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Model structure analysis to estimate basic immunological processes and maternal risk for parvovirus B19
After a steep monotone rise with age, the seroprevalence profiles for human parvovirus B19 (PVB19) display a decrease or plateau between the ages of 20 and 40, in each of 5 European countries. We investigate whether this phenomenon is induced by waning antibodies for PVB19 and, if this is the case,...
Autores principales: | , , , |
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Formato: | Texto |
Lenguaje: | English |
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Oxford University Press
2011
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3062149/ https://www.ncbi.nlm.nih.gov/pubmed/20841333 http://dx.doi.org/10.1093/biostatistics/kxq059 |
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author | Goeyvaerts, Nele Hens, Niel Aerts, Marc Beutels, Philippe |
author_facet | Goeyvaerts, Nele Hens, Niel Aerts, Marc Beutels, Philippe |
author_sort | Goeyvaerts, Nele |
collection | PubMed |
description | After a steep monotone rise with age, the seroprevalence profiles for human parvovirus B19 (PVB19) display a decrease or plateau between the ages of 20 and 40, in each of 5 European countries. We investigate whether this phenomenon is induced by waning antibodies for PVB19 and, if this is the case, whether secondary infections are plausible, or whether boosting may occur. Several immunological scenarios are tested for PVB19 by fitting different compartmental dynamic transmission models to serological data using data on social contact patterns. The social contact approach has already been shown informative to estimate transmission rates and the basic reproduction number for infections transmitted predominantly through nonsexual social contacts. Our results show that for 4 countries, model selection criteria favor the scenarios allowing for waning immunity at an age-specific rate over the assumption of lifelong immunity, assuming that the transmission rates are directly proportional to the contact rates. Different views on the evolution of the immune response to PVB19 infection lead to altered estimates of the age-specific force of infection and the basic reproduction number. The scenarios which allow for multiple infections during one lifetime predict a higher frequency of PVB19 infection in pregnant women and of associated fetal deaths. When prevaccination serological data are available, the framework developed in this paper could prove worthwhile to investigate these different scenarios for other infections as well, such as cytomegalovirus. |
format | Text |
id | pubmed-3062149 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-30621492011-03-23 Model structure analysis to estimate basic immunological processes and maternal risk for parvovirus B19 Goeyvaerts, Nele Hens, Niel Aerts, Marc Beutels, Philippe Biostatistics Articles After a steep monotone rise with age, the seroprevalence profiles for human parvovirus B19 (PVB19) display a decrease or plateau between the ages of 20 and 40, in each of 5 European countries. We investigate whether this phenomenon is induced by waning antibodies for PVB19 and, if this is the case, whether secondary infections are plausible, or whether boosting may occur. Several immunological scenarios are tested for PVB19 by fitting different compartmental dynamic transmission models to serological data using data on social contact patterns. The social contact approach has already been shown informative to estimate transmission rates and the basic reproduction number for infections transmitted predominantly through nonsexual social contacts. Our results show that for 4 countries, model selection criteria favor the scenarios allowing for waning immunity at an age-specific rate over the assumption of lifelong immunity, assuming that the transmission rates are directly proportional to the contact rates. Different views on the evolution of the immune response to PVB19 infection lead to altered estimates of the age-specific force of infection and the basic reproduction number. The scenarios which allow for multiple infections during one lifetime predict a higher frequency of PVB19 infection in pregnant women and of associated fetal deaths. When prevaccination serological data are available, the framework developed in this paper could prove worthwhile to investigate these different scenarios for other infections as well, such as cytomegalovirus. Oxford University Press 2011-04 2010-09-14 /pmc/articles/PMC3062149/ /pubmed/20841333 http://dx.doi.org/10.1093/biostatistics/kxq059 Text en © 2010 The Author(s) This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/2.5), which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Articles Goeyvaerts, Nele Hens, Niel Aerts, Marc Beutels, Philippe Model structure analysis to estimate basic immunological processes and maternal risk for parvovirus B19 |
title | Model structure analysis to estimate basic immunological processes and maternal risk for parvovirus B19 |
title_full | Model structure analysis to estimate basic immunological processes and maternal risk for parvovirus B19 |
title_fullStr | Model structure analysis to estimate basic immunological processes and maternal risk for parvovirus B19 |
title_full_unstemmed | Model structure analysis to estimate basic immunological processes and maternal risk for parvovirus B19 |
title_short | Model structure analysis to estimate basic immunological processes and maternal risk for parvovirus B19 |
title_sort | model structure analysis to estimate basic immunological processes and maternal risk for parvovirus b19 |
topic | Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3062149/ https://www.ncbi.nlm.nih.gov/pubmed/20841333 http://dx.doi.org/10.1093/biostatistics/kxq059 |
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