A detrimental role for invariant natural ...
Type de document :
Compte-rendu et recension critique d'ouvrage
PMID :
Titre :
A detrimental role for invariant natural killer T cells in the pathogenesis of experimental dengue virus infection
Auteur(s) :
Renneson, Joelle [Auteur]
Centre d’Infection et d’Immunité de Lille - INSERM U 1019 - UMR 9017 - UMR 8204 [CIIL]
Institut Pasteur de Lille
Guabiraba, Rodrigo [Auteur]
Infectiologie Animale et Santé Publique [UR IASP]
Universidade Federal de Minas Gerais = Federal University of Minas Gerais [Belo Horizonte, Brazil] [UFMG]
Maillet, Isabelle [Auteur]
Immunologie et Embryologie Moléculaires [IEM]
Marques, Rafael E. [Auteur]
Universidade Federal de Minas Gerais = Federal University of Minas Gerais [Belo Horizonte, Brazil] [UFMG]
Ivanov, Stoyan [Auteur]
Centre d’Infection et d’Immunité de Lille - INSERM U 1019 - UMR 9017 - UMR 8204 [CIIL]
Institut Pasteur de Lille
Fontaine, Josette [Auteur]
Institut Pasteur de Lille
Paget, Christophe [Auteur]
Institut Pasteur de Lille
Quesniaux, Valérie [Auteur]
Immunologie et Embryologie Moléculaires [IEM]
Faveeuw, Christelle [Auteur]
Institut Pasteur de Lille
Ryffel, Bernhard [Auteur]
Immunologie et Embryologie Moléculaires [IEM]
Teixeira, Mauro M. [Auteur]
Universidade Federal de Minas Gerais = Federal University of Minas Gerais [Belo Horizonte, Brazil] [UFMG]
Trottein, Francois [Auteur correspondant]
Institut Pasteur de Lille
Centre d’Infection et d’Immunité de Lille - INSERM U 1019 - UMR 9017 - UMR 8204 [CIIL]
Institut Pasteur de Lille
Guabiraba, Rodrigo [Auteur]
Infectiologie Animale et Santé Publique [UR IASP]
Universidade Federal de Minas Gerais = Federal University of Minas Gerais [Belo Horizonte, Brazil] [UFMG]
Maillet, Isabelle [Auteur]
Immunologie et Embryologie Moléculaires [IEM]
Marques, Rafael E. [Auteur]
Universidade Federal de Minas Gerais = Federal University of Minas Gerais [Belo Horizonte, Brazil] [UFMG]
Ivanov, Stoyan [Auteur]
Centre d’Infection et d’Immunité de Lille - INSERM U 1019 - UMR 9017 - UMR 8204 [CIIL]
Institut Pasteur de Lille
Fontaine, Josette [Auteur]
Institut Pasteur de Lille
Paget, Christophe [Auteur]
Institut Pasteur de Lille
Quesniaux, Valérie [Auteur]
Immunologie et Embryologie Moléculaires [IEM]
Faveeuw, Christelle [Auteur]
Institut Pasteur de Lille
Ryffel, Bernhard [Auteur]
Immunologie et Embryologie Moléculaires [IEM]
Teixeira, Mauro M. [Auteur]
Universidade Federal de Minas Gerais = Federal University of Minas Gerais [Belo Horizonte, Brazil] [UFMG]
Trottein, Francois [Auteur correspondant]
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Institut Pasteur de Lille
Titre de la revue :
AMERICAN JOURNAL OF PATHOLOGY
Pagination :
1872-1883
Éditeur :
American Society for Investigative Pathology / Elsevier
Date de publication :
2011
ISSN :
0002-9440
Discipline(s) HAL :
Sciences du Vivant [q-bio]/Immunologie
Résumé en anglais : [en]
Dengue virus (DENV), a member of the mosquito-borne flaviviruses, is a serious public health problem in many tropical countries. We assessed the in vivo physiologic contribution of invariant natural killer T (iNKT) cells, ...
Lire la suite >Dengue virus (DENV), a member of the mosquito-borne flaviviruses, is a serious public health problem in many tropical countries. We assessed the in vivo physiologic contribution of invariant natural killer T (iNKT) cells, a population of nonconventional lipid-reactive alphabeta T lymphocytes, to the host response during experimental DENV infection. We used a mouse-adapted DENV serotype 2 strain that causes a disease that resembles severe dengue in humans. On DENV challenge, splenic and hepatic iNKT cells became activated insofar as CD69 and Fas ligand up-regulation and interferon-gamma production. C57BL/6 mice deficient in iNKT cells (Jalpha18(-/-)) were more resistant to lethal infection than were wild-type animals, and the phenotype was reversed by adoptive transfer of iNKT cells to Jalpha18(-/-) animals. The absence of iNKT cells in Jalpha18(-/-) mice was associated with decreased systemic and local inflammatory responses, less liver injury, diminished vascular leak syndrome, and reduced activation of natural killer cells and neutrophils. iNKT cell functions were not necessary for control of primary DENV infection, after either natural endogenous activation or exogenous activation with the canonical iNKT cell agonist alpha-galactosylceramide. Together, these data reveal a novel and critical role for iNKT cells in the pathogenesis of severe experimental dengue disease.Lire moins >
Lire la suite >Dengue virus (DENV), a member of the mosquito-borne flaviviruses, is a serious public health problem in many tropical countries. We assessed the in vivo physiologic contribution of invariant natural killer T (iNKT) cells, a population of nonconventional lipid-reactive alphabeta T lymphocytes, to the host response during experimental DENV infection. We used a mouse-adapted DENV serotype 2 strain that causes a disease that resembles severe dengue in humans. On DENV challenge, splenic and hepatic iNKT cells became activated insofar as CD69 and Fas ligand up-regulation and interferon-gamma production. C57BL/6 mice deficient in iNKT cells (Jalpha18(-/-)) were more resistant to lethal infection than were wild-type animals, and the phenotype was reversed by adoptive transfer of iNKT cells to Jalpha18(-/-) animals. The absence of iNKT cells in Jalpha18(-/-) mice was associated with decreased systemic and local inflammatory responses, less liver injury, diminished vascular leak syndrome, and reduced activation of natural killer cells and neutrophils. iNKT cell functions were not necessary for control of primary DENV infection, after either natural endogenous activation or exogenous activation with the canonical iNKT cell agonist alpha-galactosylceramide. Together, these data reveal a novel and critical role for iNKT cells in the pathogenesis of severe experimental dengue disease.Lire moins >
Langue :
Anglais
Vulgarisation :
Non
Commentaire :
Renneson, Joelle Guabiraba, Rodrigo Maillet, Isabelle Marques, Rafael E Ivanov, Stoyan Fontaine, Josette Paget, Christophe Quesniaux, Valerie Faveeuw, Christelle Ryffel, Bernhard Teixeira, Mauro M Trottein, Francois Am J Pathol. 2011 Oct;179(4):1872-83. doi: 10.1016/j.ajpath.2011.06.023. Epub 2011 Aug 16.
Source :
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- https://doi.org/10.1016/j.ajpath.2011.06.023
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- https://doi.org/10.1016/j.ajpath.2011.06.023
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- https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3181339/pdf
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