This study will analyze cellular and humoral immune responses after seasonal vaccination against influenza. Healthy adults are vaccinated with a licensed trivalent inactivated vaccine without adjuvant. The vaccine is licensed for all age groups studied in this study. MedDRA version: 14.0 Level: LLT Classification code 10016794 Term: Flu vaccination System Organ Class: 10042613 - Surgical and medical procedures MedDRA version: 14.0 Level: LLT Classification code 10046859 Term: Vaccination Syste
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: signed informed consent form participant of the former MARK-AGE study no previous influenza vaccination in the 2011/2012 season Are the trial subjects under 18? no Number of subjects for this age range: F.1.2 Adults (18-64 years) yes F.1.2.1 Number of subjects for this age range 150 F.1.3 Elderly (>=65 years) yes F.1.3.1 Number of subjects for this age range 150
Exclusion criteria
Exclusion criteria: acute illness chronic inflammatory disease (e.g. inflammatory bowl disease, Multiple Sclerosis) chronic infection with HBV, HCV or HIV transplant recipients persons who have recieved chemotherapy in the past persons under immunosuppressive therapy pregnant women participation in another clinical trial during the study
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Main Objective: To analyze the humoral and cellular immune response after influenza vaccination in different age groups (>35 years). Determination of influence of age on vaccine-induced immune response and analysis of interaction between cellular and humoral responses.;Secondary Objective: Identification of biological parameters for prediction of vaccination success. Immunological and biogerontological characterisation of responders and non-responders.;Primary end point(s): Quantification of vaccine-induced immune responses 4 weeks after vaccination | — |
Countries
Austria
Contacts
Institute for Biomedical Aging Research