| Literature DB >> 15520850 |
Stefanie Sarantopoulos1, Linrong Lu, Harvey Cantor.
Abstract
There is increasing evidence that the immune response can be inhibited by several T cell subsets, including NK T cells, CD25+CD4+ T cells, and a subpopulation of CD8+ T cells. Animal model studies of multiple sclerosis have suggested an important role for suppressor CD8+ T cells in protection against disease recurrence and exacerbation. The molecular lynchpin of CD8+ suppressive activity is the murine MHC molecule Qa-1, termed HLA-E in humans. Here we summarize findings from work on Qa-1 that have begun to delineate suppressor CD8+ T cells and their mechanisms of action in the context of self tolerance and autoimmune disease.Entities:
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Year: 2004 PMID: 15520850 PMCID: PMC524234 DOI: 10.1172/JCI23152
Source DB: PubMed Journal: J Clin Invest ISSN: 0021-9738 Impact factor: 14.808