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Investigating the Dynamics of MCMV-Specific CD8(+) T Cell Responses in Individual Hosts

Infection by Cytomegalovirus (CMV) is characterized by the massive expansion and continued maintenance of CMV-specific CD8(+) T cells for certain CMV-derived peptides. This phenomenon called “memory inflation" has made CMV a primary target for the generation of T cell based vaccine vectors agai...

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Autores principales: Gabel, Michael, Baumann, Nicolas S., Oxenius, Annette, Graw, Frederik
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6595046/
https://www.ncbi.nlm.nih.gov/pubmed/31281313
http://dx.doi.org/10.3389/fimmu.2019.01358
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author Gabel, Michael
Baumann, Nicolas S.
Oxenius, Annette
Graw, Frederik
author_facet Gabel, Michael
Baumann, Nicolas S.
Oxenius, Annette
Graw, Frederik
author_sort Gabel, Michael
collection PubMed
description Infection by Cytomegalovirus (CMV) is characterized by the massive expansion and continued maintenance of CMV-specific CD8(+) T cells for certain CMV-derived peptides. This phenomenon called “memory inflation" has made CMV a primary target for the generation of T cell based vaccine vectors against various diseases. However, many aspects concerning the generation and maintenance of the inflationary CD8(+) T cell response still remain to be resolved. In this study, we combined experimental data and mathematical models to analyze the dynamics of circulatory inflationary CD8(+) T cells within individual mice infected by MCMV. Obtaining frequent measurements on the number and frequency of CMV-specific CD8(+) T cells up to 70 days post infection, we find that mathematical models assuming differing viral stimuli during acute infection and the inflationary phase provide a better description for the observed dynamics than models relying on similar viral stimuli during both phases. In addition, our analysis allowed a detailed quantification of the different phases of memory inflation within individual mice (1(st)-expansion - contraction - 2(nd) expansion/maintenance) indicating remarkable consistency of the timing of these phases across mice, but considerable variation in the size of the individual responses between mice. Our analysis provides a first step toward generating a mechanistic framework for analyzing the generation and maintenance of inflationary CD8(+) T cells while accounting for individual heterogeneity. Extending these analyses by incorporating measurements from additional compartments and more prolonged sampling will help to obtain a systematic and quantitative understanding of the factors regulating the process of memory inflation.
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spelling pubmed-65950462019-07-05 Investigating the Dynamics of MCMV-Specific CD8(+) T Cell Responses in Individual Hosts Gabel, Michael Baumann, Nicolas S. Oxenius, Annette Graw, Frederik Front Immunol Immunology Infection by Cytomegalovirus (CMV) is characterized by the massive expansion and continued maintenance of CMV-specific CD8(+) T cells for certain CMV-derived peptides. This phenomenon called “memory inflation" has made CMV a primary target for the generation of T cell based vaccine vectors against various diseases. However, many aspects concerning the generation and maintenance of the inflationary CD8(+) T cell response still remain to be resolved. In this study, we combined experimental data and mathematical models to analyze the dynamics of circulatory inflationary CD8(+) T cells within individual mice infected by MCMV. Obtaining frequent measurements on the number and frequency of CMV-specific CD8(+) T cells up to 70 days post infection, we find that mathematical models assuming differing viral stimuli during acute infection and the inflationary phase provide a better description for the observed dynamics than models relying on similar viral stimuli during both phases. In addition, our analysis allowed a detailed quantification of the different phases of memory inflation within individual mice (1(st)-expansion - contraction - 2(nd) expansion/maintenance) indicating remarkable consistency of the timing of these phases across mice, but considerable variation in the size of the individual responses between mice. Our analysis provides a first step toward generating a mechanistic framework for analyzing the generation and maintenance of inflationary CD8(+) T cells while accounting for individual heterogeneity. Extending these analyses by incorporating measurements from additional compartments and more prolonged sampling will help to obtain a systematic and quantitative understanding of the factors regulating the process of memory inflation. Frontiers Media S.A. 2019-06-19 /pmc/articles/PMC6595046/ /pubmed/31281313 http://dx.doi.org/10.3389/fimmu.2019.01358 Text en Copyright © 2019 Gabel, Baumann, Oxenius and Graw. 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) and the copyright owner(s) 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
Gabel, Michael
Baumann, Nicolas S.
Oxenius, Annette
Graw, Frederik
Investigating the Dynamics of MCMV-Specific CD8(+) T Cell Responses in Individual Hosts
title Investigating the Dynamics of MCMV-Specific CD8(+) T Cell Responses in Individual Hosts
title_full Investigating the Dynamics of MCMV-Specific CD8(+) T Cell Responses in Individual Hosts
title_fullStr Investigating the Dynamics of MCMV-Specific CD8(+) T Cell Responses in Individual Hosts
title_full_unstemmed Investigating the Dynamics of MCMV-Specific CD8(+) T Cell Responses in Individual Hosts
title_short Investigating the Dynamics of MCMV-Specific CD8(+) T Cell Responses in Individual Hosts
title_sort investigating the dynamics of mcmv-specific cd8(+) t cell responses in individual hosts
topic Immunology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6595046/
https://www.ncbi.nlm.nih.gov/pubmed/31281313
http://dx.doi.org/10.3389/fimmu.2019.01358
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