Herpes simplex virus encephalitis in a patient with complete TLR3 deficiency: TLR3 is otherwise redundant in protective immunity

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 n...

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Detalles Bibliográficos
Autores principales: Guo, Yiqi, Audry, Magali, Ciancanelli, Michael, Alsina, Laia, Azevedo, Joana, Herman, Melina, Anguiano, Esperanza, Sancho-Shimizu, Vanessa, Lorenzo, Lazaro, Pauwels, Elodie, Philippe, Paul Bastard, Pérez de Diego, Rebeca, Cardon, Annabelle, Vogt, Guillaume, Picard, Capucine, Andrianirina, Zafitsara Zo, Rozenberg, Flore, Lebon, Pierre, Plancoulaine, Sabine, Tardieu, Marc, Valérie Doireau, Jouanguy, Emmanuelle, Chaussabel, Damien, Geissmann, Frederic, Abel, Laurent, Casanova, Jean-Laurent, Zhang, Shen-Ying
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Rockefeller University Press 2011
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3182056/
https://www.ncbi.nlm.nih.gov/pubmed/21911422
http://dx.doi.org/10.1084/jem.20101568

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3182056/
https://www.ncbi.nlm.nih.gov/pubmed/21911422
http://dx.doi.org/10.1084/jem.20101568

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