| Literature DB >> 34822289 |
Haley E Randolph1, Jessica K Fiege2,3, Beth K Thielen4, Clayton K Mickelson2,3, Mari Shiratori5, João Barroso-Batista5, Ryan A Langlois2,3, Luis B Barreiro1,5,6.
Abstract
Humans differ in their susceptibility to infectious disease, partly owing to variation in the immune response after infection. We used single-cell RNA sequencing to quantify variation in the response to influenza infection in peripheral blood mononuclear cells from European- and African-ancestry males. Genetic ancestry effects are common but highly cell type specific. Higher levels of European ancestry are associated with increased type I interferon pathway activity in early infection, which predicts reduced viral titers at later time points. Substantial population-associated variation is explained by cis-expression quantitative trait loci that are differentiated by genetic ancestry. Furthermore, genetic ancestry–associated genes are enriched among genes correlated with COVID-19 disease severity, suggesting that the early immune response contributes to ancestry-associated differences for multiple viral infection outcomes.Entities:
Mesh:
Substances:
Year: 2021 PMID: 34822289 PMCID: PMC8957271 DOI: 10.1126/science.abg0928
Source DB: PubMed Journal: Science ISSN: 0036-8075 Impact factor: 63.714