Differential impact of self and environmental antigens on the ontogeny and maintenance of CD4+ T cell memory

Laboratory mice develop populations of circulating memory CD4+ T cells in the absence of overt infection. We have previously shown that these populations are replenished from naive precursors at high levels throughout life (Gossel et al., 2017). However, the nature, relative importance and timing of...

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Main Authors: Thea Hogan, Maria Nowicka, Daniel Cownden, Claire F Pearson, Andrew J Yates, Benedict Seddon
Format: Article
Language:English
Published: eLife Sciences Publications Ltd 2019-11-01
Series:eLife
Subjects:
Online Access:https://elifesciences.org/articles/48901
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spelling doaj-96567a4133f546699da8b9140eb311df2021-05-05T18:06:31ZengeLife Sciences Publications LtdeLife2050-084X2019-11-01810.7554/eLife.48901Differential impact of self and environmental antigens on the ontogeny and maintenance of CD4+ T cell memoryThea Hogan0Maria Nowicka1Daniel Cownden2Claire F Pearson3Andrew J Yates4https://orcid.org/0000-0003-4606-4483Benedict Seddon5https://orcid.org/0000-0003-4352-3373Institute of Immunity and Transplantation, Division of Infection and Immunity, University College London, London, United KingdomDepartment of Pathology and Cell Biology, Columbia University Medical Center, New York, United StatesInstitute of Infection, Immunity and Inflammation, University of Glasgow, Glasgow, United KingdomKennedy Institute of Rheumatology, University of Oxford, Oxford, United KingdomDepartment of Pathology and Cell Biology, Columbia University Medical Center, New York, United StatesInstitute of Immunity and Transplantation, Division of Infection and Immunity, University College London, London, United KingdomLaboratory mice develop populations of circulating memory CD4+ T cells in the absence of overt infection. We have previously shown that these populations are replenished from naive precursors at high levels throughout life (Gossel et al., 2017). However, the nature, relative importance and timing of the forces generating these cells remain unclear. Here, we tracked the generation of memory CD4+ T cell subsets in mice housed in facilities differing in their ‘dirtiness’. We found evidence for sequential naive to central memory to effector memory development, and confirmed that both memory subsets are heterogeneous in their rates of turnover. We also inferred that early exposure to self and environmental antigens establishes persistent memory populations at levels determined largely, although not exclusively, by the dirtiness of the environment. After the first few weeks of life, however, these populations are continuously supplemented by new memory cells at rates that are independent of environment.https://elifesciences.org/articles/48901T cellmemorymicrobiome
collection DOAJ
language English
format Article
sources DOAJ
author Thea Hogan
Maria Nowicka
Daniel Cownden
Claire F Pearson
Andrew J Yates
Benedict Seddon
spellingShingle Thea Hogan
Maria Nowicka
Daniel Cownden
Claire F Pearson
Andrew J Yates
Benedict Seddon
Differential impact of self and environmental antigens on the ontogeny and maintenance of CD4+ T cell memory
eLife
T cell
memory
microbiome
author_facet Thea Hogan
Maria Nowicka
Daniel Cownden
Claire F Pearson
Andrew J Yates
Benedict Seddon
author_sort Thea Hogan
title Differential impact of self and environmental antigens on the ontogeny and maintenance of CD4+ T cell memory
title_short Differential impact of self and environmental antigens on the ontogeny and maintenance of CD4+ T cell memory
title_full Differential impact of self and environmental antigens on the ontogeny and maintenance of CD4+ T cell memory
title_fullStr Differential impact of self and environmental antigens on the ontogeny and maintenance of CD4+ T cell memory
title_full_unstemmed Differential impact of self and environmental antigens on the ontogeny and maintenance of CD4+ T cell memory
title_sort differential impact of self and environmental antigens on the ontogeny and maintenance of cd4+ t cell memory
publisher eLife Sciences Publications Ltd
series eLife
issn 2050-084X
publishDate 2019-11-01
description Laboratory mice develop populations of circulating memory CD4+ T cells in the absence of overt infection. We have previously shown that these populations are replenished from naive precursors at high levels throughout life (Gossel et al., 2017). However, the nature, relative importance and timing of the forces generating these cells remain unclear. Here, we tracked the generation of memory CD4+ T cell subsets in mice housed in facilities differing in their ‘dirtiness’. We found evidence for sequential naive to central memory to effector memory development, and confirmed that both memory subsets are heterogeneous in their rates of turnover. We also inferred that early exposure to self and environmental antigens establishes persistent memory populations at levels determined largely, although not exclusively, by the dirtiness of the environment. After the first few weeks of life, however, these populations are continuously supplemented by new memory cells at rates that are independent of environment.
topic T cell
memory
microbiome
url https://elifesciences.org/articles/48901
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