Mg 2+ Regulates Cytotoxic Functions of NK and CD8 T Cells in Chronic EBV Infection Through NKG2D

Autor: Amber N. Shatzer, Gulbu Uzel, Stefania Pittaluga, Rebecca A. Marsh, Feng-Yen Li, Jack J. Bleesing, Jeffrey I. Cohen, Ping Jiang, Timothy Jancel, Geraldine M. O’Connor, Helen F. Matthews, Huseyin Mehmet, Michael J. Lenardo, Taco W. Kuijpers, Matthew Biancalana, Kim E. Nichols, Benjamin Chaigne-Delalande, Sunil Nagpal, Marshall J. Lukacs, Lixin Zheng, Helen C. Su, Carrie L. Lucas
Přispěvatelé: AII - Amsterdam institute for Infection and Immunity, Paediatric Infectious Diseases / Rheumatology / Immunology
Rok vydání: 2013
Předmět:
Zdroj: Science, 341(6142), 186-191. American Association for the Advancement of Science
ISSN: 1095-9203
0036-8075
Popis: Magnesium to the Rescue Individuals with X-linked immunodeficiency with Mg 2+ defect, Epstein-Barr virus (EBV) infection, and neoplasia (XMEN) disease are genetically deficient for expression of MAGT1 , a magnesium transporter. Chaigne-Delalande et al. (p. 186 ) sought to better understand why these individuals are chronically infected with EBV at high viral loads and are susceptible to the development of lymphomas. CD8 + T cells and natural killer cells, which help to keep EBV infection in check, exhibited reduced cytotoxicity owing to their lower expression of the cell surface receptor NKG2D, which triggers cytolysis upon ligation. Magnesium supplementation in vitro and also in two XMEN patients restored levels of free Mg 2+ , increased NKG2D expression, and resulted in reduced amounts of EBV + cells, suggesting that this may be an effective therapeutic approach for XMEN patients.
Databáze: OpenAIRE