Polio, Vaccine Reaction
Conditions
Keywords
Immunogenicity, Antibody persistence, Safety, Sabin IPV, bOPV
Brief summary
This study is to evaluate the immunogenicity and safety of Sabin IPV or bOPV, given as a booster vaccination in children aged 4 years who were previously immunised with different sequential immunization history by Sabin IPV and bOPV, and to observe the antibody persistence three years after different primary sequential immunization with Sabin IPV or bOPV at age 2, 3 and 4 months.
Detailed description
This is a continuous study of preliminary trial (Immunogenicity of three sequential schedules with Sabin inactivated poliovirus vaccine and bivalent oral poliovirus vaccine in Zhejiang, China: NCT03147560) . The investigators will follow up previous participants at age 4 years old with different primary sequential immunization schedules at age 2, 3 and 4 months: sIPV-bOPV-bOPV , sIPV-sIPV-bOPV , or sIPV-sIPV-sIPV, and give the 4th doses of polio vaccine with Sabin IPV or bOPV. A pre-vaccination blood sample is taken for polio antibody determinations. Sabin IPV will be administrated for participants in the previous Group 1 (sIPV-bOPV-bOPV), and Sabin IPV or bOPV will be given for participants in the previous Group 2 (sIPV-sIPV-bOPV) and Group 3 (sIPV-sIPV-sIPV) after they were randomly divided into two subgroups. At least two active surveillance visits, during which staff visited the participants s at home (on days 3 and 30) will required after vaccination to collect adverse reaction data. Parents or legal guardians were instructed to contact investigators if they observed any possible vaccine-related adverse events or important medical events (such as serious illness, physical disability, or death). The second blood sample will be collected 28-60 days after the booster vaccination. The investigators will asess the immunogenicity by seroconversion rate and seropositivity after the booster vaccination, and evaluate the antibody persistence using seropositive rate and GMT in participants before the booster vaccination. Safety will assessed with the occurrence of adverse events reported across the study groups.
Interventions
BIOLOGICALvaccinated with Sabin IPV
the 4th dose of polio vaccination
BIOLOGICALvaccinated with bOPV
the 4th dose of polio vaccination
Sponsors
China National Biotec Group Company ltd
Zhejiang Provincial Center for Disease Control and Prevention
Study design
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
NONE
Eligibility
Sex/Gender
ALL
Age
48 Months to 51 Months
Healthy volunteers
Yes
Inclusion criteria
* Participants aged ≥48 months to ≤ 51 months from preliminary study (NCT03147560) with sequential immunization history by Sabin IPV and bOPV. * Parent/legal acceptable representative is willing and able to understand the protocol requirements and provide informed consent. * ≥ 14 days interval between the last vaccination. * Body temperature ≤ 37.2℃.
Exclusion criteria
* Known acute illness, severe chronic disease, acute exacerbation of chronic disease and fever. * Known allergy to any constituent of the vaccine. * Had 4 doses vaccination record of polio vaccine. * Known impairment of immunologic function, or receipt of immunosuppressive therapy or immunoglobulin . * Received non-specific immunoglobulin within 1 month. * An acute illness with fever (temperature ≥ 37.3℃) or any infectious diseases. * Patients with a well-diagnosed history of thrombocytopenia or other coagulation disorders that may cause contraindications for injection. * Any condition which, in the opinion of the investigator, would pose a health risk to the subject or interfere with the vaccine.
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Seroconversion rates of the booster vaccination | before and 28-60 days after the booster dose (4 years old) of polio vaccine | Defined as any positive antibody (titre ≥ 8) response in children who were seronegative prior to the vaccination, or at least a fourfold increase in type-specific antibody levels for children who had pre-existing positive antibodies |
| Persistence (tite rates) of antibodies against poliovirus 3 years after the primary 3 dose polio vaccine immunization | 3 years after the primary three doses of polio immunization(before the booster vaccination ) | The percentage of participants with positive antibody(titre ≥ 8) against all three serotypes of poliovirus 3 years after the primary immunization with different sequential immunization schedules using sIPV or bOPV |
| Seroprotection rates after the booster vaccination | 28-60 days after the booster dose (4 years old) of polio vaccine | The percentage of participants with positive antibody(titre ≥ 8) against all three serotypes of poliovirus |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Safety of the booster dose of polio vaccine immunization | 30 days after the booster vaccination | the occurrence of adverse events for the booster dose of Polio vaccine administered at age 4 using Sabin IPV or bOPV |
| Antibody titers pesistence against poliovirus | 3 years after the primary three doses of polio immunization(before the booster vaccination ) | Geometric Mean Titres (GMTs) or Median antibody titers for three poliovirus types |
| Antibody titers against poliovirus after the booster immunization | 28-60 days after the booster dose of polio vaccine given | Geometric Mean Titres (GMTs) or Median antibody titers for three poliovirus types after the booster dose of Polio vaccine administered at age 4 using Sabin IPV or bOPV |
Countries
China
Outcome results
None listed