A Mechanistic Model for Naive CD4 T Cell Homeostasis in Healthy Adults and Children

The size and composition of the T lymphocyte compartment is subject to strict homeostatic regulation and is remarkably stable throughout life in spite of variable dynamics in cell production and death during T cell development and immune responses. Homeostasis is achieved by careful orchestration of...

Full description

Bibliographic Details
Main Authors: Tharindi eHapuarachchi, Joanna eLewis, Robin eCallard
Format: Article
Language:English
Published: Frontiers Media S.A. 2013-11-01
Series:Frontiers in Immunology
Subjects:
Online Access:http://journal.frontiersin.org/Journal/10.3389/fimmu.2013.00366/full
id doaj-ccd9858644e34138b07ee803d762cc95
record_format Article
spelling doaj-ccd9858644e34138b07ee803d762cc952020-11-24T20:58:41ZengFrontiers Media S.A.Frontiers in Immunology1664-32242013-11-01410.3389/fimmu.2013.0036657110A Mechanistic Model for Naive CD4 T Cell Homeostasis in Healthy Adults and ChildrenTharindi eHapuarachchi0Joanna eLewis1Robin eCallard2University College LondonUniversity College LondonUniversity College LondonThe size and composition of the T lymphocyte compartment is subject to strict homeostatic regulation and is remarkably stable throughout life in spite of variable dynamics in cell production and death during T cell development and immune responses. Homeostasis is achieved by careful orchestration of lymphocyte survival and cell division. New T cells are generated from the thymus and the number of peripheral T cells is regulated by controlling survival and proliferation. How these processes combine is however very complex. Thymic output increases in the first year of life and then decreases but is crucial for establishing repertoire diversity. Proliferation of new naive T-cells plays a crucial role for maintaining numbers but at a potential cost to TCR repertoire diversity. A mechanistic two compartment model of T-cell homeostasis is described here that includes specific terms for thymic output, cell proliferation and cell death of both resting and dividing cells. The model successfully predicts the homeostatic set point for T-cells in adults and identifies variables that determine the total number of T cells. It also accurately predicts T cell numbers in children in early life despite rapid changes in thymic output and growth over this period.http://journal.frontiersin.org/Journal/10.3389/fimmu.2013.00366/fullHomeostasisChildrenmathematical modelingCD4 T cellsmechanistic modellingnaive T cells
collection DOAJ
language English
format Article
sources DOAJ
author Tharindi eHapuarachchi
Joanna eLewis
Robin eCallard
spellingShingle Tharindi eHapuarachchi
Joanna eLewis
Robin eCallard
A Mechanistic Model for Naive CD4 T Cell Homeostasis in Healthy Adults and Children
Frontiers in Immunology
Homeostasis
Children
mathematical modeling
CD4 T cells
mechanistic modelling
naive T cells
author_facet Tharindi eHapuarachchi
Joanna eLewis
Robin eCallard
author_sort Tharindi eHapuarachchi
title A Mechanistic Model for Naive CD4 T Cell Homeostasis in Healthy Adults and Children
title_short A Mechanistic Model for Naive CD4 T Cell Homeostasis in Healthy Adults and Children
title_full A Mechanistic Model for Naive CD4 T Cell Homeostasis in Healthy Adults and Children
title_fullStr A Mechanistic Model for Naive CD4 T Cell Homeostasis in Healthy Adults and Children
title_full_unstemmed A Mechanistic Model for Naive CD4 T Cell Homeostasis in Healthy Adults and Children
title_sort mechanistic model for naive cd4 t cell homeostasis in healthy adults and children
publisher Frontiers Media S.A.
series Frontiers in Immunology
issn 1664-3224
publishDate 2013-11-01
description The size and composition of the T lymphocyte compartment is subject to strict homeostatic regulation and is remarkably stable throughout life in spite of variable dynamics in cell production and death during T cell development and immune responses. Homeostasis is achieved by careful orchestration of lymphocyte survival and cell division. New T cells are generated from the thymus and the number of peripheral T cells is regulated by controlling survival and proliferation. How these processes combine is however very complex. Thymic output increases in the first year of life and then decreases but is crucial for establishing repertoire diversity. Proliferation of new naive T-cells plays a crucial role for maintaining numbers but at a potential cost to TCR repertoire diversity. A mechanistic two compartment model of T-cell homeostasis is described here that includes specific terms for thymic output, cell proliferation and cell death of both resting and dividing cells. The model successfully predicts the homeostatic set point for T-cells in adults and identifies variables that determine the total number of T cells. It also accurately predicts T cell numbers in children in early life despite rapid changes in thymic output and growth over this period.
topic Homeostasis
Children
mathematical modeling
CD4 T cells
mechanistic modelling
naive T cells
url http://journal.frontiersin.org/Journal/10.3389/fimmu.2013.00366/full
work_keys_str_mv AT tharindiehapuarachchi amechanisticmodelfornaivecd4tcellhomeostasisinhealthyadultsandchildren
AT joannaelewis amechanisticmodelfornaivecd4tcellhomeostasisinhealthyadultsandchildren
AT robinecallard amechanisticmodelfornaivecd4tcellhomeostasisinhealthyadultsandchildren
AT tharindiehapuarachchi mechanisticmodelfornaivecd4tcellhomeostasisinhealthyadultsandchildren
AT joannaelewis mechanisticmodelfornaivecd4tcellhomeostasisinhealthyadultsandchildren
AT robinecallard mechanisticmodelfornaivecd4tcellhomeostasisinhealthyadultsandchildren
_version_ 1716785019991621632