A highly prevalent lupus risk haplotype increases IRF7-dependent induction of IFN-alpha enhancing antiviral defense and exacerbating autoimmunity

Statistical fine mapping prioritizes a highly prevalent coding haplotype within the IRF7 gene. Analysis of ancient DNA confirms that this risk haplotype has persisted at high frequencies in the global population for millennia.

The IRF7 risk haplotype is sufficient to increase nuclear localization of IRF7 and transcriptional activity downstream of pattern recognition receptor pathways. This risk haplotype increased binding strength and altered sequence specificity of IRF7 interactions with DNA, resulting in genotype-dependent increases in IFN-a production in numerous biological systems, including monocytes and airway epithelial cells. CRISPR engineering of a homologous risk variant in mouse Irf7 results in both enhanced innate control virus infection and increased autoantibody titers in a model of autoimmunity.