Herpes Simplex Virus Encephalitis in Human UNC-93B Deficiency

Armanda Casrouge(Délégation Paris 5), Shen‐Ying Zhang(Délégation Paris 5), Céline Eidenschenk(Délégation Paris 5), Emmanuelle Jouanguy(Délégation Paris 5), Anne Puel(Délégation Paris 5), Kun Yang(Délégation Paris 5), Alexandre Alcaïs(Délégation Paris 5), Capucine Pïcard(Délégation Paris 5), Nora Mahfoufi(Délégation Paris 5), Nathalie Nicolas(Délégation Paris 5), Lazaro Lorenzo(Délégation Paris 5), Sabine Plancoulaine(Délégation Paris 5), Brigitte Sénéchal(Délégation Paris 5), Frédéric Geissmann(Délégation Paris 5), Koichi Tabeta(Délégation Paris 5), Kasper Hoebe(Délégation Paris 5), Xin Du(Délégation Paris 5), Richard L. Miller(Délégation Paris 5), Bénédicte Héron(Délégation Paris 5), Cyril Mignot(Délégation Paris 5), Thierry Billette de Villemeur(Délégation Paris 5), Pierre Lebon(Délégation Paris 5), Olivier Dulac(Délégation Paris 5), Flore Rozenberg(Délégation Paris 5), Bruce Beutler(Délégation Paris 5), Marc Tardieu(Délégation Paris 5), Laurent Abel(Délégation Paris 5), Jean‐Laurent Casanova(Délégation Paris 5)
Science
September 14, 2006
Cited by 757

Abstract

Herpes simplex virus-1 (HSV-1) encephalitis (HSE) is the most common form of sporadic viral encephalitis in western countries. Its pathogenesis remains unclear, as it affects otherwise healthy patients and only a small minority of HSV-1-infected individuals. Here, we elucidate a genetic etiology for HSE in two children with autosomal recessive deficiency in the intracellular protein UNC-93B, resulting in impaired cellular interferon-alpha/beta and -lambda antiviral responses. HSE can result from a single-gene immunodeficiency that does not compromise immunity to most pathogens, unlike most known primary immunodeficiencies. Other severe infectious diseases may also reflect monogenic disorders of immunity.


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