Pertussis
Conditions
Brief summary
This study aims to investigate the effects of aP booster vaccination in children, young adults and elderly on the (long-term) immune response to B. pertussis in three European countries with a different epidemiological background and primary vaccination schedule for pertussis.
Detailed description
The study will be performed in three European countries (UK, Finland and the Netherlands) with a different epidemiological background for pertussis incidence and different age groups will have had different primary schedules with whole cell pertussis (wP) or aP vaccines in their first year of life. Long-term memory responses will be analysed following aP booster vaccination including a detailed assessment of antigen-specific B and T cell responses, serology assays for pertussis antigens and the effect of booster vaccination on dynamic changes in immune cell subsets and gene transcription. There will be four cohorts of healthy volunteers: Cohort A - children aged between 7-10 years Cohort B - children aged between 11-15 years Cohort C - adults aged between 20 to 34 years Cohort D - adults aged between 60-70 years Participants will receive one injection of reduced diphtheria toxoid, tetanus toxoid and reduced acellular pertussis vaccine (dTap)-IPV, (Boostrix® IPV, GlaxoSmithKline (GSK)) combination vaccine intramuscularly in the upper arm. Children (cohorts A and B) will be asked to donate blood four times at different time points, and young and older adults (cohorts C and D) will be asked to donate blood at set time points five times in total over the 12 months duration of the study. The time points will be: * Timepoint 0 - day of vaccination * Timepoint 1 - 1 day after T0 +/- 4 hours * Timepoint 2 - 7 days after T0 +/- 1 day * Timepoint 3 - 14 days after T0 +/- 4 days * Timepoint 4 - 28 days after T0 +/- 4 days * Timepoint 5 - 1 year after T0 +/- 4 weeks
Interventions
BIOLOGICALBoostrix®-IPV combination vaccine
A licensed aP (acellular) booster vaccine developed by GlaxoSmithKline.
Sponsors
National Institute for Public Health and the Environment (RIVM)
University of Turku
University of Oxford
Study design
Allocation
NON_RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
NONE
Eligibility
Sex/Gender
ALL
Age
7 Years to 70 Years
Healthy volunteers
Yes
Inclusion criteria
* Normal general health * Within the right age group for the cohort * Received all regular vaccines for their age group according to the Dutch NIP, UK NIP or Finnish NIP; a copy of the vaccination booklet will be included in the participant's documents. If booklet is not available for cohorts A, B and C, vaccination status will be checked although, for cohort C and D this booklet might not be available due to their age; * Provision of written informed consent * Willing to adhere to the protocol and be available during the study period.
Exclusion criteria
* Present evidence of serious disease(s) within the last 3 months before inclusion requiring immunosuppressive or immune modulating medical treatment, such as systemic corticosteroids, that might interfere with the results of the study; * Chronic infection * Known or suspected immune deficiency; * History of any neurologic disorder, including epilepsy; * Previous administration of serum products (including immunoglobulins) within 6 months before vaccination and blood sampling; * Known and/or suspected allergy to any of the vaccine components (by medical history); * Occurrence of a serious adverse events (SAEs) after primary DTwP-IPV vaccination, DTaP-IPV vaccination or any other vaccination (by medical history); * Vaccination with any other pertussis vaccine other than those described in the inclusion criteria (i.e. only according to NIP) * Vaccination with any other DT-IPV vaccine in the last 5 years, a DT-IPV vaccination according to NIP in cohort B is not an exclusion criterion; * Children between 8 and 10 years of age eligible for cohort A in the Netherlands who have already received the diphtheria and tetanus toxoid vaccine (DT)-IPV booster vaccination according to Dutch NIP around 9 years of age; * Mixed wP and aP priming within a participant, cohort B; * Pregnancy. Detailed considerations for this
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Change from baseline of pertussis toxin-specific IgG antibody levels to 28 days after vaccination | 28 days |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Change from baseline in pertussis toxin (PT) specific IgG-subclasses and avidity levels to 28 days and 1 year after vaccination with Boostrix-IPV | 28 days and 1 year | — |
| Change from baseline of antigen-specific IgG antibody levels against other pertussis vaccine antigens (such as FHA) and non-pertussis vaccine antigens (such as diptheria and tetanus toxoid) to 28 days and 1 year after vaccination with Boostrix-IPV | 28 days and 1 year | — |
| Change from baseline of functional pertussis-specific antibody levels to 28 days and 1 year after vaccination with Boostrix-IPV | 28 days and 1 year | — |
| Amount of pertussis toxin (PT) specific IgG antibody one year after vaccination with Boostrix-IPV | 1 year | — |
| Change from baseline of pertussis antigen-specific T helper responses to 14 days, 28 days and 1 year after vaccination with Boostrix-IPV | 14 days, 28 days and 1 year | To describe the effect on an aP booster on the specific T cell immune response in different age groups that have been initially vaccinated with either a whole cell or acellular vaccine |
| Identify markers in biological samples collected in the Biobank (library of samples) that show changes in immunity to pertussis | 1 year although samples will be stored up to 10 years | Use of novel exploratory immunoassays on stored samples to identify biomarkers or lasting memory or waning immunity to pertussis. |
| Change from baseline of B cell responses against Bordetella pertussis vaccine proteins after vaccination with Boostrix-IPV | 7 days, 28 days and 1 year | Antigen-specific memory B cell responses against B-pertussis vaccine proteins |
Countries
Finland, Netherlands, United Kingdom
Outcome results
None listed