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• W2132969285 endingPage "42" @default.
• W2132969285 startingPage "31" @default.
• W2132969285 abstract "Summary: We have consistently observed that like other normal somatic tissue cells, human T lymphocytes manifest a finite proliferative capacity in culture in vitro. When measured in population doublings (PD), this averages about 35 PD for T-cell clones (TCC) derived from mature peripheral T cells of young adults and about 20 PD more for TCC derived from T-cell precursors in their bone marrow. We believe that alterations in surface marker phenotypes and corresponding functional changes observed in these human TCC as they progress through their finite lifespans in vitro can provide valuable information on processes of T-cell immunosenescence in vivo. They may also provide a model system for studying ways of modulating the ageing process to delay or prevent immunosenescence in the elderly and the chronically infected or possibly to accelerate immunosenescence in organ transplantation." @default.
• W2132969285 created "2016-06-24" @default.
• W2132969285 creator A5017379092 @default.
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• W2132969285 creator A5039811377 @default.
• W2132969285 creator A5067742358 @default.
• W2132969285 date "1997-12-01" @default.
• W2132969285 modified "2023-10-11" @default.
• W2132969285 title "Human T-cell clones in long-term culture as a model of immunosenescence" @default.
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• W2132969285 doi "https://doi.org/10.1111/j.1600-065x.1997.tb01025.x" @default.
• W2132969285 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/9476663" @default.
• W2132969285 hasPublicationYear "1997" @default.
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