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Dynamic models of immune responses: what is the ideal level of detail?
BACKGROUND: One of the goals of computational immunology is to facilitate the study of infectious diseases. Dynamic modeling is a powerful tool to integrate empirical data from independent sources, make novel predictions, and to foresee the gaps in the current knowledge. Dynamic models constructed t...
Autores principales: | , , , , |
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Formato: | Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2010
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2933642/ https://www.ncbi.nlm.nih.gov/pubmed/20727155 http://dx.doi.org/10.1186/1742-4682-7-35 |
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author | Thakar, Juilee Poss, Mary Albert, Réka Long, Gráinne H Zhang, Ranran |
author_facet | Thakar, Juilee Poss, Mary Albert, Réka Long, Gráinne H Zhang, Ranran |
author_sort | Thakar, Juilee |
collection | PubMed |
description | BACKGROUND: One of the goals of computational immunology is to facilitate the study of infectious diseases. Dynamic modeling is a powerful tool to integrate empirical data from independent sources, make novel predictions, and to foresee the gaps in the current knowledge. Dynamic models constructed to study the interactions between pathogens and hosts' immune responses have revealed key regulatory processes in the infection. OPTIMUM COMPLEXITY AND DYNAMIC MODELING: We discuss the usability of various deterministic dynamic modeling approaches to study the progression of infectious diseases. The complexity of these models is dependent on the number of components and the temporal resolution in the model. We comment on the specific use of simple and complex models in the study of the progression of infectious diseases. CONCLUSIONS: Models of sub-systems or simplified immune response can be used to hypothesize phenomena of host-pathogen interactions and to estimate rates and parameters. Nevertheless, to study the pathogenesis of an infection we need to develop models describing the dynamics of the immune components involved in the progression of the disease. Incorporation of the large number and variety of immune processes involved in pathogenesis requires tradeoffs in modeling. |
format | Text |
id | pubmed-2933642 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2010 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-29336422010-09-07 Dynamic models of immune responses: what is the ideal level of detail? Thakar, Juilee Poss, Mary Albert, Réka Long, Gráinne H Zhang, Ranran Theor Biol Med Model Commentary BACKGROUND: One of the goals of computational immunology is to facilitate the study of infectious diseases. Dynamic modeling is a powerful tool to integrate empirical data from independent sources, make novel predictions, and to foresee the gaps in the current knowledge. Dynamic models constructed to study the interactions between pathogens and hosts' immune responses have revealed key regulatory processes in the infection. OPTIMUM COMPLEXITY AND DYNAMIC MODELING: We discuss the usability of various deterministic dynamic modeling approaches to study the progression of infectious diseases. The complexity of these models is dependent on the number of components and the temporal resolution in the model. We comment on the specific use of simple and complex models in the study of the progression of infectious diseases. CONCLUSIONS: Models of sub-systems or simplified immune response can be used to hypothesize phenomena of host-pathogen interactions and to estimate rates and parameters. Nevertheless, to study the pathogenesis of an infection we need to develop models describing the dynamics of the immune components involved in the progression of the disease. Incorporation of the large number and variety of immune processes involved in pathogenesis requires tradeoffs in modeling. BioMed Central 2010-08-20 /pmc/articles/PMC2933642/ /pubmed/20727155 http://dx.doi.org/10.1186/1742-4682-7-35 Text en Copyright ©2010 Thakar et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Commentary Thakar, Juilee Poss, Mary Albert, Réka Long, Gráinne H Zhang, Ranran Dynamic models of immune responses: what is the ideal level of detail? |
title | Dynamic models of immune responses: what is the ideal level of detail? |
title_full | Dynamic models of immune responses: what is the ideal level of detail? |
title_fullStr | Dynamic models of immune responses: what is the ideal level of detail? |
title_full_unstemmed | Dynamic models of immune responses: what is the ideal level of detail? |
title_short | Dynamic models of immune responses: what is the ideal level of detail? |
title_sort | dynamic models of immune responses: what is the ideal level of detail? |
topic | Commentary |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2933642/ https://www.ncbi.nlm.nih.gov/pubmed/20727155 http://dx.doi.org/10.1186/1742-4682-7-35 |
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