TLR3 Deficiency in Patients with Herpes Simplex Encephalitis

2007 Science 1,107 citations

Abstract

Some Toll and Toll-like receptors (TLRs) provide immunity to experimental infections in animal models, but their contribution to host defense in natural ecosystems is unknown. We report a dominant-negative TLR3 allele in otherwise healthy children with herpes simplex virus 1 (HSV-1) encephalitis. TLR3 is expressed in the central nervous system (CNS), where it is required to control HSV-1, which spreads from the epithelium to the CNS via cranial nerves. TLR3 is also expressed in epithelial and dendritic cells, which apparently use TLR3-independent pathways to prevent further dissemination of HSV-1 and to provide resistance to other pathogens in TLR3-deficient patients. Human TLR3 appears to be redundant in host defense to most microbes but is vital for natural immunity to HSV-1 in the CNS, which suggests that neurotropic viruses have contributed to the evolutionary maintenance of TLR3.

Keywords

TLR3EncephalitisImmunologyHerpes simplex virusBiologyImmunityVirologyVirusInnate immune systemCentral nervous systemImmune systemToll-like receptorNeuroscience

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Publication Info

Year
2007
Type
article
Volume
317
Issue
5844
Pages
1522-1527
Citations
1107
Access
Closed

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Shen‐Ying Zhang, Emmanuelle Jouanguy, Sophie Ugolini et al. (2007). TLR3 Deficiency in Patients with Herpes Simplex Encephalitis. Science , 317 (5844) , 1522-1527. https://doi.org/10.1126/science.1139522

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DOI
10.1126/science.1139522