Developing a First-void Urine-based Infection Model to Study HPV-specific Antibody-virion Interaction Before and After Vaccination With the Gardasil-9 HPV Vaccine - a Non-randomized Open-label Study.
Overview
- Phase
- Phase 2
- Status
- Not yet recruiting
- Sponsor
- Universiteit Antwerpen
- Enrollment
- 50
- Locations
- 3
- Primary Endpoint
- Detection of HPV16 E1^E4 spliced mRNA in an in vitro infection model using first-void urine samples
Overview
Brief Summary
The current study is an open-label, non-randomized, longitudinal exploratory trial using the licensed Gardasil 9 (9vHPV) vaccine in an off-label context to investigate biological and immunological outcomes in human papillomavirus type 16 (HPV16) positive women. Two doses of the licensed Gardasil 9 vaccine will be administered to approximately 50 women between 18 and 45 years old, who test positive for HPV16 DNA at baseline using a type-specific quantitative PCR assay, but have no presence of apparent anogenital lesions and are thus not referred for treatment or intervention at the time of inclusion.
The primary objective of this study is to demonstrate that vaccination with a two-dose regimen of the 9vHPV vaccine reduces the viral infectivity of particles in the female genital tract of HPV16-positive women, by using first-void urine samples. The secondary objectives are to follow up HPV type-specific antibody responses in these first-void urine samples after natural infection and vaccination after one or two doses of the 9vHPV vaccine and to compare these with the responses in serum, and to monitor HPV infections in first-void urine over time.
Candidates will be selected for participation based on the result of their HPV DNA test performed on a sample collected during routine screening or symptomatic (opportunistic) testing in one of the following centers:
- The University Hospital of Antwerp (UZA).
- The University Hospital of Leuven (UZ Leuven).
- Ghent University Hospital (UZ Gent).
Women are followed for up to 24 months, in which first-void urine and serum samples will be collected at different timepoints.
The following laboratory procedures will be applied to reach study objectives
- Assessment of HPV DNA positivity: HPV genotyping in first-void urine samples.
- Assessment of HPV infectivity: Detection of HPV16 E1^E4 spliced mRNA in HaCaT keratinocytes after infection with virions from first-void urine samples.
- Assessment of HPV immunogenicity: Detection of HPV-specific antibodies in first-void urine and serum samples.
Study Design
- Study Type
- Interventional
- Allocation
- Na
- Intervention Model
- Single Group
- Primary Purpose
- Prevention
- Masking
- None
Eligibility Criteria
- Ages
- 18 Years to 45 Years (Adult)
- Sex
- Female
- Accepts Healthy Volunteers
- No
Inclusion Criteria
- •Candidates are eligible for inclusion in the study if they:
- •Are females between 18 and 45 years old (including both limits) at the time of signing the informed consent form.
- •Have tested positive for HPV16 DNA (single or co-infection) but have no presence of apparent anogenital lesions and are thus not referred for treatment or intervention at the time of inclusion or within the last twelve months before inclusion.
- •Did not receive prior vaccination with a prophylactic HPV vaccine.
- •Are able to understand the information brochure and what the study is about.
- •Are willing to give informed consent to the study team to access their medical records, including details on their HPV vaccination schedule and cervical cancer screening results (smears, HPV tests, colposcopy, biopsy).
- •Candidates must be excluded from the study if they:
- •Are previously (completely or partially) vaccinated against HPV or have planned administration of another HPV vaccine during the study.
- •Are pregnant at the time of signing informed consent or are planning to become pregnant within the full duration of the study. Participants must use an effective method of contraception throughout the entire study. Acceptable methods include combined hormonal contraception (oral, vaginal ring, transdermal patch), progestogen-only contraception (oral, injectable, implantable), intrauterine device (IUD)/intrauterine system (IUS), condom, vasectomized male partner, or (periodic) abstinence. Lactating women may be included.
- •Have had full hysterectomy.
Exclusion Criteria
- Not provided
Arms & Interventions
Gardasil 9 Vaccination
Single arm
Intervention: Gardasil 9 (2 dose regimen) (Biological)
Outcomes
Primary Outcomes
Detection of HPV16 E1^E4 spliced mRNA in an in vitro infection model using first-void urine samples
Time Frame: 24 months
Presence and relative expression level of HPV16 E1\^E4 spliced mRNA in HaCaT keratinocytes following in vitro infection with HPV virions isolated from first-void urine samples collected before and after administration of two doses of the Gardasil 9 vaccine.
Secondary Outcomes
- Detection of HPV type-specific antibodies in first-void urine and serum samples(24 months)
- Detection of HPV DNA in first-void urine samples(24 months)
Investigators
Wiebren Tjalma
Prof. Dr. Wiebren A.A Tjalma
Universiteit Antwerpen