Ontology highlight
ABSTRACT:
ORGANISM(S): Homo sapiens
SUBMITTER: Damien Chaussabel
PROVIDER: E-GEOD-30951 | biostudies-arrayexpress |
REPOSITORIES: biostudies-arrayexpress
The Journal of experimental medicine 20110912 10
Autosomal dominant TLR3 deficiency has been identified as a genetic etiology of childhood herpes simplex virus 1 (HSV-1) encephalitis (HSE). This defect is partial, as it results in impaired, but not abolished induction of IFN-β and -λ in fibroblasts in response to TLR3 stimulation. The apparently normal resistance of these patients to other infections, viral illnesses in particular, may thus result from residual TLR3 responses. We report here an autosomal recessive form of complete TLR3 deficie ...[more]