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The Role of Acquired Immunity in the Spread of Human Papillomavirus (HPV): Explorations with a Microsimulation Model

BACKGROUND: Knowledge of the natural history of human papillomavirus (HPV), in particular the role of immunity, is crucial in estimating the (cost-) effectiveness of HPV vaccination and cervical cancer screening strategies, because naturally acquired immunity after clearing an infection may already...

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Autores principales: Matthijsse, Suzette M., van Rosmalen, Joost, Hontelez, Jan A. C., Bakker, Roel, de Kok, Inge M. C. M., van Ballegooijen, Marjolein, de Vlas, Sake J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4314063/
https://www.ncbi.nlm.nih.gov/pubmed/25642941
http://dx.doi.org/10.1371/journal.pone.0116618
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author Matthijsse, Suzette M.
van Rosmalen, Joost
Hontelez, Jan A. C.
Bakker, Roel
de Kok, Inge M. C. M.
van Ballegooijen, Marjolein
de Vlas, Sake J.
author_facet Matthijsse, Suzette M.
van Rosmalen, Joost
Hontelez, Jan A. C.
Bakker, Roel
de Kok, Inge M. C. M.
van Ballegooijen, Marjolein
de Vlas, Sake J.
author_sort Matthijsse, Suzette M.
collection PubMed
description BACKGROUND: Knowledge of the natural history of human papillomavirus (HPV), in particular the role of immunity, is crucial in estimating the (cost-) effectiveness of HPV vaccination and cervical cancer screening strategies, because naturally acquired immunity after clearing an infection may already protect part of the risk population against new HPV infections. METHODS: We used STDSIM, an established stochastic microsimulation model, quantified to the Netherlands. We explored different assumptions regarding the natural history of HPV-16 and HPV-18, and estimated the transmission probabilities and durations of acquired immunity necessary to reproduce age-specific prevalence. RESULTS: A model without acquired immunity cannot reproduce the age-specific patterns of HPV. Also, it is necessary to assume a high degree of individual variation in the duration of infection and acquired immunity. According to the model estimates, on average 20% of women are immune for HPV-16 and 15% for HPV-18. After an HPV-16 infection, 50% are immune for less than 1 year, whereas 20% exceed 30 years. For HPV-18, up to 12% of the individuals are immune for less than 1 year, and about 50% over 30 years. Almost half of all women will never acquire HPV-16 or HPV-18. CONCLUSIONS: Acquired immunity likely plays a major role in HPV epidemiology, but its duration shows substantial variation. Combined with the lifetime risk, this explains to a large extent why many women will never develop cervical cancer.
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spelling pubmed-43140632015-02-13 The Role of Acquired Immunity in the Spread of Human Papillomavirus (HPV): Explorations with a Microsimulation Model Matthijsse, Suzette M. van Rosmalen, Joost Hontelez, Jan A. C. Bakker, Roel de Kok, Inge M. C. M. van Ballegooijen, Marjolein de Vlas, Sake J. PLoS One Research Article BACKGROUND: Knowledge of the natural history of human papillomavirus (HPV), in particular the role of immunity, is crucial in estimating the (cost-) effectiveness of HPV vaccination and cervical cancer screening strategies, because naturally acquired immunity after clearing an infection may already protect part of the risk population against new HPV infections. METHODS: We used STDSIM, an established stochastic microsimulation model, quantified to the Netherlands. We explored different assumptions regarding the natural history of HPV-16 and HPV-18, and estimated the transmission probabilities and durations of acquired immunity necessary to reproduce age-specific prevalence. RESULTS: A model without acquired immunity cannot reproduce the age-specific patterns of HPV. Also, it is necessary to assume a high degree of individual variation in the duration of infection and acquired immunity. According to the model estimates, on average 20% of women are immune for HPV-16 and 15% for HPV-18. After an HPV-16 infection, 50% are immune for less than 1 year, whereas 20% exceed 30 years. For HPV-18, up to 12% of the individuals are immune for less than 1 year, and about 50% over 30 years. Almost half of all women will never acquire HPV-16 or HPV-18. CONCLUSIONS: Acquired immunity likely plays a major role in HPV epidemiology, but its duration shows substantial variation. Combined with the lifetime risk, this explains to a large extent why many women will never develop cervical cancer. Public Library of Science 2015-02-02 /pmc/articles/PMC4314063/ /pubmed/25642941 http://dx.doi.org/10.1371/journal.pone.0116618 Text en © 2015 Matthijsse et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Matthijsse, Suzette M.
van Rosmalen, Joost
Hontelez, Jan A. C.
Bakker, Roel
de Kok, Inge M. C. M.
van Ballegooijen, Marjolein
de Vlas, Sake J.
The Role of Acquired Immunity in the Spread of Human Papillomavirus (HPV): Explorations with a Microsimulation Model
title The Role of Acquired Immunity in the Spread of Human Papillomavirus (HPV): Explorations with a Microsimulation Model
title_full The Role of Acquired Immunity in the Spread of Human Papillomavirus (HPV): Explorations with a Microsimulation Model
title_fullStr The Role of Acquired Immunity in the Spread of Human Papillomavirus (HPV): Explorations with a Microsimulation Model
title_full_unstemmed The Role of Acquired Immunity in the Spread of Human Papillomavirus (HPV): Explorations with a Microsimulation Model
title_short The Role of Acquired Immunity in the Spread of Human Papillomavirus (HPV): Explorations with a Microsimulation Model
title_sort role of acquired immunity in the spread of human papillomavirus (hpv): explorations with a microsimulation model
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4314063/
https://www.ncbi.nlm.nih.gov/pubmed/25642941
http://dx.doi.org/10.1371/journal.pone.0116618
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