Evidence map›Paper›PMID 26418064›Full record

ArticlePloS one2015

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

Kalle Kantola, Lea Hedman, Laura Tanner, Ville Simell, Marjaana Mäkinen, Juulia Partanen, Mohammadreza Sadeghi, Riitta Veijola, Mikael Knip, Jorma Ilonen and 5 more

Erratum issuedAbstract read
In one paragraph

Article in PloS one, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

19 citing papers in PubMed.

  1. Review
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  11. Article
  12. Global Distribution of Human Protoparvoviruses.Emerging infectious diseases · 2018
    Article
  13. Article
  14. Human Parvoviruses.Clinical microbiology reviews · 2017
    Review
  15. Article
  16. Correction: Vol. 18, No. 2.Emerging infectious diseases · 2016
    Article
  17. Article
  18. Article
  19. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

15 authors.

Kalle KantolaUniversity of Helsinki, Department of Virology, Helsinki, Finland.
Lea HedmanUniversity of Helsinki, Department of Virology, Helsinki, Finland; Helsinki University Hospital Laboratory Services, Helsinki, Finland.
Laura TannerTurku University Hospital, Department of Pediatrics, Turku, Finland.
Ville SimellMedicity, University of Turku, Turku, Finland.
Marjaana MäkinenMedicity, University of Turku, Turku, Finland.
Juulia PartanenUniversity of Helsinki, Department of Virology, Helsinki, Finland.
Mohammadreza SadeghiUniversity of Helsinki, Department of Virology, Helsinki, Finland.
Riitta VeijolaUniversity of Oulu, Department of Pediatrics, Oulu, Finland.
Mikael KnipUniversity of Helsinki and Helsinki University Hospital, Children's Hospital and Research Programs Unit, Diabetes and Obesity, Helsinki, Finland; Folkhälsan Research Center, Helsinki, Finland; Tampere University Hospital, Tampere Center for Child Health Research, Tampere, Finland.
Jorma IlonenTurku University Hospital, Department of Pediatrics, Turku, Finland; Medicity, University of Turku, Turku, Finland; University of Eastern Finland, Department of Clinical Microbiology, Kuopio, Finland; University of Turku, Immunogenetics Laboratory, Turku, Finland.
Heikki HyötyUniversity of Tampere, Department of Virology, Tampere, Finland.
Jorma ToppariTurku University Hospital, Department of Pediatrics, Turku, Finland; Medicity, University of Turku, Turku, Finland.
Olli SimellMedicity, University of Turku, Turku, Finland.
Klaus HedmanUniversity of Helsinki, Department of Virology, Helsinki, Finland; Helsinki University Hospital Laboratory Services, Helsinki, Finland.
Maria Söderlund-VenermoUniversity of Helsinki, Department of Virology, Helsinki, Finland.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

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.

Indexed as

AdolescentAntibodies, ViralB-LymphocytesChildChild, PreschoolDNA, ViralFemaleFollow-Up StudiesHuman bocavirusHumansImmunoglobulin GImmunoglobulin MInfantMaleParvoviridae InfectionsReal-Time Polymerase Chain ReactionAntibodies, ViralDNA, ViralImmunoglobulin GImmunoglobulin M

Identifiers

PMID26418064
PMCPMC4587975

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.