IgG Seroreactivites to Viral Capsid Protein VP1 of JC and BK Polyomaviruses in Children at Early Ages with Special Reference to Parental Cofactors

Author:

Laine Hanna K.12,Waterboer Tim3,Syrjänen Kari4,Grenman Seija5,Louvanto Karolina67ORCID,Syrjänen Stina28ORCID

Affiliation:

1. Department of Oral and Maxillofacial Diseases, University of Helsinki, 00290 Helsinki, Finland

2. Department of Oral Pathology and Radiology, Faculty of Medicine, University of Turku, 20520 Turku, Finland

3. Division of Infections and Cancer Epidemiology, German Cancer Research Center (DKFZ), 69120 Heidelberg, Germany

4. SMW Consultants, Ltd., 21620 Kaarina, Finland

5. Department of Obstetrics and Gynecology, University of Turku, Turku University Hospital, 20014 Turku, Finland

6. Department of Obstetrics and Gynecology, Faculty of Medicine and Health Technology, Tampere University, 33520 Tampere, Finland

7. Department of Obstetrics and Gynecology, Tampere University Hospital, 33100 Tampere, Finland

8. Department of Pathology, University of Turku, Turku University Hospital, 20520 Turku, Finland

Abstract

BK (BKPyV) and JC (JCPyV) polyomaviruses are widespread in humans. Transmission at an early age and the role of parents in spreading these viruses through the family are incompletely understood. Our aim was to determine the seroprevalence of BKPyV and JCPyV in infants at the age of 1, 2, 6, 12, 24, and 36 months and to assess the frequency of BKPyV and JCPyV seroconversion. A variety of maternal and paternal covariates were also tested as potential predictors of these early childhood infections. We used multiplex serology to analyze antibodies to BKPyV and JCPyV from baseline to 3-year follow-up visits. We observed that there was nearly perfect correlation in BKPyV and JCPyV serum IgG antibody levels between the mother-infant pairs during the first year of the infant’s life. No correlation among BKPyV antibody titers were found in father–child pairs, whereas JCPyV antibody levels of the father and child had a significant correlation at the 2-year follow-up visit. BKPyV infection may be associated with a child’s predisposition to allergy. In conclusion, after the decay of maternal antibodies, children start to develop their own immunity toward BKPyV and JCPyV, and horizontal transmission of infection in the family can occur.

Publisher

MDPI AG

Subject

Pediatrics, Perinatology and Child Health

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