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Relationship between HLA genetic variations, COVID-19 vaccine antibody response, and risk of breakthrough outcomes.
Xie, Junqing; Mothe, Beatriz; Alcalde Herraiz, Marta; Li, Chunxiao; Xu, Yu; Jödicke, Annika M; Gao, Yaqing; Wang, Yunhe; Feng, Shuo; Wei, Jia; Chen, Zhuoyao; Hong, Shenda; Wu, Yeda; Su, Binbin; Zheng, Xiaoying; Cohet, Catherine; Ali, Raghib; Wareham, Nick; Alhambra, Daniel Prieto.
  • Xie J; Centre for Statistics in Medicine and NIHR Biomedical Research Centre Oxford, NDORMS, University of Oxford, Oxford, UK.
  • Mothe B; Infectious Diseases Department, IrsiCaixa AIDS Research Institute, Hospital Universitari Germans Trias i Pujol, Badalona, Spain.
  • Alcalde Herraiz M; Centre for Statistics in Medicine and NIHR Biomedical Research Centre Oxford, NDORMS, University of Oxford, Oxford, UK.
  • Li C; Medical Research Council Epidemiology Unit, University of Cambridge, Cambridge, UK.
  • Xu Y; Cambridge Baker Systems Genomics Initiative, Department of Public Health and Primary Care, University of Cambridge, Cambridge, UK.
  • Jödicke AM; British Heart Foundation Cardiovascular Epidemiology Unit, Department of Public Health and Primary Care, University of Cambridge, Cambridge, UK.
  • Gao Y; Victor Phillip Dahdaleh Heart and Lung Research Institute, University of Cambridge, Cambridge, UK.
  • Wang Y; Centre for Statistics in Medicine and NIHR Biomedical Research Centre Oxford, NDORMS, University of Oxford, Oxford, UK.
  • Feng S; Nuffield Department of Population Health, Big Data Institute, University of Oxford, Oxford, UK.
  • Wei J; Nuffield Department of Population Health, Big Data Institute, University of Oxford, Oxford, UK.
  • Chen Z; Oxford Vaccine Group, Department of Paediatrics, University of Oxford, Oxford, UK.
  • Hong S; Nuffield Department of Medicine, Big Data Institute, University of Oxford, Oxford, UK.
  • Wu Y; Centre for Medicines Discovery, Nuffield Department of Medicine, University of Oxford, Oxford, UK.
  • Su B; National Institute of Health Data Science, Peking University, Beijing, China.
  • Zheng X; Institute of Medical Technology, Peking University Health Science Center, Beijing, China.
  • Cohet C; Institute for Molecular Bioscience, The University of Queensland, Brisbane, QLD, Australia.
  • Ali R; School of Population Medicine and Public Health, Chinese Academy of Medical Sciences/Peking Union Medical College, Beijing, China.
  • Wareham N; School of Population Medicine and Public Health, Chinese Academy of Medical Sciences/Peking Union Medical College, Beijing, China.
  • Alhambra DP; Real-World Evidence Workstream, Data Analytics and Methods Task Force, European Medicines Agency, Amsterdam, Noord-Holland, The Netherlands.
Nat Commun ; 15(1): 4031, 2024 May 13.
Article en En | MEDLINE | ID: mdl-38740772
ABSTRACT
The rapid global distribution of COVID-19 vaccines, with over a billion doses administered, has been unprecedented. However, in comparison to most identified clinical determinants, the implications of individual genetic factors on antibody responses post-COVID-19 vaccination for breakthrough outcomes remain elusive. Here, we conducted a population-based study including 357,806 vaccinated participants with high-resolution HLA genotyping data, and a subset of 175,000 with antibody serology test results. We confirmed prior findings that single nucleotide polymorphisms associated with antibody response are predominantly located in the Major Histocompatibility Complex region, with the expansive HLA-DQB1*06 gene alleles linked to improved antibody responses. However, our results did not support the claim that this mutation alone can significantly reduce COVID-19 risk in the general population. In addition, we discovered and validated six HLA alleles (A*0301, C*1601, DQA1*0102, DQA1*0101, DRB3*0101, and DPB1*1001) that independently influence antibody responses and demonstrated a combined effect across HLA genes on the risk of breakthrough COVID-19 outcomes. Lastly, we estimated that COVID-19 vaccine-induced antibody positivity provides approximately 20% protection against infection and 50% protection against severity. These findings have immediate implications for functional studies on HLA molecules and can inform future personalised vaccination strategies.
Asunto(s)

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Polimorfismo de Nucleótido Simple / Alelos / Vacunas contra la COVID-19 / SARS-CoV-2 / COVID-19 / Antígenos HLA / Anticuerpos Antivirales Límite: Adult / Female / Humans / Male / Middle aged Idioma: En Año: 2024 Tipo del documento: Article

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Polimorfismo de Nucleótido Simple / Alelos / Vacunas contra la COVID-19 / SARS-CoV-2 / COVID-19 / Antígenos HLA / Anticuerpos Antivirales Límite: Adult / Female / Humans / Male / Middle aged Idioma: En Año: 2024 Tipo del documento: Article