ELF5 is a respiratory epithelial cell-specific risk gene for severe COVID-19
Maik PietzneriD, Robert Lorenz ChuaiD, Eleanor WheeleriD, Katharina JechowiD, Julian WillettiD, Helena RadbruchiD, Saskia TrumpiD, Bettina HeideckeriD, Hugo ZebergiD, Frank L. HeppneriD, Roland EilsiD, Marcus Alexander MalliD, John Brent RichardsiD, Leif Erik SanderiD, Irina LehmanniD, Soeren LukasseniD, Nicholas J. WarehamiD, Christian ConradiD, Claudia LangenbergiD
Abstract
Despite two years of intense global research activity, host genetic factors that predispose to a poorer prognosis and severe course of COVID-19 infection remain poorly understood. Here, we identified eight candidate protein mediators of COVID-19 outcomes by establishing a shared genetic architecture at protein-coding loci using large-scale human genetic studies. The transcription factor ELF5 (ELF5) showed robust and directionally consistent associations across different outcome definitions, including a >4-fold higher risk (odds ratio: 4.85; 95%-CI: 2.65-8.89; p-value<3.1x10-7) for severe COVID-19 per 1 s.d. higher genetically predicted plasma ELF5. We show that ELF5 is specifically expressed in epithelial cells of the respiratory system, such as secretory and alveolar type 2 cells, using single-cell RNA sequencing and immunohistochemistry. These cells are also likely targets of SARS-CoV-2 by colocalisation with key host factors, including ACE2 and TMPRSS2. We also observed a 25% reduced risk of severe COVID-19 per 1 s.d. higher genetically predicted plasma G-CSF, a finding corroborated by a clinical trial of recombinant human G-CSF in COVID-19 patients with lymphopenia reporting a lower number of patients developing critical illness and death. In summary, large-scale human genetic studies together with gene expression at single-cell resolution highlight ELF5 as a novel risk gene for COVID-19 prognosis, supporting a role of epithelial cells of the respiratory system in the adverse host response to SARS-CoV-2.
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