Kingdom.
  • Scott S; Medical Research Council (MRC)-University of Glasgow Centre for Virus Research, Glasgow, United Kingdom.
  • Logan N; Medical Research Council (MRC)-University of Glasgow Centre for Virus Research, Glasgow, United Kingdom.
  • Willett BJ; Medical Research Council (MRC)-University of Glasgow Centre for Virus Research, Glasgow, United Kingdom.
  • Bruton R; Institute of Immunology & Immunotherapy, College of Medical and Dental Sciences, University of Birmingham, Birmingham, United Kingdom.
  • Ayodele M; Institute of Immunology & Immunotherapy, College of Medical and Dental Sciences, University of Birmingham, Birmingham, United Kingdom.
  • Jinks E; Institute of Immunology & Immunotherapy, College of Medical and Dental Sciences, University of Birmingham, Birmingham, United Kingdom.
  • Gunn J; Institute of Immunology & Immunotherapy, College of Medical and Dental Sciences, University of Birmingham, Birmingham, United Kingdom.
  • Spalkova E; Institute of Immunology & Immunotherapy, College of Medical and Dental Sciences, University of Birmingham, Birmingham, United Kingdom.
  • Sylla P; Institute of Immunology & Immunotherapy, College of Medical and Dental Sciences, University of Birmingham, Birmingham, United Kingdom.
  • Nicol SM; Institute of Immunology & Immunotherapy, College of Medical and Dental Sciences, University of Birmingham, Birmingham, United Kingdom.
  • Zuo J; Institute of Immunology & Immunotherapy, College of Medical and Dental Sciences, University of Birmingham, Birmingham, United Kingdom.
  • Ireland G; Immunisation and Vaccine Preventable Diseases Division, United Kingdom (UK) Health Security Agency, London, United Kingdom.
  • Okike I; Immunisation and Vaccine Preventable Diseases Division, United Kingdom (UK) Health Security Agency, London, United Kingdom.
  • Baawuah F; University Hospitals of Derby and Burton National Health Service (NHS) Foundation Trust, Derby, United Kingdom.
  • Beckmann J; Immunisation and Vaccine Preventable Diseases Division, United Kingdom (UK) Health Security Agency, London, United Kingdom.
  • Ahmad S; East London National Health Service (NHS) Foundation Trust, London, United Kingdom.
  • Garstang J; Manchester University National Health Service (NHS) Foundation Trust, Manchester, United Kingdom.
  • Brent AJ; Birmingham Community Healthcare National Health Service (NHS) Trust, Aston, United Kingdom.
  • Brent B; Nuffield Department of Medicine, Oxford University Hospitals National Health Service (NHS) Foundation Trust, Oxford, United Kingdom.
  • White M; University of Oxford, Oxford, United Kingdom.
  • Collins A; Nuffield Department of Medicine, Oxford University Hospitals National Health Service (NHS) Foundation Trust, Oxford, United Kingdom.
  • Davis F; Department of General Paediatrics, Evelina London Children's Hospital, London, United Kingdom.
  • Lim M; The National Children's Hospital, Tallaght University Hospital, Dublin, Ireland.
  • Cohen J; Department of General Paediatrics, Evelina London Children's Hospital, London, United Kingdom.
  • Kenny J; Children's Neurosciences, Evelina London Children's Hospital at Guy's and St Thomas' National Health Service (NHS) Foundation Trust, King's Health Partners Academic Health Science Centre, London, United Kingdom.
  • Linley E; Department Women and Children's Health, School of Life Course Sciences (SoLCS), King's College London, London, United Kingdom.
  • Poh J; Department of Paediatric Infectious Diseases and Immunology Evelina London Children's Hospital, London, United Kingdom.
  • Amirthalingam G; Department Women and Children's Health, School of Life Course Sciences (SoLCS), King's College London, London, United Kingdom.
  • Brown K; Department of Paediatric Infectious Diseases and Immunology Evelina London Children's Hospital, London, United Kingdom.
  • Ramsay ME; United Kingdom (UK) Health Security Agency, Manchester Royal Infirmary, Manchester, United Kingdom.
  • Azad R; Immunisation and Vaccine Preventable Diseases Division, United Kingdom (UK) Health Security Agency, London, United Kingdom.
  • Wright J; Immunisation and Vaccine Preventable Diseases Division, United Kingdom (UK) Health Security Agency, London, United Kingdom.
  • Waiblinger D; Immunisation and Vaccine Preventable Diseases Division, United Kingdom (UK) Health Security Agency, London, United Kingdom.
  • Moss P; Immunisation and Vaccine Preventable Diseases Division, United Kingdom (UK) Health Security Agency, London, United Kingdom.
  • Ladhani SN; Bradford Institute for Health Research, Bradford Teaching Hospitals National Health Service (NHS) Foundation Trust, Bradford, United Kingdom.
Front Immunol ; 13: 882515, 2022.
Article in English | MEDLINE | ID: covidwho-1903016
ABSTRACT
Children and adolescents generally experience mild COVID-19. However, those with underlying physical health conditions are at a significantly increased risk of severe disease. Here, we present a comprehensive analysis of antibody and cellular responses in adolescents with severe neuro-disabilities who received COVID-19 vaccination with either ChAdOx1 (n=6) or an mRNA vaccine (mRNA-1273, n=8, BNT162b2, n=1). Strong immune responses were observed after vaccination and antibody levels and neutralisation titres were both higher after two doses. Both measures were also higher after mRNA vaccination and were further enhanced by prior natural infection where one vaccine dose was sufficient to generate peak antibody response. Robust T-cell responses were generated after dual vaccination and were also higher following mRNA vaccination. Early T-cells were characterised by a dominant effector-memory CD4+ T-cell population with a type-1 cytokine signature with additional production of IL-10. Antibody levels were well-maintained for at least 3 months after vaccination and 3 of 4 donors showed measurable neutralisation titres against the Omicron variant. T-cell responses also remained robust, with generation of a central/stem cell memory pool and showed strong reactivity against Omicron spike. These data demonstrate that COVID-19 vaccines display strong immunogenicity in adolescents and that dual vaccination, or single vaccination following prior infection, generate higher immune responses than seen after natural infection and develop activity against Omicron. Initial evidence suggests that mRNA vaccination elicits stronger immune responses than adenoviral delivery, although the latter is also higher than seen in adult populations. COVID-19 vaccines are therefore highly immunogenic in high-risk adolescents and dual vaccination might be able to provide relative protection against the Omicron variant that is currently globally dominant.
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Full text: Available Collection: International databases Database: MEDLINE Main subject: COVID-19 Vaccines / COVID-19 Type of study: Prognostic study Topics: Vaccines / Variants Limits: Adolescent / Adult / Child / Humans Language: English Journal: Front Immunol Year: 2022 Document Type: Article Affiliation country: Fimmu.2022.882515

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Full text: Available Collection: International databases Database: MEDLINE Main subject: COVID-19 Vaccines / COVID-19 Type of study: Prognostic study Topics: Vaccines / Variants Limits: Adolescent / Adult / Child / Humans Language: English Journal: Front Immunol Year: 2022 Document Type: Article Affiliation country: Fimmu.2022.882515