Germinal center dynamics during acute and chronic infection

The ability of the immune system to clear pathogens is limited during chronic virus infections where potent long-lived plasma and memory B-cells are produced only after germinal center B-cells undergo many rounds of somatic hypermutations. In this paper, we investigate the mechanisms of germinal cen...

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Main Authors: Samantha Erwin, Stanca M. Ciupe
Format: Article
Language:English
Published: AIMS Press 2017-05-01
Series:Mathematical Biosciences and Engineering
Subjects:
Online Access:https://www.aimspress.com/article/doi/10.3934/mbe.2017037
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author Samantha Erwin
Stanca M. Ciupe
author_facet Samantha Erwin
Stanca M. Ciupe
author_sort Samantha Erwin
collection DOAJ
description The ability of the immune system to clear pathogens is limited during chronic virus infections where potent long-lived plasma and memory B-cells are produced only after germinal center B-cells undergo many rounds of somatic hypermutations. In this paper, we investigate the mechanisms of germinal center B-cell formation by developing mathematical models for the dynamics of B-cell somatic hypermutations. We use the models to determine how B-cell selection and competition for T follicular helper cells and antigen influences the size and composition of germinal centers in acute and chronic infections. We predict that the T follicular helper cells are a limiting resource in driving large numbers of somatic hypermutations and present possible mechanisms that can revert this limitation in the presence of non-mutating and mutating antigen.
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record_format Article
series Mathematical Biosciences and Engineering
spelling doaj-art-a22e5a02c08e4dc6a884f3d739aa71892025-01-24T02:39:47ZengAIMS PressMathematical Biosciences and Engineering1551-00182017-05-0114365567110.3934/mbe.2017037Germinal center dynamics during acute and chronic infectionSamantha Erwin0Stanca M. Ciupe1460 McBryde Hall, Virginia Tech, Blacksburg, VA 24061, USA460 McBryde Hall, Virginia Tech, Blacksburg, VA 24061, USAThe ability of the immune system to clear pathogens is limited during chronic virus infections where potent long-lived plasma and memory B-cells are produced only after germinal center B-cells undergo many rounds of somatic hypermutations. In this paper, we investigate the mechanisms of germinal center B-cell formation by developing mathematical models for the dynamics of B-cell somatic hypermutations. We use the models to determine how B-cell selection and competition for T follicular helper cells and antigen influences the size and composition of germinal centers in acute and chronic infections. We predict that the T follicular helper cells are a limiting resource in driving large numbers of somatic hypermutations and present possible mechanisms that can revert this limitation in the presence of non-mutating and mutating antigen.https://www.aimspress.com/article/doi/10.3934/mbe.2017037b cellstfh cellsgerminal centerssomatic hypermutationsmathematical models
spellingShingle Samantha Erwin
Stanca M. Ciupe
Germinal center dynamics during acute and chronic infection
Mathematical Biosciences and Engineering
b cells
tfh cells
germinal centers
somatic hypermutations
mathematical models
title Germinal center dynamics during acute and chronic infection
title_full Germinal center dynamics during acute and chronic infection
title_fullStr Germinal center dynamics during acute and chronic infection
title_full_unstemmed Germinal center dynamics during acute and chronic infection
title_short Germinal center dynamics during acute and chronic infection
title_sort germinal center dynamics during acute and chronic infection
topic b cells
tfh cells
germinal centers
somatic hypermutations
mathematical models
url https://www.aimspress.com/article/doi/10.3934/mbe.2017037
work_keys_str_mv AT samanthaerwin germinalcenterdynamicsduringacuteandchronicinfection
AT stancamciupe germinalcenterdynamicsduringacuteandchronicinfection