T cell aging: naive but not young
- PMID: 15781575
- PMCID: PMC2213096
- DOI: 10.1084/jem.20050341
T cell aging: naive but not young
Abstract
The immune system exhibits profound age-related changes, collectively termed immunosenescence. The most visible of these is the decline in protective immunity, which results from a complex interaction of primary immune defects and compensatory homeostatic mechanisms. The sum of these changes is a dysregulation of many processes that normally ensure optimal immune function. Recent advances suggest that old mice can produce fully functional new T cells, opening both intriguing inquiry avenues and raising critical questions to be pursued.
References
-
- Miller, R.A. 1996. The aging immune system: primer and prospectus. Science. 273:70–74. - PubMed
-
- Wick, G., P. Jansen-Durr, P. Berger, I. Blasko, and B. Grubeck-Loebenstein. 2000. Diseases of aging. Vaccine. 18:1567–1583. - PubMed
-
- Petersen, L., A. Marfin, and D. Gubler. 2003. West Nile virus. J. AMA. 290:524–528. - PubMed
-
- Linton, P.J., and K. Dorshkind. 2004. Age-related changes in lymphocyte development and function. Nat. Immunol. 5:133–139. - PubMed
-
- Haynes, L., S.L. Swain, J. Cambier, and R. Fuldner. 2005. Aging and immune function: summary of a workshop held at Trudeau Institute, Saranac Lake, NY. Mech. Ageing Dev. In press. - PubMed
Publication types
MeSH terms
Grants and funding
LinkOut - more resources
Full Text Sources
Medical
