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A proteome-wide genetic investigation identifies several SARS-CoV-2-exploited host targets of clinical relevance.
Anisul, Mohd; Shilts, Jarrod; Schwartzentruber, Jeremy; Hayhurst, James; Buniello, Annalisa; Shaikho Elhaj Mohammed, Elmutaz; Zheng, Jie; Holmes, Michael; Ochoa, David; Carmona, Miguel; Maranville, Joseph; Gaunt, Tom R; Emilsson, Valur; Gudnason, Vilmundur; McDonagh, Ellen M; Wright, Gavin J; Ghoussaini, Maya; Dunham, Ian.
Afiliação
  • Anisul M; Wellcome Sanger Institute, Wellcome Genome Campus, Cambridge, United Kingdom.
  • Shilts J; Open Targets, Wellcome Genome Campus, Hinxton, United Kingdom.
  • Schwartzentruber J; Wellcome Sanger Institute, Wellcome Genome Campus, Cambridge, United Kingdom.
  • Hayhurst J; Wellcome Sanger Institute, Wellcome Genome Campus, Cambridge, United Kingdom.
  • Buniello A; Open Targets, Wellcome Genome Campus, Hinxton, United Kingdom.
  • Shaikho Elhaj Mohammed E; Open Targets, Wellcome Genome Campus, Hinxton, United Kingdom.
  • Zheng J; European Molecular Biology Laboratory, European Bioinformatics Institute (EMBL-EBI), Wellcome Genome Campus, Cambridge, United Kingdom.
  • Holmes M; Open Targets, Wellcome Genome Campus, Hinxton, United Kingdom.
  • Ochoa D; European Molecular Biology Laboratory, European Bioinformatics Institute (EMBL-EBI), Wellcome Genome Campus, Cambridge, United Kingdom.
  • Carmona M; Bristol-Myers Squibb, Cambridge, United States.
  • Maranville J; Medical Research Council (MRC) Integrative Epidemiology Unit, Department of Population Health Sciences, University of Bristol, Bristol, United Kingdom.
  • Gaunt TR; Clinical Trial Service Unit and Epidemiological Studies Unit (CTSU), Nuffield Department of Population Health, University of Oxford, Oxford, United Kingdom.
  • Emilsson V; Medical Research Council Population Health Research Unit (MRC PHRU), Nuffield Department of Population Health, University of Oxford, Oxford, United Kingdom.
  • Gudnason V; Open Targets, Wellcome Genome Campus, Hinxton, United Kingdom.
  • McDonagh EM; European Molecular Biology Laboratory, European Bioinformatics Institute (EMBL-EBI), Wellcome Genome Campus, Cambridge, United Kingdom.
  • Wright GJ; Open Targets, Wellcome Genome Campus, Hinxton, United Kingdom.
  • Ghoussaini M; European Molecular Biology Laboratory, European Bioinformatics Institute (EMBL-EBI), Wellcome Genome Campus, Cambridge, United Kingdom.
  • Dunham I; Bristol-Myers Squibb, Cambridge, United States.
Elife ; 102021 08 17.
Article em En | MEDLINE | ID: mdl-34402426
Individuals who become infected with the virus that causes COVID-19 can experience a wide variety of symptoms. These can range from no symptoms or minor symptoms to severe illness and death. Key demographic factors, such as age, gender and race, are known to affect how susceptible an individual is to infection. However, molecular factors, such as unique gene mutations and gene expression levels can also have a major impact on patient responses by affecting the levels of proteins in the body. Proteins that are too abundant or too scarce may mean the difference between dying from or surviving COVID-19. Identifying the molecular factors in a host that affect how viruses can infect individuals, evade immune defences or trigger severe illness, could provide new ways to treat patients with COVID-19. Such factors are likely to remain constant, even when the virus mutates into new strains. Hence, insights would likely apply across all virus strains, including current strains, such as alpha and delta, and any new strains that may emerge in the future. Using such a 'natural experiment' approach, Karim et al. compared the genetic profiles of over 30,000 COVID-19 patients and a million healthy individuals. Nine proteins were found to have an impact on COVID-19 infection and disease severity. Four proteins were ranked as top priorities for potential treatment targets. One protein, called CD209 (also known as DC-SIGN), is involved in how the virus enters the host cells, and had one of the strongest associations with COVID-19. Two proteins, called IL-6R and FAS, were involved in the immune response and could be responsible for the immune over-activation often seen in severe COVID-19. Finally, one protein, called OAS1, formed part of the body's innate antiviral defence system and appeared to reduce susceptibility to COVID-19. Knowing more about the proteins that influence the severity of COVID-19 opens up new ways to predict, protect and treat patients who may have severe or fatal reactions to infection. Indeed, one of the identified proteins (IL-6R) had already been targeted in recent clinical trials with some encouraging results. Considering CD209 as a potential receptor for the virus could provide another avenue for therapeutics, similar to previously successful approaches to block the virus' known interaction with a receptor protein. Ultimately, this research could supply an entirely new set of treatment options to help combat the COVID-19 pandemic.
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Texto completo: 1 Coleções: 01-internacional Contexto em Saúde: 2_ODS3 / 4_TD / 6_ODS3_enfermedades_notrasmisibles Base de dados: MEDLINE Assunto principal: Estudo de Associação Genômica Ampla / SARS-CoV-2 / COVID-19 Tipo de estudo: Clinical_trials / Prognostic_studies Limite: Humans Idioma: En Revista: Elife Ano de publicação: 2021 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Contexto em Saúde: 2_ODS3 / 4_TD / 6_ODS3_enfermedades_notrasmisibles Base de dados: MEDLINE Assunto principal: Estudo de Associação Genômica Ampla / SARS-CoV-2 / COVID-19 Tipo de estudo: Clinical_trials / Prognostic_studies Limite: Humans Idioma: En Revista: Elife Ano de publicação: 2021 Tipo de documento: Article