Publikation: Bidrag til tidsskrift/Konferencebidrag i tidsskrift /Bidrag til avis › Tidsskriftartikel › Forskning › peer review
Defective interferon priming and impaired antiviral responses in a patient with an IRF7 variant and severe influenza. / Thomsen, Michelle M; Jørgensen, Sofie E; Gad, Hans Henrik; Storgaard, Merete; Gjedsted, Jakob; Christiansen, Mette; Hartmann, Rune; Mogensen, Trine H.
I: Medical Microbiology and Immunology, Bind 208, Nr. 6, 12.2019, s. 869-876.Publikation: Bidrag til tidsskrift/Konferencebidrag i tidsskrift /Bidrag til avis › Tidsskriftartikel › Forskning › peer review
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TY - JOUR
T1 - Defective interferon priming and impaired antiviral responses in a patient with an IRF7 variant and severe influenza
AU - Thomsen, Michelle M
AU - Jørgensen, Sofie E
AU - Gad, Hans Henrik
AU - Storgaard, Merete
AU - Gjedsted, Jakob
AU - Christiansen, Mette
AU - Hartmann, Rune
AU - Mogensen, Trine H
PY - 2019/12
Y1 - 2019/12
N2 - Influenza infection is common worldwide with many individuals affected each year during epidemics and occasionally pandemics. Previous studies in animal models and a few human cases have established an important role of innate type I and III interferon (IFN) for viral elimination and mounting of antiviral responses. However, genetic and immunological determinants of very severe disseminated influenza virus infection in humans remain incompletely understood. Here, we describe an adult patient with severe influenza virus A (IAV) infection, in whom we identified a rare variant E331V in IFN regulatory factor (IRF)7 by whole-exome sequencing. Examination of patient cells demonstrated a cellular phenotype suggesting functional IRF7 impairment, since priming with IFN was almost abolished and IFN responses to IAV were significantly impaired in patient cells. Moreover, IAV replication was significantly higher in patient cells than in controls. Finally, expression of IRF7 E331V in HEK293 cells demonstrated significantly reduced activation of both IFNA7 and IFNB promoters in a luciferase reporter gene expression assay compared to IRF7 wild type. These findings provide further support for the essential role of IRF7 in amplifying antiviral IFN responses to ensure potent and sustained IFN responses during influenza virus infection in humans.
AB - Influenza infection is common worldwide with many individuals affected each year during epidemics and occasionally pandemics. Previous studies in animal models and a few human cases have established an important role of innate type I and III interferon (IFN) for viral elimination and mounting of antiviral responses. However, genetic and immunological determinants of very severe disseminated influenza virus infection in humans remain incompletely understood. Here, we describe an adult patient with severe influenza virus A (IAV) infection, in whom we identified a rare variant E331V in IFN regulatory factor (IRF)7 by whole-exome sequencing. Examination of patient cells demonstrated a cellular phenotype suggesting functional IRF7 impairment, since priming with IFN was almost abolished and IFN responses to IAV were significantly impaired in patient cells. Moreover, IAV replication was significantly higher in patient cells than in controls. Finally, expression of IRF7 E331V in HEK293 cells demonstrated significantly reduced activation of both IFNA7 and IFNB promoters in a luciferase reporter gene expression assay compared to IRF7 wild type. These findings provide further support for the essential role of IRF7 in amplifying antiviral IFN responses to ensure potent and sustained IFN responses during influenza virus infection in humans.
KW - IRF7
KW - Influenza virus
KW - Innate immunity
KW - Interferon
KW - Primary immunodeficiency
U2 - 10.1007/s00430-019-00623-8
DO - 10.1007/s00430-019-00623-8
M3 - Journal article
C2 - 31172279
VL - 208
SP - 869
EP - 876
JO - Medical Microbiology and Immunology
JF - Medical Microbiology and Immunology
SN - 0300-8584
IS - 6
ER -