Sequential Versus Simultaneous Pneumococcal Vaccination in Elderly: Immunological Memory and Antibody Levels
- Registration Number
- NCT02637583
- Lead Sponsor
- Jena University Hospital
- Brief Summary
The purpose of the present study is to compare the immunological response of pneumococcal serotype specific B-cells, the humoral immune response and safety after sequential vaccination versus simultaneous vaccination with 13-valent pneumococcal conjugate vaccine (PCV13) and 23-valent polysaccharide vaccine (PPV23) versus single vaccination with PPV23 in a prospective, randomized controlled monocentric head-to head clinical study in elderly. The hypothesis of this study is that simultaneous vaccination with PCV13 and PPV23 might achieve an improved immune-response compared to sequential vaccination or single vaccination.
Adults \>=60 years without previous pneumococcal vaccination will be randomized in three groups and receive either PCV13 on day 0 plus PPV23 6 months later (sequential vaccination) or they receive PCV13 plus PPV23 simultaneous on day 0 (simultaneous vaccination) or they receive PPV23 on day 0 (single vaccination). Blood will be taken for pneumococcal serotype-specific B-memory cells against four vaccine-serotypes (ST), included in PCV13 and PPV23, vaccine-serotype 3 (ST3), vaccine-serotype 14 (ST14), vaccine-serotype 19A (ST19A) and vaccine-serotype 23F (ST23F) at visit 1, 2,4,5,7 and 8 and for antibody levels against the 12 vaccine-serotypes included in PCV13 and PPV23 at visit 1, 3, 4, 6, 7 and 8 in all three groups. Adverse events will be recorded for 28 days after each vaccination.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- All
- Target Recruitment
- 123
- Unvaccinated adults >= 60 years
- Written informed consent
- Hypersensitivity against substances included in both vaccines
- Previous pneumococcal vaccination
- Pneumonia within the last two months
- Active infection
- Autoimmune disease
- Ongoing or planned immunosuppressive therapy (including corticosteroid treatment with prednisolon equivalent dose >= 5 mg/d)
- Active malignant disease
- Drug abuse or alcoholic abuse
- Expectation of life < 2 years
- Coagulation disorders
- Burns or injury on the injection site
- Plegia or paresis of extremity where injection is planned
- Shock
- parallel participation in other clinical trial with intervention
- Infusion of blood products within the last half year
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- PARALLEL
- Arm && Interventions
Group Intervention Description Sequential vaccination PCV13 and PPV23 PPV23 PCV13 0.5 ml intramuscular injection once on day 0 PPV23 0.5 ml intramuscular injection once 6 months later Simultaneous vaccination PCV13 and PPV23 PPV23 PCV13 0.5ml intramuscular injection once on day 0 followed by PPV23 0.5ml intramuscular injection on day 0 Single vaccinationPPV23 PPV23 PPV23 0.5ml intramuscular injection on day 0 Sequential vaccination PCV13 and PPV23 PCV13 PCV13 0.5 ml intramuscular injection once on day 0 PPV23 0.5 ml intramuscular injection once 6 months later Simultaneous vaccination PCV13 and PPV23 PCV13 PCV13 0.5ml intramuscular injection once on day 0 followed by PPV23 0.5ml intramuscular injection on day 0
- Primary Outcome Measures
Name Time Method Immune response of B-memory cells 27-28 weeks after first vaccination Change of immune response of B memory cells against 4 pneumococcal serotypes ST3,ST14,ST19A und ST23F compared to day 0 will be determined by multiparameter flow cytometry. Pneumococcal specific B-cells will be identified by labeling with fluorochrome-coupled polysaccharide antigen, B-memory cells will be identified by expression of characteristic membrane proteins and quantified.
- Secondary Outcome Measures
Name Time Method Humoral immune response 4 weeks, 26 weeks, 30 weeks, 52 weeks, 104 weeks Change of serotype-specific immunoglobulin G concentrations against 12 pneumococcal vaccine-serotypes included in both vaccines PCV13 and PPV23 compared to day 0
Immune response of B-memory cells 1-2 weeks, 26 weeks, 52 weeks, 104 weeks Change immune response of B memory cells against 4 pneumococcal serotypes ST3,ST14,ST19A und ST23F compared to day 0 will be determined by multiparameter flow cytometry. Pneumococcal specific B-cells will be identified by labeling with fluorochrome-coupled polysaccharide antigen, B-memory cells will be identified by expression of characteristic membrane proteins and quantified.
Safety (Adverse events and serious adverse events) 28 days after each vaccination Adverse events and serious adverse events
Trial Locations
- Locations (1)
Center of Infectious Diseases and Infection Control, Jena University Hospital
🇩🇪Jena, Germany