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CD1d Expression and Invariant NKT Cell Responses in Herpesvirus Infections.
Chung, Brian K; Priatel, John J; Tan, Rusung.
Afiliación
  • Chung BK; NIHR Birmingham Liver Biomedical Research Unit, Centre for Liver Research, University of Birmingham , Birmingham , UK ; Institute of Clinical Medicine, Faculty of Medicine, University of Oslo , Oslo , Norway.
  • Priatel JJ; Department of Pathology and Laboratory Medicine, University of British Columbia , Vancouver, BC , Canada.
  • Tan R; Department of Pathology, Sidra Medical and Research Center , Doha , Qatar.
Front Immunol ; 6: 312, 2015.
Article en En | MEDLINE | ID: mdl-26161082
ABSTRACT
Invariant natural killer T (iNKT) cells are a highly conserved subset of unconventional T lymphocytes that express a canonical, semi-invariant T cell receptor and surface markers shared with the natural killer cell lineage. iNKT cells recognize exogenous and endogenous glycolipid antigens restricted by non-polymorphic CD1d molecules, and are highly responsive to the prototypical agonist, α-galactosylceramide. Upon activation, iNKT cells rapidly coordinate signaling between innate and adaptive immune cells through the secretion of proinflammatory cytokines, leading to the maturation of antigen-presenting cells, and expansion of antigen-specific CD4+ and CD8+ T cells. Because of their potent immunoregulatory properties, iNKT cells have been extensively studied and are known to play a pivotal role in mediating immune responses against microbial pathogens including viruses. Here, we review evidence that herpesviruses manipulate CD1d expression to escape iNKT cell surveillance and establish lifelong latency in humans. Collectively, published findings suggest that iNKT cells play critical roles in anti-herpesvirus immune responses and could be harnessed therapeutically to limit viral infection and viral-associated disease.
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Idioma: En Revista: Front Immunol Año: 2015 Tipo del documento: Article País de afiliación: Noruega

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Idioma: En Revista: Front Immunol Año: 2015 Tipo del documento: Article País de afiliación: Noruega