Shortened telomeres in clonally expanded CD28-CD8+ T cells imply a replicative history that is distinct from their CD28+ CD8+ counterparts.

J Monteiro, F Batliwalla, H Ostrer… - Journal of immunology …, 1996 - journals.aai.org
J Monteiro, F Batliwalla, H Ostrer, PK Gregersen
Journal of immunology (Baltimore, Md.: 1950), 1996journals.aai.org
Long term in vitro culture of clonally expanded CD8+ T cells, generally found within the
CD57+ or CD28-subset, has generally been unsuccessful, suggesting that these cells may
have a limited replicative potential. Telomeric shortening may reflect the action of a" mitotic
clock" regulating the number of divisions a cell can undergo. In this study, we have
compared the telomeric lengths of CD28-CD8+ and CD28+ CD8+ T cells in 10 normal
individuals to assess their replicative history. Overall, the telomeric lengths were found to be …
Abstract
Long term in vitro culture of clonally expanded CD8+T cells, generally found within the CD57+ or CD28-subset, has generally been unsuccessful, suggesting that these cells may have a limited replicative potential. Telomeric shortening may reflect the action of a "mitotic clock" regulating the number of divisions a cell can undergo. In this study, we have compared the telomeric lengths of CD28-CD8+ and CD28+CD8+ T cells in 10 normal individuals to assess their replicative history. Overall, the telomeric lengths were found to be significantly shorter in the CD28-CD8+ T cell subset compared with the CD28+CD8+ subset. Furthermore, clonally expanded TCRBV11+CD8+ T cells from an individual exhibited telomeric lengths that were 2.9 kb shorter than those found in the polyclonal CD28+CD8+ T cell subset. These findings indicate that clonally expanded CD28-CD8+ T cells have undergone many more rounds of replication than CD28+CD8+ T cells, and consistent with the loss of CD28 expression, they may have reached a state of replicative senescence.
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