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T cell memory revisited using single telomere length analysis

Roger, Laureline, Miners, Kelly L., Leonard, Louise, Grimstead, Julia W., Price, David A. ORCID: https://orcid.org/0000-0001-9416-2737, Baird, Duncan M. ORCID: https://orcid.org/0000-0001-8408-5467 and Ladell, Kristin ORCID: https://orcid.org/0000-0002-9856-2938 2023. T cell memory revisited using single telomere length analysis. Frontiers in Immunology 14 , 1100535. 10.3389/fimmu.2023.1100535

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License URL: http://creativecommons.org/licenses/by/4.0/
License Start date: 14 September 2023

Abstract

The fundamental basis of T cell memory remains elusive. It is established that antigen stimulation drives clonal proliferation and differentiation, but the relationship between cellular phenotype, replicative history, and longevity, which is likely essential for durable memory, has proven difficult to elucidate. To address these issues, we used conventional markers of differentiation to identify and isolate various subsets of CD8+ memory T cells and measured telomere lengths in these phenotypically defined populations using the most sensitive technique developed to date, namely single telomere length analysis (STELA). Naive cells were excluded on the basis of dual expression of CCR7 and CD45RA. Memory subsets were sorted as CD27+CD45RA+, CD27intCD45RA+, CD27−CD45RA+, CD27+CD45RAint, CD27−CD45RAint, CD27+CD45RA−, and CD27−CD45RA− at >98% purity. The shortest median telomere lengths were detected among subsets that lacked expression of CD45RA, and the longest median telomere lengths were detected among subsets that expressed CD45RA. Longer median telomere lengths were also a feature of subsets that expressed CD27 in compartments defined by the absence or presence of CD45RA. Collectively, these data suggested a disconnect between replicative history and CD8+ memory T cell differentiation, which is classically thought to be a linear process that culminates with revertant expression of CD45RA.

Item Type: Article
Date Type: Publication
Status: Published
Schools: Medicine
Additional Information: License information from Publisher: LICENSE 1: URL: http://creativecommons.org/licenses/by/4.0/
Publisher: Frontiers Media
ISSN: 1664-3224
Funders: Cancer Research UK, Wellcome Trust
Date of First Compliant Deposit: 29 September 2023
Date of Acceptance: 9 June 2023
Last Modified: 30 Oct 2023 17:40
URI: https://orca.cardiff.ac.uk/id/eprint/162833

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