Journal

Journal of immunology (Baltimore, Md. : 1950)
ISSN: 1550-6606
Titre abrégé: J Immunol
Pays: United States
ID NLM: 2985117R

Informations de publication

Date de publication:
01 03 2019
Historique:
received: 16 01 2018
accepted: 21 12 2018
pubmed: 27 1 2019
medline: 13 11 2019
entrez: 27 1 2019
Statut: ppublish

Résumé

Herpes simplex encephalitis (HSE), caused by HSV type 1 (HSV-1) infection, is an acute neuroinflammatory condition of the CNS and remains the most common type of sporadic viral encephalitis worldwide. Studies in humans have shown that susceptibility to HSE depends in part on the genetic make-up of the host, with deleterious mutations in the TLR3/type I IFN axis underlying some cases of childhood HSE. Using an in vivo chemical mutagenesis screen for HSV-1 susceptibility in mice, we identified a susceptible pedigree carrying a causal truncating mutation in the

Identifiants

pubmed: 30683700
pii: jimmunol.1800063
doi: 10.4049/jimmunol.1800063
doi:

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

1479-1493

Subventions

Organisme : CIHR
ID : CTP-87520
Pays : Canada
Organisme : CIHR
ID : MOP-238757
Pays : Canada

Informations de copyright

Copyright © 2019 by The American Association of Immunologists, Inc.

Auteurs

Mathieu Mancini (M)

Department of Human Genetics, McGill University, Montreal, Quebec H3A 0C7, Canada.
McGill Research Centre on Complex Traits, McGill University, Montreal, Quebec H3G 0B1, Canada.

Grégory Caignard (G)

Department of Human Genetics, McGill University, Montreal, Quebec H3A 0C7, Canada.
Laboratoire de Santé Animale d'Alfort, Université Paris Est, Agence Nationale de Sécurité Sanitaire de l'Alimentation, de l'Environnement et du Travail, École Nationale Vétérinaire d'Alfort, Institut National de la Recherche Agronomique, UMR 1161 Virologie, 94706 Maisons-Alfort, France.

Benoît Charbonneau (B)

Department of Human Genetics, McGill University, Montreal, Quebec H3A 0C7, Canada.
McGill Research Centre on Complex Traits, McGill University, Montreal, Quebec H3G 0B1, Canada.

Anne Dumaine (A)

Department of Human Genetics, McGill University, Montreal, Quebec H3A 0C7, Canada.
McGill Research Centre on Complex Traits, McGill University, Montreal, Quebec H3G 0B1, Canada.

Nila Wu (N)

Department of Human Genetics, McGill University, Montreal, Quebec H3A 0C7, Canada.
McGill Research Centre on Complex Traits, McGill University, Montreal, Quebec H3G 0B1, Canada.

Gabriel A Leiva-Torres (GA)

Department of Human Genetics, McGill University, Montreal, Quebec H3A 0C7, Canada.
McGill Research Centre on Complex Traits, McGill University, Montreal, Quebec H3G 0B1, Canada.

Steve Gerondakis (S)

Biomedicine Discovery Institute, Monash University, Clayton, Victoria 3800, Australia.
Department of Biochemistry and Molecular Biology, Monash University, Clayton, Victoria 3800, Australia.

Angela Pearson (A)

Institut National de la Recherche Scientifique-Institut Armand-Frappier, Laval, Quebec H7V 1B7, Canada.

Salman T Qureshi (ST)

McGill Research Centre on Complex Traits, McGill University, Montreal, Quebec H3G 0B1, Canada.
Division of Experimental Medicine, Department of Medicine, McGill University, Montreal, Quebec H4A 3J1, Canada; and.

Robert Sladek (R)

Department of Human Genetics, McGill University, Montreal, Quebec H3A 0C7, Canada.
McGill University and Genome Québec Innovation Centre, Montreal, Quebec H3A 0G1, Canada.

Silvia M Vidal (SM)

Department of Human Genetics, McGill University, Montreal, Quebec H3A 0C7, Canada; silvia.vidal@mcgill.ca.
McGill Research Centre on Complex Traits, McGill University, Montreal, Quebec H3G 0B1, Canada.

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Classifications MeSH