Tracing thymic output in older individuals.

Details

Serval ID
serval:BIB_829FA73D7FE1
Type
Article: article from journal or magazin.
Collection
Publications
Title
Tracing thymic output in older individuals.
Journal
Clinical and Experimental Immunology
Author(s)
Mitchell W.A., Lang P.O., Aspinall R.
ISSN
1365-2249 (Electronic)
ISSN-L
0009-9104
Publication state
Published
Issued date
2010
Peer-reviewed
Oui
Volume
161
Number
3
Pages
497-503
Language
english
Notes
Publication types: Journal Article ; Multicenter Study ; Research Support, Non-U.S. Gov'tPublication Status: ppublish
Abstract
As a result of age-associated thymic atrophy, T cell production declines with age. Some studies suggest that production undergoes an exponential decline starting at birth, while others consider the decline to be in a biphasic manner with a rapid reduction in output occurring before middle age followed by a phase in which output declines at a regular, albeit much slower, rate. Both approaches provide estimations of the time of termination of thymic output, but on the basis of limited amounts of data. We have analysed blood from more than 200 individuals between the ages of 58 and 104 years to determine changes in thymic output using signal-joint T cell receptor excision circles (sjTREC)/T cells as our measure. To reduce any potential geographical or nutritional bias we have obtained samples from five different European countries. Our results reveal that while the absolute number of T cells per microlitre of blood does not change significantly across the age range we tested, the values of sjTREC per microlitre show wide variation and reveal an age-associated decline in thymic output. In addition we show gender differences, with notably higher thymic output in females than males at each decade. More importantly, we noted a significant decline in sjTREC/T cell levels in those more than 90 years of age in both males and females. Our results provide information about the potential end-point for thymic output and suggest that sjTREC analysis may be a biomarker of effective ageing.
Keywords
Aged, Aging, Antigens, CD3/metabolism, Female, Gene Expression Regulation, Developmental, Gene Rearrangement, T-Lymphocyte/genetics, Humans, Leukocyte Count, Lymphocyte Count, Male, Middle Aged, Receptors, Antigen, T-Cell/genetics, Receptors, Antigen, T-Cell/metabolism, Reverse Transcriptase Polymerase Chain Reaction, T-Lymphocytes/metabolism, Thymus Gland/growth & development, Thymus Gland/metabolism
Pubmed
Open Access
Yes
Create date
15/04/2015 9:26
Last modification date
20/08/2019 15:42
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