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ELF5 is a potential respiratory epithelial cell-specific risk gene for severe COVID-19.
Pietzner, Maik; Chua, Robert Lorenz; Wheeler, Eleanor; Jechow, Katharina; Willett, Julian D S; Radbruch, Helena; Trump, Saskia; Heidecker, Bettina; Zeberg, Hugo; Heppner, Frank L; Eils, Roland; Mall, Marcus A; Richards, J Brent; Sander, Leif-Erik; Lehmann, Irina; Lukassen, Sören; Wareham, Nicholas J; Conrad, Christian; Langenberg, Claudia.
Afiliação
  • Pietzner M; Computational Medicine, Berlin Institute of Health (BIH) at Charité - Universitätsmedizin Berlin, Berlin, Germany. maik.pietzner@bih-charite.de.
  • Chua RL; MRC Epidemiology Unit, University of Cambridge, Cambridge, UK. maik.pietzner@bih-charite.de.
  • Wheeler E; Center for Digital Health, Berlin Institute of Health (BIH) at Charité - Universitätsmedizin Berlin, Berlin, Germany.
  • Jechow K; MRC Epidemiology Unit, University of Cambridge, Cambridge, UK.
  • Willett JDS; Center for Digital Health, Berlin Institute of Health (BIH) at Charité - Universitätsmedizin Berlin, Berlin, Germany.
  • Radbruch H; McGill Genome Centre, McGill University, Montréal, QC, Canada.
  • Trump S; Lady Davis Institute, Jewish General Hospital, Montréal, QC, Canada.
  • Heidecker B; Department of Neuropathology, Charité - Universitätsmedizin Berlin, corporate member of Freie Universität Berlin und Humboldt-Universität zu Berlin, Berlin, Germany.
  • Zeberg H; Molecular Epidemiology Unit, Center for Digital Health, Berlin Institute of Health (BIH) at Charité - Universitätsmedizin Berlin, Berlin, Germany.
  • Heppner FL; Department of Cardiology, Charité - Universitätsmedizin Berlin, corporate member of Freie Universität Berlin und Humboldt-Universität zu Berlin, Berlin, Germany.
  • Eils R; Max Planck Institute for Evolutionary Anthropology, Leipzig, Germany.
  • Mall MA; Department of Neuroscience, Karolinska Institutet, Stockholm, Sweden.
  • Richards JB; Department of Neuropathology, Charité - Universitätsmedizin Berlin, corporate member of Freie Universität Berlin und Humboldt-Universität zu Berlin, Berlin, Germany.
  • Sander LE; Cluster of Excellence, NeuroCure, Berlin, Germany.
  • Lehmann I; German Center for Neurodegenerative Diseases (DZNE) Berlin, Berlin, Germany.
  • Lukassen S; Center for Digital Health, Berlin Institute of Health (BIH) at Charité - Universitätsmedizin Berlin, Berlin, Germany.
  • Wareham NJ; Health Data Science Unit, Heidelberg University Hospital and BioQuant, Heidelberg, Germany.
  • Conrad C; German Center for Lung Research (DZL), associated partner site, Augustenburger Platz 1, 13353, Berlin, Germany.
  • Langenberg C; German Center for Lung Research (DZL), associated partner site, Augustenburger Platz 1, 13353, Berlin, Germany.
Nat Commun ; 13(1): 4484, 2022 08 15.
Article em En | MEDLINE | ID: mdl-35970849
ABSTRACT
Despite two years of intense global research activity, host genetic factors that predispose to a poorer prognosis of COVID-19 infection remain poorly understood. Here, we prioritise eight robust (e.g., ELF5) or suggestive but unreported (e.g., RAB2A) candidate protein mediators of COVID-19 outcomes by integrating results from the COVID-19 Host Genetics Initiative with population-based plasma proteomics using statistical colocalisation. The transcription factor ELF5 (ELF5) shows robust and directionally consistent associations across different outcome definitions, including a >4-fold higher risk (odds ratio 4.88; 95%-CI 2.47-9.63; p-value < 5.0 × 10-6) for severe COVID-19 per 1 s.d. higher genetically predicted plasma ELF5. We show that ELF5 is specifically expressed in epithelial cells of the respiratory system, such as secretory and alveolar type 2 cells, using single-cell RNA sequencing and immunohistochemistry. These cells are also likely targets of SARS-CoV-2 by colocalisation with key host factors, including ACE2 and TMPRSS2. In summary, large-scale human genetic studies together with gene expression at single-cell resolution highlight ELF5 as a risk gene for severe COVID-19, supporting a role of epithelial cells of the respiratory system in the adverse host response to SARS-CoV-2.
Assuntos

Texto completo: 1 Bases de dados: MEDLINE Assunto principal: Fatores de Transcrição / Proteínas de Ligação a DNA / COVID-19 Tipo de estudo: Etiology_studies / Prognostic_studies / Risk_factors_studies Limite: Humans Idioma: En Revista: Nat Commun Assunto da revista: BIOLOGIA / CIENCIA Ano de publicação: 2022 Tipo de documento: Article País de afiliação: Alemanha

Texto completo: 1 Bases de dados: MEDLINE Assunto principal: Fatores de Transcrição / Proteínas de Ligação a DNA / COVID-19 Tipo de estudo: Etiology_studies / Prognostic_studies / Risk_factors_studies Limite: Humans Idioma: En Revista: Nat Commun Assunto da revista: BIOLOGIA / CIENCIA Ano de publicação: 2022 Tipo de documento: Article País de afiliação: Alemanha