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Status |
Public on Oct 18, 2016 |
Title |
naive T cell heterogeneity after neonatal thymectomy |
Organism |
Homo sapiens |
Experiment type |
Expression profiling by high throughput sequencing
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Summary |
The generation of new naive T-cells is dependent on thymic output, but in adults the naive T-cell pool is primarily maintained by peripheral proliferation. Naive T-cells have long been regarded as relatively quiescent cells but recently it was shown that IL-8 production is a signatory effector function of naïve T-cells, at least in newborns. With human aging naïve CD4 T-cell numbers decline but it is not clear whether this is accompanied by (functional) differentiation of naïve T-cells and loss of true naivety. Using a unique cohort of children and adolescents who underwent neonatal thymectomy, we demonstrate that the naive CD4 T-cell compartment in healthy humans is functionally heterogeneous and that this functional diversity is lost after neonatal thymectomy. Thymic regeneration later in life resulted in functional restoration of the naïve T-cell compartment. These data shed further light on functional differentiation within the naive T-cell compartment and the importance of the thymus in naive T-cell homeostasis.
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Overall design |
Rna-seq analysis of immune cells derived from healthy controls and thymectomy patients
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Contributor(s) |
Mokry M |
Citation(s) |
26901814 |
Submission date |
Aug 26, 2015 |
Last update date |
May 15, 2019 |
Contact name |
Michal Mokry |
E-mail(s) |
m.mokry@umcutrecht.nl
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Organization name |
Wilhelmina Children's Hospital, University Medical Center Utrecht
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Street address |
Lundlaan 6
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City |
Utrecht |
ZIP/Postal code |
3584 EA |
Country |
Netherlands |
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Platforms (1) |
GPL18573 |
Illumina NextSeq 500 (Homo sapiens) |
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Samples (20)
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Relations |
BioProject |
PRJNA293969 |
SRA |
SRP062865 |