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B-Cell Responses to Human Bocaviruses 1–4: New Insights from a Childhood Follow-Up Study

Human bocaviruses (HBoVs) 1–4 are recently discovered, antigenically similar parvoviruses. We examined the hypothesis that the antigenic similarity of these viruses could give rise to clinically and diagnostically important immunological interactions. IgG and IgM EIAs as well as qPCR were used to st...

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Autores principales: Kantola, Kalle, Hedman, Lea, Tanner, Laura, Simell, Ville, Mäkinen, Marjaana, Partanen, Juulia, Sadeghi, Mohammadreza, Veijola, Riitta, Knip, Mikael, Ilonen, Jorma, Hyöty, Heikki, Toppari, Jorma, Simell, Olli, Hedman, Klaus, Söderlund-Venermo, Maria
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4587975/
https://www.ncbi.nlm.nih.gov/pubmed/26418064
http://dx.doi.org/10.1371/journal.pone.0139096
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author Kantola, Kalle
Hedman, Lea
Tanner, Laura
Simell, Ville
Mäkinen, Marjaana
Partanen, Juulia
Sadeghi, Mohammadreza
Veijola, Riitta
Knip, Mikael
Ilonen, Jorma
Hyöty, Heikki
Toppari, Jorma
Simell, Olli
Hedman, Klaus
Söderlund-Venermo, Maria
author_facet Kantola, Kalle
Hedman, Lea
Tanner, Laura
Simell, Ville
Mäkinen, Marjaana
Partanen, Juulia
Sadeghi, Mohammadreza
Veijola, Riitta
Knip, Mikael
Ilonen, Jorma
Hyöty, Heikki
Toppari, Jorma
Simell, Olli
Hedman, Klaus
Söderlund-Venermo, Maria
author_sort Kantola, Kalle
collection PubMed
description Human bocaviruses (HBoVs) 1–4 are recently discovered, antigenically similar parvoviruses. We examined the hypothesis that the antigenic similarity of these viruses could give rise to clinically and diagnostically important immunological interactions. IgG and IgM EIAs as well as qPCR were used to study ~2000 sera collected from infancy to early adolescence at 3–6-month intervals from 109 children whose symptoms were recorded. We found that HBoV1-4-specific seroprevalences at age 6 years were 80%, 48%, 10%, and 0%, respectively. HBoV1 infections resulted in significantly weaker IgG responses among children who had pre-existing HBoV2 IgG, and vice versa. Furthermore, we documented a complete absence of virus type-specific immune responses in six viremic children who had pre-existing IgG for another bocavirus, indicating that not all HBoV infections can be diagnosed serologically. Our results strongly indicate that interactions between consecutive HBoV infections affect HBoV immunity via a phenomenon called “original antigenic sin”, cross-protection, or both; however, without evident clinical consequences but with important ramifications for the serodiagnosis of HBoV infections. Serological data is likely to underestimate human exposure to these viruses.
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spelling pubmed-45879752015-10-02 B-Cell Responses to Human Bocaviruses 1–4: New Insights from a Childhood Follow-Up Study Kantola, Kalle Hedman, Lea Tanner, Laura Simell, Ville Mäkinen, Marjaana Partanen, Juulia Sadeghi, Mohammadreza Veijola, Riitta Knip, Mikael Ilonen, Jorma Hyöty, Heikki Toppari, Jorma Simell, Olli Hedman, Klaus Söderlund-Venermo, Maria PLoS One Research Article Human bocaviruses (HBoVs) 1–4 are recently discovered, antigenically similar parvoviruses. We examined the hypothesis that the antigenic similarity of these viruses could give rise to clinically and diagnostically important immunological interactions. IgG and IgM EIAs as well as qPCR were used to study ~2000 sera collected from infancy to early adolescence at 3–6-month intervals from 109 children whose symptoms were recorded. We found that HBoV1-4-specific seroprevalences at age 6 years were 80%, 48%, 10%, and 0%, respectively. HBoV1 infections resulted in significantly weaker IgG responses among children who had pre-existing HBoV2 IgG, and vice versa. Furthermore, we documented a complete absence of virus type-specific immune responses in six viremic children who had pre-existing IgG for another bocavirus, indicating that not all HBoV infections can be diagnosed serologically. Our results strongly indicate that interactions between consecutive HBoV infections affect HBoV immunity via a phenomenon called “original antigenic sin”, cross-protection, or both; however, without evident clinical consequences but with important ramifications for the serodiagnosis of HBoV infections. Serological data is likely to underestimate human exposure to these viruses. Public Library of Science 2015-09-29 /pmc/articles/PMC4587975/ /pubmed/26418064 http://dx.doi.org/10.1371/journal.pone.0139096 Text en © 2015 Kantola 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
Kantola, Kalle
Hedman, Lea
Tanner, Laura
Simell, Ville
Mäkinen, Marjaana
Partanen, Juulia
Sadeghi, Mohammadreza
Veijola, Riitta
Knip, Mikael
Ilonen, Jorma
Hyöty, Heikki
Toppari, Jorma
Simell, Olli
Hedman, Klaus
Söderlund-Venermo, Maria
B-Cell Responses to Human Bocaviruses 1–4: New Insights from a Childhood Follow-Up Study
title B-Cell Responses to Human Bocaviruses 1–4: New Insights from a Childhood Follow-Up Study
title_full B-Cell Responses to Human Bocaviruses 1–4: New Insights from a Childhood Follow-Up Study
title_fullStr B-Cell Responses to Human Bocaviruses 1–4: New Insights from a Childhood Follow-Up Study
title_full_unstemmed B-Cell Responses to Human Bocaviruses 1–4: New Insights from a Childhood Follow-Up Study
title_short B-Cell Responses to Human Bocaviruses 1–4: New Insights from a Childhood Follow-Up Study
title_sort b-cell responses to human bocaviruses 1–4: new insights from a childhood follow-up study
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4587975/
https://www.ncbi.nlm.nih.gov/pubmed/26418064
http://dx.doi.org/10.1371/journal.pone.0139096
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