| Literature DB >> 19540809 |
Nan-Ping Weng1, Arne N Akbar, Jorg Goronzy.
Abstract
The accumulation of CD28(-) T cells, particularly within the CD8 subset, is one of the most prominent changes during T-cell homeostasis and function associated with aging in humans. CD28, a major co-stimulatory receptor, is responsible for the optimal antigen-mediated T-cell activation, proliferation and survival of T cells. CD28(-) T cells exhibit reduced antigen receptor diversity, defective antigen-induced proliferation and a shorter replicative lifespan while showing enhanced cytotoxicity and regulatory functions. Gene expression analyses reveal profound changes of CD28(-) T cells in comparison to their CD28(+) counterparts and corroborate their functional differences. Here we review recent advances in our understanding of CD28(-) T cells and their role in the age-associated decline of immune function.Entities:
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Year: 2009 PMID: 19540809 PMCID: PMC2801888 DOI: 10.1016/j.it.2009.03.013
Source DB: PubMed Journal: Trends Immunol ISSN: 1471-4906 Impact factor: 16.687