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The Timing of T Cell Priming and Cycling

The proliferation of specific lymphocytes is the central tenet of the clonal selection paradigm. Antigen recognition by T cells triggers a series of events that produces expanded clones of differentiated effector cells. TCR signaling events are detectable within seconds and minutes and are likely to...

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Autor principal: Obst, Reinhard
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4633513/
https://www.ncbi.nlm.nih.gov/pubmed/26594213
http://dx.doi.org/10.3389/fimmu.2015.00563
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author Obst, Reinhard
author_facet Obst, Reinhard
author_sort Obst, Reinhard
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description The proliferation of specific lymphocytes is the central tenet of the clonal selection paradigm. Antigen recognition by T cells triggers a series of events that produces expanded clones of differentiated effector cells. TCR signaling events are detectable within seconds and minutes and are likely to continue for hours and days in vivo. Here, I review the work done on the importance of TCR signals in the later part of the expansion phase of the primary T cell response, primarily regarding the regulation of the cell cycle in CD4(+) and CD8(+) cells. The results suggest a degree of programing by early signals for effector differentiation, particularly in the CD8(+) T cell compartment, with optimal expansion supported by persistent antigen presentation later on. Differences to CD4(+) T cell expansion and new avenues toward a molecular understanding of cell cycle regulation in lymphocytes are discussed.
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spelling pubmed-46335132015-11-20 The Timing of T Cell Priming and Cycling Obst, Reinhard Front Immunol Immunology The proliferation of specific lymphocytes is the central tenet of the clonal selection paradigm. Antigen recognition by T cells triggers a series of events that produces expanded clones of differentiated effector cells. TCR signaling events are detectable within seconds and minutes and are likely to continue for hours and days in vivo. Here, I review the work done on the importance of TCR signals in the later part of the expansion phase of the primary T cell response, primarily regarding the regulation of the cell cycle in CD4(+) and CD8(+) cells. The results suggest a degree of programing by early signals for effector differentiation, particularly in the CD8(+) T cell compartment, with optimal expansion supported by persistent antigen presentation later on. Differences to CD4(+) T cell expansion and new avenues toward a molecular understanding of cell cycle regulation in lymphocytes are discussed. Frontiers Media S.A. 2015-11-05 /pmc/articles/PMC4633513/ /pubmed/26594213 http://dx.doi.org/10.3389/fimmu.2015.00563 Text en Copyright © 2015 Obst. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Immunology
Obst, Reinhard
The Timing of T Cell Priming and Cycling
title The Timing of T Cell Priming and Cycling
title_full The Timing of T Cell Priming and Cycling
title_fullStr The Timing of T Cell Priming and Cycling
title_full_unstemmed The Timing of T Cell Priming and Cycling
title_short The Timing of T Cell Priming and Cycling
title_sort timing of t cell priming and cycling
topic Immunology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4633513/
https://www.ncbi.nlm.nih.gov/pubmed/26594213
http://dx.doi.org/10.3389/fimmu.2015.00563
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