human papillomavirus, immune response, vaccination
Conditions
Interventions
bivalent HPV vaccination
Sponsors
RIVM
Eligibility
Age
12 Years to 64 Years
Inclusion criteria
Inclusion criteria: female born in 1993/1994/2001 eligible for national HPV vaccination in 2009/2010/2014
Exclusion criteria
Exclusion criteria: pregnant vaccinated against HPV (only for birth cohorts in 1993/1994)
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| The main study parameters are: - hrHPV DNA types 16/18 in vaginal self-sample - Viral load in vaginal self-samples that are positive for HPV DNA type 16/18 - hrHPV-type specific antibody levels against HPV types 16/18 in serum | — |
Secondary
| Measure | Time frame |
|---|---|
| Further objectives are to obtain insight into the immune mechanism and presence of other HPV DNA types and antibodies against other HPV types: - Level of HPV16/18 and possibly also other high risk HPV type specific immune cells, like T- and B-cells in blood - HPV-16/18 IgG and possibly IgA antibodies present in serum and vaginal secretion - Antibody levels against non-HPV16/18 types in serum and vaginal secretion - Non-HPV 16/18 DNA types in vaginal self-sample - Methylation of tumor suppressor genes, such as CADM1 and MAL for HPV 16/18 and for other hrHPV types - HPV (L1, whole genome) sequence diversity between girls. - Immune parameters ? Microbiota and mycobiota status | — |
Countries
Netherlands
Contacts
Public ContactH.E. de Melker
RIVM
Outcome results
None listed