| Literature DB >> 28368532 |
Manuela Sironi1, Anna Maria Peri2, Rachele Cagliani1, Diego Forni1, Stefania Riva1, Mara Biasin3, Mario Clerici4,5, Andrea Gori2.
Abstract
Defects in genes of the Toll-like receptor 3 (TLR3) pathway are associated with susceptibility to herpes simplex virus type 1 encephalitis (HSE). We analyzed a cohort of 11 adult Italian patients in whom viral encephalitis developed. We detected 2 rare missense mutations in TLR3: 1 in a patient with HSE (p.Leu297Val) and 1 in a patient with varicella-zoster virus encephalitis (p.Leu199Phe). Both mutations are extremely rare in human populations and have pathogenicity scores highly suggestive of a functional effect. Data herein expand the phenotypic spectrum of TLR3 mutations to varicella-zoster virus encephalitis and support the role of TLR3 genetic defects as risk factors for HSE in adults.Entities:
Keywords: TLR3; adult patients.; herpes simplex virus encephalitis; varicella-zoster virus encephalitis
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Year: 2017 PMID: 28368532 DOI: 10.1093/infdis/jix166
Source DB: PubMed Journal: J Infect Dis ISSN: 0022-1899 Impact factor: 5.226