Measles infection paramyxovirus
Conditions
Interventions
None listed
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: •Previous participation in the study on the immunological effects of early measles vaccination, as described in a separate study protocol (NL45616.094.13/IIV-273) •The parents/legally representatives accept participation in the trial according to the described procedures •Presence of a signed informed consent •Children must have received their NIP vaccinations according to schedule.
Exclusion criteria
Exclusion criteria: •Receiving immunosuppressive medication •Presence of a serious disease that requires medical care that can interfere with the results of the study •Known or suspected immunological disorder •Bleeding disorders
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| • Measles specific serum neutralizing antibodies 6 years after MMR-1 at 14 months of age | — |
Secondary
| Measure | Time frame |
|---|---|
| • Measles specific serum IgG antibody and avidity (Luminex), and functional antibody characteristics prior 6 years after MMR-1 at 14 months of age • Serum IgG antibody concentrations against mumps and rubella (Luminex) 6 years after MMR-1 at 14 months of age • Antibodies against other NIP vaccines 6 years after MMR-1 at 14 months of age | — |
Countries
Netherlands