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COVID-19 and systemic lupus erythematosus genetics: A balance between autoimmune disease risk and protection against infection
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...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9632821/ https://www.ncbi.nlm.nih.gov/pubmed/36327221 http://dx.doi.org/10.1371/journal.pgen.1010253 |
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author | 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. |
author_facet | 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. |
author_sort | Wang, Yuxuan |
collection | PubMed |
description | 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. |
format | Online Article Text |
id | pubmed-9632821 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-96328212022-11-04 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. PLoS Genet Research Article 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. Public Library of Science 2022-11-03 /pmc/articles/PMC9632821/ /pubmed/36327221 http://dx.doi.org/10.1371/journal.pgen.1010253 Text en © 2022 Wang et al https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Article 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. COVID-19 and systemic lupus erythematosus genetics: A balance between autoimmune disease risk and protection against infection |
title | COVID-19 and systemic lupus erythematosus genetics: A balance between autoimmune disease risk and protection against infection |
title_full | COVID-19 and systemic lupus erythematosus genetics: A balance between autoimmune disease risk and protection against infection |
title_fullStr | COVID-19 and systemic lupus erythematosus genetics: A balance between autoimmune disease risk and protection against infection |
title_full_unstemmed | COVID-19 and systemic lupus erythematosus genetics: A balance between autoimmune disease risk and protection against infection |
title_short | COVID-19 and systemic lupus erythematosus genetics: A balance between autoimmune disease risk and protection against infection |
title_sort | covid-19 and systemic lupus erythematosus genetics: a balance between autoimmune disease risk and protection against infection |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9632821/ https://www.ncbi.nlm.nih.gov/pubmed/36327221 http://dx.doi.org/10.1371/journal.pgen.1010253 |
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