1. Human CD8+ T cells expressing HLA-DR and CD28 show telomerase activity and are distinct from cytolytic effector T cells
- Author
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Danila Valmori, Immanuel Lüscher, Mikael J. Pittet, Pedro Romero, Ferdy Lejeune, Philippe Guillaume, Marco Migliaccio, Patrick Reichenbach, Danielle Liénard, Daniel E. Speiser, and Jean-Charles Cerottini
- Subjects
ZAP70 ,Immunology ,hemic and immune systems ,chemical and pharmacologic phenomena ,Biology ,Natural killer T cell ,Molecular biology ,Interleukin 21 ,Immunology and Allergy ,Cytotoxic T cell ,Telomerase reverse transcriptase ,IL-2 receptor ,Antigen-presenting cell ,Interleukin 3 - Abstract
Cycling lymphocytes may express the enzyme telomerase which is involved in maintenance of telomere length and cell proliferation potential. In CD8(+) T cells freshly isolated from peripheral blood, we found that in vivo cycling cells expressed HLA-DR. Furthermore, CD28-positive cells are known to have longer telomeres than CD28-negative T cells. Therefore we used HLA-DR- and CD28-specific antibodies to sort CD8(+) T cells and measure telomerase activity ex vivo. Relatively high levels of telomerase activity were found in HLA-DR/CD28 double-positive cells. In contrast, HLA-DR-negative and CD28-negative cells had almost no telomerase activity. In summary, HLA-DR expression correlates with proliferation, and CD28 expression with proliferative potential. We have previously identified that ex vivo cytolytic CD8(+) T cells are CD56 (NCAM) positive. Here we show that HLA-DR(+) cells were rarely CD56(+) and vice versa. This demonstrates that telomerase-expressing and cytolytic CD8(+) T cells can be separated on the basis of the cell surface markers HLA-DR and CD56. Thus, activated CD8(+) T cells specialize and exert distinct functions correlating with surface molecule expression.
- Published
- 2001