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COVID-19 and systemic lupus erythematosus genetics: A balance between autoimmune disease risk and protection against infection.
Wang, Yuxuan; Guga, Suri; Wu, Kejia; Khaw, Zoe; Tzoumkas, Konstantinos; Tombleson, Phil; Comeau, Mary E; Langefeld, Carl D; Cunninghame Graham, Deborah S; Morris, David L; Vyse, Timothy J.
Afiliação
  • Wang Y; Department of Medical & Molecular Genetics, King's College London, London, United Kingdom.
  • Guga S; Department of Medical & Molecular Genetics, King's College London, London, United Kingdom.
  • Wu K; Department of Medical & Molecular Genetics, King's College London, London, United Kingdom.
  • Khaw Z; Department of Medical & Molecular Genetics, King's College London, London, United Kingdom.
  • Tzoumkas K; Department of Medical & Molecular Genetics, King's College London, London, United Kingdom.
  • Tombleson P; NIHR GSTFT/KCL Biomedical Research Centre, London, United Kingdom.
  • Comeau ME; Department of Biostatistics and Data Science and Center for Precision Medicine, Wake Forest University School of Medicine, Winston-Salem, North Carolina, United States of America.
  • Langefeld CD; Department of Biostatistics and Data Science and Center for Precision Medicine, Wake Forest University School of Medicine, Winston-Salem, North Carolina, United States of America.
  • Cunninghame Graham DS; Department of Medical & Molecular Genetics, King's College London, London, United Kingdom.
  • Morris DL; Department of Medical & Molecular Genetics, King's College London, London, United Kingdom.
  • Vyse TJ; Department of Medical & Molecular Genetics, King's College London, London, United Kingdom.
PLoS Genet ; 18(11): e1010253, 2022 11.
Article em En | MEDLINE | ID: mdl-36327221
ABSTRACT
Genome wide association studies show there is a genetic component to severe COVID-19. We find evidence that the genome-wide genetic association signal with severe COVID-19 is correlated with that of systemic lupus erythematosus (SLE), having formally tested this using genetic correlation analysis by LD score regression. To identify the shared associated loci and gain insight into the shared genetic effects, using summary level data we performed meta-analyses, a local genetic correlation analysis and fine-mapping using stepwise regression and functional annotation. This identified multiple loci shared between the two traits, some of which exert opposing effects. The locus with most evidence of shared association is TYK2, a gene critical to the type I interferon pathway, where the local genetic correlation is negative. Another shared locus is CLEC1A, where the direction of effects is aligned, that encodes a lectin involved in cell signaling, and the anti-fungal immune response. Our analyses suggest that several loci with reciprocal effects between the two traits have a role in the defense response pathway, adding to the evidence that SLE risk alleles are protective against infection.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Doenças Autoimunes / COVID-19 / Lúpus Eritematoso Sistêmico Tipo de estudo: Etiology_studies / Prognostic_studies / Risk_factors_studies Limite: Humans Idioma: En Revista: PLoS Genet Assunto da revista: GENETICA Ano de publicação: 2022 Tipo de documento: Article País de afiliação: Reino Unido

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Doenças Autoimunes / COVID-19 / Lúpus Eritematoso Sistêmico Tipo de estudo: Etiology_studies / Prognostic_studies / Risk_factors_studies Limite: Humans Idioma: En Revista: PLoS Genet Assunto da revista: GENETICA Ano de publicação: 2022 Tipo de documento: Article País de afiliação: Reino Unido