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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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 |
work_keys_str_mv |
AT theahogan differentialimpactofselfandenvironmentalantigensontheontogenyandmaintenanceofcd4tcellmemory AT marianowicka differentialimpactofselfandenvironmentalantigensontheontogenyandmaintenanceofcd4tcellmemory AT danielcownden differentialimpactofselfandenvironmentalantigensontheontogenyandmaintenanceofcd4tcellmemory AT clairefpearson differentialimpactofselfandenvironmentalantigensontheontogenyandmaintenanceofcd4tcellmemory AT andrewjyates differentialimpactofselfandenvironmentalantigensontheontogenyandmaintenanceofcd4tcellmemory AT benedictseddon differentialimpactofselfandenvironmentalantigensontheontogenyandmaintenanceofcd4tcellmemory |
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1721458759650246656 |