Virus-induced CD8+ T cell clonal expansion is associated with telomerase up-regulation and telomere length preservation: a mechanism for rescue from replicative senescence.

In acute infectious mononucleosis (AIM), very large clones of Ag-specific CD8+ effector T cells are generated. Many clones persist as memory cells, although the clone size is greatly reduced. It would be expected that the large number of cell divisions occurring during clonal expansion would lead to...

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Main Authors: Maini, M, Soares, M, Zilch, C, Akbar, A, Beverley, P
Format: Journal article
Language:English
Published: 1999
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author Maini, M
Soares, M
Zilch, C
Akbar, A
Beverley, P
author_facet Maini, M
Soares, M
Zilch, C
Akbar, A
Beverley, P
author_sort Maini, M
collection OXFORD
description In acute infectious mononucleosis (AIM), very large clones of Ag-specific CD8+ effector T cells are generated. Many clones persist as memory cells, although the clone size is greatly reduced. It would be expected that the large number of cell divisions occurring during clonal expansion would lead to shortening of telomeres, predisposing to replicative senescence. Instead, we show that clonally expanded CD8+ T cells in AIM have paradoxical preservation of telomere length in association with marked up-regulation of telomerase. We postulate that this allows a proportion of responding T cells to enter the memory pool with a preserved capacity to continue dividing so that long-term immunological memory can be maintained.
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spelling oxford-uuid:c992fe93-476d-40da-b8d6-11fd6623ed9a2022-03-27T07:00:14ZVirus-induced CD8+ T cell clonal expansion is associated with telomerase up-regulation and telomere length preservation: a mechanism for rescue from replicative senescence.Journal articlehttp://purl.org/coar/resource_type/c_dcae04bcuuid:c992fe93-476d-40da-b8d6-11fd6623ed9aEnglishSymplectic Elements at Oxford1999Maini, MSoares, MZilch, CAkbar, ABeverley, PIn acute infectious mononucleosis (AIM), very large clones of Ag-specific CD8+ effector T cells are generated. Many clones persist as memory cells, although the clone size is greatly reduced. It would be expected that the large number of cell divisions occurring during clonal expansion would lead to shortening of telomeres, predisposing to replicative senescence. Instead, we show that clonally expanded CD8+ T cells in AIM have paradoxical preservation of telomere length in association with marked up-regulation of telomerase. We postulate that this allows a proportion of responding T cells to enter the memory pool with a preserved capacity to continue dividing so that long-term immunological memory can be maintained.
spellingShingle Maini, M
Soares, M
Zilch, C
Akbar, A
Beverley, P
Virus-induced CD8+ T cell clonal expansion is associated with telomerase up-regulation and telomere length preservation: a mechanism for rescue from replicative senescence.
title Virus-induced CD8+ T cell clonal expansion is associated with telomerase up-regulation and telomere length preservation: a mechanism for rescue from replicative senescence.
title_full Virus-induced CD8+ T cell clonal expansion is associated with telomerase up-regulation and telomere length preservation: a mechanism for rescue from replicative senescence.
title_fullStr Virus-induced CD8+ T cell clonal expansion is associated with telomerase up-regulation and telomere length preservation: a mechanism for rescue from replicative senescence.
title_full_unstemmed Virus-induced CD8+ T cell clonal expansion is associated with telomerase up-regulation and telomere length preservation: a mechanism for rescue from replicative senescence.
title_short Virus-induced CD8+ T cell clonal expansion is associated with telomerase up-regulation and telomere length preservation: a mechanism for rescue from replicative senescence.
title_sort virus induced cd8 t cell clonal expansion is associated with telomerase up regulation and telomere length preservation a mechanism for rescue from replicative senescence
work_keys_str_mv AT mainim virusinducedcd8tcellclonalexpansionisassociatedwithtelomeraseupregulationandtelomerelengthpreservationamechanismforrescuefromreplicativesenescence
AT soaresm virusinducedcd8tcellclonalexpansionisassociatedwithtelomeraseupregulationandtelomerelengthpreservationamechanismforrescuefromreplicativesenescence
AT zilchc virusinducedcd8tcellclonalexpansionisassociatedwithtelomeraseupregulationandtelomerelengthpreservationamechanismforrescuefromreplicativesenescence
AT akbara virusinducedcd8tcellclonalexpansionisassociatedwithtelomeraseupregulationandtelomerelengthpreservationamechanismforrescuefromreplicativesenescence
AT beverleyp virusinducedcd8tcellclonalexpansionisassociatedwithtelomeraseupregulationandtelomerelengthpreservationamechanismforrescuefromreplicativesenescence