Life-threatening influenza and impaired interferon amplification in human IRF7 deficiency

Michael J. Ciancanelli(Rockefeller University), Sarah X.L. Huang(Columbia University Irving Medical Center), Priya Luthra(Icahn School of Medicine at Mount Sinai), Hannah Garner(King's College London), Yuval Itan(Rockefeller University), Stefano Volpi(Boston Children's Hospital), Fabien G. Lafaille(Rockefeller University), Céline Trouillet(King's College London), Mirco Schmolke(Icahn School of Medicine at Mount Sinai), Randy A. Albrecht(Icahn School of Medicine at Mount Sinai), Elisabeth Israelsson(Virginia Mason Medical Center), Hye Kyung Lim(Rockefeller University), Melina Casadio(Rockefeller University), Tamar Hermesh(Rockefeller University), Lazaro Lorenzo(Inserm), Lawrence W. Leung(Icahn School of Medicine at Mount Sinai), Vincent Pedergnana(Inserm), Bertrand Boisson(Rockefeller University), Satoshi Okada(Hiroshima University), Capucine Pïcard(Inserm), B. Ringuier(Université d'Angers), Françoise Troussier(Université d'Angers), Damien Chaussabel(Virginia Mason Medical Center), Laurent Abel(Inserm), Isabelle Pellier(Centre National de la Recherche Scientifique), Luigi D. Notarangelo(Boston Children's Hospital), Adolfo García‐Sastre(Icahn School of Medicine at Mount Sinai), Christopher F. Basler(Icahn School of Medicine at Mount Sinai), Frédéric Geissmann(King's College London), Shen‐Ying Zhang(Inserm), Hans-Willem Snoeck(Columbia University Irving Medical Center), Jean‐Laurent Casanova(Howard Hughes Medical Institute)
Science
March 27, 2015
Cited by 463

Abstract

Severe influenza disease strikes otherwise healthy children and remains unexplained. We report compound heterozygous null mutations in IRF7, which encodes the transcription factor interferon regulatory factor 7, in an otherwise healthy child who suffered life-threatening influenza during primary infection. In response to influenza virus, the patient's leukocytes and plasmacytoid dendritic cells produced very little type I and III interferons (IFNs). Moreover, the patient's dermal fibroblasts and induced pluripotent stem cell (iPSC)-derived pulmonary epithelial cells produced reduced amounts of type I IFN and displayed increased influenza virus replication. These findings suggest that IRF7-dependent amplification of type I and III IFNs is required for protection against primary infection by influenza virus in humans. They also show that severe influenza may result from single-gene inborn errors of immunity.


Related Papers

No related papers found

Powered by citation graph analysis