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Exclusion of circulating T cells from the thymus does not apply in the neonatal period
Although T cells arise in the thymus, migration of mature postthymic T cells back to the thymus is very limited in adult mice and is restricted to activated cells. In neonates, by contrast, we present evidence that circulating CD4+ and CD8+ T cells with a naive/resting phenotype readily enter the th...
Formato: | Texto |
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Lenguaje: | English |
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The Rockefeller University Press
1993
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2190888/ https://www.ncbi.nlm.nih.gov/pubmed/8426109 |
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collection | PubMed |
description | Although T cells arise in the thymus, migration of mature postthymic T cells back to the thymus is very limited in adult mice and is restricted to activated cells. In neonates, by contrast, we present evidence that circulating CD4+ and CD8+ T cells with a naive/resting phenotype readily enter the thymus after intravenous injection and remain there for prolonged periods. The migration of resting T cells to the neonatal thymus is largely limited to an unusual subset of cells which lacks expression of the lymph node homing receptor, leukocyte- endothelial cell adhesion molecule 1 (LECAM-1) (MEL-14). Migration of mature T cells to the thymus in neonates may be important for self- tolerance induction. |
format | Text |
id | pubmed-2190888 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 1993 |
publisher | The Rockefeller University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-21908882008-04-16 Exclusion of circulating T cells from the thymus does not apply in the neonatal period J Exp Med Articles Although T cells arise in the thymus, migration of mature postthymic T cells back to the thymus is very limited in adult mice and is restricted to activated cells. In neonates, by contrast, we present evidence that circulating CD4+ and CD8+ T cells with a naive/resting phenotype readily enter the thymus after intravenous injection and remain there for prolonged periods. The migration of resting T cells to the neonatal thymus is largely limited to an unusual subset of cells which lacks expression of the lymph node homing receptor, leukocyte- endothelial cell adhesion molecule 1 (LECAM-1) (MEL-14). Migration of mature T cells to the thymus in neonates may be important for self- tolerance induction. The Rockefeller University Press 1993-02-01 /pmc/articles/PMC2190888/ /pubmed/8426109 Text en This article is distributed under the terms of an Attribution–Noncommercial–Share Alike–No Mirror Sites license for the first six months after the publication date (see http://www.rupress.org/terms). After six months it is available under a Creative Commons License (Attribution–Noncommercial–Share Alike 4.0 Unported license, as described at http://creativecommons.org/licenses/by-nc-sa/4.0/). |
spellingShingle | Articles Exclusion of circulating T cells from the thymus does not apply in the neonatal period |
title | Exclusion of circulating T cells from the thymus does not apply in the neonatal period |
title_full | Exclusion of circulating T cells from the thymus does not apply in the neonatal period |
title_fullStr | Exclusion of circulating T cells from the thymus does not apply in the neonatal period |
title_full_unstemmed | Exclusion of circulating T cells from the thymus does not apply in the neonatal period |
title_short | Exclusion of circulating T cells from the thymus does not apply in the neonatal period |
title_sort | exclusion of circulating t cells from the thymus does not apply in the neonatal period |
topic | Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2190888/ https://www.ncbi.nlm.nih.gov/pubmed/8426109 |