COVID-19 and systemic lupus erythematosus genetics: A balance between autoimmune disease risk and protection against infection |
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Authors: | Yuxuan Wang Suri Guga Kejia Wu Zoe Khaw Konstantinos Tzoumkas Phil Tombleson Mary E. Comeau Carl D. Langefeld Deborah S. Cunninghame Graham David L. Morris Timothy J. Vyse |
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Affiliation: | 1. Department of Medical & Molecular Genetics, King’s College London, London, United Kingdom;2. NIHR GSTFT/KCL Biomedical Research Centre, London, United Kingdom;3. 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; University of Pennsylvania, UNITED STATES |
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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. |
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