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

Joanita Monteiro, Franak Batliwalla, Harry Ostrer, Peter K. Gregersen

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313 Citations (Scopus)

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.

Original languageEnglish (US)
Pages (from-to)3587-3590
Number of pages4
JournalJournal of Immunology
Volume156
Issue number10
StatePublished - May 15 1996
Externally publishedYes

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Telomere Shortening
History
T-Lymphocytes
T-Lymphocyte Subsets
Cell Aging
Cell Division

ASJC Scopus subject areas

  • Immunology

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Shortened telomeres in clonally expanded CD28-CD8+ T cells imply a replicative history that is distinct from their CD28+CD8+ counterparts. / Monteiro, Joanita; Batliwalla, Franak; Ostrer, Harry; Gregersen, Peter K.

In: Journal of Immunology, Vol. 156, No. 10, 15.05.1996, p. 3587-3590.

Research output: Contribution to journalArticle

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