Is immune senescence reversible?

Many genes have been shown to be involved in the decline in immune function of the elderly. However, normal numbers of myeloid and lymphoid colonies can be grown from elderly bone marrow under optimal conditions and some thymic function is preserved well into adult life. It may also be possible to r...

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Main Authors: Beverley, P, Grubeck-Loebenstein, B
Format: Journal article
Language:English
Published: 2000
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author Beverley, P
Grubeck-Loebenstein, B
author_facet Beverley, P
Grubeck-Loebenstein, B
author_sort Beverley, P
collection OXFORD
description Many genes have been shown to be involved in the decline in immune function of the elderly. However, normal numbers of myeloid and lymphoid colonies can be grown from elderly bone marrow under optimal conditions and some thymic function is preserved well into adult life. It may also be possible to reverse partially declining thymic function by IL-7 treatment. Peripheral B and T cells show evidence of dysregulation with production of large clones, changes in subset distribution and altered signalling and cytokine production, particularly decreased IL-2 production in the mouse. The identification of these defects may lead to relatively simple procedures to improve vaccination for the elderly.
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spelling oxford-uuid:2b598c58-4949-4136-b78e-e46563febaf92022-03-26T12:30:19ZIs immune senescence reversible?Journal articlehttp://purl.org/coar/resource_type/c_dcae04bcuuid:2b598c58-4949-4136-b78e-e46563febaf9EnglishSymplectic Elements at Oxford2000Beverley, PGrubeck-Loebenstein, BMany genes have been shown to be involved in the decline in immune function of the elderly. However, normal numbers of myeloid and lymphoid colonies can be grown from elderly bone marrow under optimal conditions and some thymic function is preserved well into adult life. It may also be possible to reverse partially declining thymic function by IL-7 treatment. Peripheral B and T cells show evidence of dysregulation with production of large clones, changes in subset distribution and altered signalling and cytokine production, particularly decreased IL-2 production in the mouse. The identification of these defects may lead to relatively simple procedures to improve vaccination for the elderly.
spellingShingle Beverley, P
Grubeck-Loebenstein, B
Is immune senescence reversible?
title Is immune senescence reversible?
title_full Is immune senescence reversible?
title_fullStr Is immune senescence reversible?
title_full_unstemmed Is immune senescence reversible?
title_short Is immune senescence reversible?
title_sort is immune senescence reversible
work_keys_str_mv AT beverleyp isimmunesenescencereversible
AT grubeckloebensteinb isimmunesenescencereversible