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Abstract
Objective: To determine the proportion of children with herpes simplex encephalitis (HSE) displaying TLR3 deficiency, the extent of TLR3 allelic heterogeneity, and the specific clinical features of TLR3 deficiency.
Methods: We determined the sequence of all exons of TLR3 in 110 of the 120 patients with HSE enrolled in our study who do not carry any of the previously described HSE-predisposing mutations of TLR3 pathway genes (TLR3, UNC93B1, TRIF, TRAF3, and TBK1). All the new mutant TLR3 alleles detected were characterized experimentally in-depth to establish the causal relationship between the genotype and phenotype.
Results: In addition to the 3 previously reported TLR3-deficient patients from the same cohort, 6 other children or young adults with HSE carry 1 of 5 unique or extremely rare (minor allele frequency <0.001) missense TLR3 alleles. Two alleles (M374T, D592N) heterozygous in 3 patients are not deleterious in vitro. The other 3 are deleterious via different mechanisms: G743D+R811I and L360P heterozygous in 2 patients are loss-of-function due to low levels of expression and lack of cleavage, respectively, and R867Q homozygous in 1 patient is hypomorphic. The 3 patients' fibroblasts display impaired TLR3 responses and enhanced herpes simplex virus 1 susceptibility. Overall, TLR3 deficiency is therefore found in 6 (5%) of the 120 patients studied. There is high allelic heterogeneity, with 3 forms of autosomal dominant partial defect by negative dominance or haploinsufficiency, and 2 forms of autosomal recessive defect with complete or partial deficiency. Finally, 4 (66%) of the 6 TLR3-deficient patients had at least 1 late relapse of HSE, whereas relapse occurred in only 12 (10%) of the total cohort of 120 patients.
Conclusions: Childhood-onset HSE is due to TLR3 deficiency in a traceable fraction of patients, in particular the ones with HSE recurrence. Mutations in TLR3 and TLR3 pathway genes should be searched and experimentally studied in children with HSE, and patients with proven TLR3 deficiency should be followed carefully.
GLOSSARY
- AD=
- autosomal dominant;
- AR=
- autosomal recessive;
- CEPH-HGDP=
- Centre d'Etude du Polymorphisme Humain–Human Genome Diversity Project;
- dbSNP=
- Single Nucleotide Polymorphism database;
- DN=
- dominant negative;
- ds=
- double-stranded;
- ECD=
- ectodomain;
- GFP=
- green fluorescent protein;
- HA=
- hemagglutinin;
- HSE=
- herpes simplex encephalitis;
- HSV-1=
- herpes simplex virus 1;
- IFN=
- interferon;
- iPSC=
- induced pluripotent stem cell;
- poly(I:C)=
- polyinosine:polycytidylic acid;
- TIR=
- Toll/interleukin-1 receptor;
- VSV=
- vesicular stomatitis virus;
- WES=
- whole-exome sequencing;
- WT=
- wild-type
Footnotes
↵* These authors contributed equally to this work.
Go to Neurology.org for full disclosures. Funding information and disclosures deemed relevant by the authors, if any, are provided at the end of the article.
Editorial, page 1882
Supplemental data at Neurology.org
- Received January 7, 2014.
- Accepted in final form June 23, 2014.
- © 2014 American Academy of Neurology
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