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Human SNP links differential outcomes in inflammatory and infectious disease to a FOXO3-Regulated Pathway

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Authors

Lee, James C
Espeli, Marion
Anderson, Carl A
Linterman, Michelle
Pocock, Joanna M
Williams, Naomi J
Roberts, Rebecca
Viatte, Sebastien
Fu, Bo
Peshu, Norbert

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Elsevier

Abstract

The clinical course and eventual outcome, or prognosis, of complex diseases varies enormously between affected individuals. This variability critically determines the impact a disease has on a patient’s life but is very poorly understood. Here, we exploit existing genome-wide association study data to gain insight into the role of genetics in prognosis. We identify a noncoding polymorphism in FOXO3A (rs12212067: T > G) at which the minor (G) allele, despite not being associated with disease susceptibility, is associated with a milder course of Crohn’s disease and rheumatoid arthritis and with increased risk of severe malaria. Minor allele carriage is shown to limit inflammatory responses in monocytes via a FOXO3-driven pathway, which through TGFb1 reduces production of proinflammatory cytokines, including TNFa, and increases production of anti-inflammatory cytokines, including IL-10. Thus, we uncover a shared genetic contribution to prognosis in distinct diseases that operates via a FOXO3-driven pathway modulating inflammatory responses.

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Cell 155 (2013): 57-69

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