Pertussis Immunization During Pregnancy & HIV Infection
Study Details
Study Description
Brief Summary
The impact of chronic HIV infection and pregnancy on different aspects of the humoral response to pertussis immunization with the TDaP vaccine will be studied. The parameters will be measured in 3 groups (HIV-infected pregnant, HIV-uninfected pregnant and HIV-uninfected non pregnant) at different time points before and after immunization (7-10 days, 30 days and at delivery). The transfer ratio and the quality of maternal antibodies will be studied in cord blood.
| Condition or Disease | Intervention/Treatment | Phase |
|---|---|---|
|
Detailed Description
Despite the growing importance of maternal immunization in the control of infectious pathogens in early life, the impact of pregnancy on vaccine immunogenicity remains poorly understood. Evidence suggests that pregnancy may influence the quality of the antibody response to vaccines. Pregnancy is associated with modifications in the glycosylation profile of immunoglobulins G (IgG). Different patterns of glycosylation are associated with differential regulation of the effector functions of IgG such as antibody-dependent cell cytotoxicity, complement activation or antibody dependent phagocytosis. Whether similar modifications affect vaccine-induced IgG in pregnant women is unknown.
HIV infection is associated with important alterations in B cells and antibodies. Although antiretroviral therapy partly corrects the proportions of memory B cells (MBC) subsets, it does not restore B cell responses to vaccines, measured as seroconversion rates and antibody persistence. Reduced IgG responses to vaccines have been observed in HIV-infected pregnant women but the impact of HIV on the quality of vaccine-induced IgG has not been reported. On the other hand, HIV infection in pregnancy has a strong impact on the transfer of maternal IgG to the newborn, possibly as a consequence of hypergammaglobulinemia and immune activation.
The investigators will:
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Assess the respective impact of pregnancy and HIV infection on the magnitude and quality of B cell and antibody responses to pertussis immunization with the TDaP vaccine.
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Assess the impact of HIV infection and of the timing of maternal immunization on the transplacental transfer and on the quality of pertussis-specific IgG in the newborn.
Study Design
Arms and Interventions
| Arm | Intervention/Treatment |
|---|---|
| PER001 HIV 1-infected pregnant women |
Biological: TDaP
Tetanus, Diphteria and Acellular Pertussis vaccine (Boostrix)
|
| PER002 HIV 1-uninfected pregnant women |
Biological: TDaP
Tetanus, Diphteria and Acellular Pertussis vaccine (Boostrix)
|
| PER003 HIV 1-uninfected non-pregnant women |
Biological: TDaP
Tetanus, Diphteria and Acellular Pertussis vaccine (Boostrix)
|
Outcome Measures
Primary Outcome Measures
- Pertussis-specific antibodies GMC after immunization [7-10 days, 30 days and at delivery for pregnant women]
Anti-Pertussis Toxin (PT), Filamentous Hemagglutinin (FHA) and pertactin (PRN) specific antibodies levels
- Transplacental transfer of pertussis-specific antibodies [Birth]
Anti-PT, FHA and PRN specific antibodies levels transfer ratio
Secondary Outcome Measures
- Pertussis-specific memory B cells quantification & phenotype [7-10 days, 30 days and at delivery for pregnant women]
PT, FHA and PRN-specific memory B cells numbers assessed by ELISPOT assay & Flow Cytometry
- Pertussis-specific antibodies glycosylation profiles [7-10 days, 30 days and at delivery for pregnant women]
Anti-PT, FHA and PRN specific antibodies profiles
Eligibility Criteria
Criteria
Inclusion Criteria:
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Age over 18
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HIV-infected or uninfected pregnant women in their second/third trimester with an indication of TDaP vaccination
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Non pregnant HIV negative women (having a negative HIV test in the last 6 months or at screening) with an indication of TDaP vaccination
Exclusion Criteria:
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Grade III/IV anemia
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Active bacterial infection
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Opportunistic infection (Tuberculosis, CMV, toxoplasmosis, etc)
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Inability to understand the nature and extent of the study and the procedures required
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Current or recent use of immunosuppressive drugs (corticosteroids, anti-TNF, methotrexate, etc)
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Active neoplasia
Contacts and Locations
Locations
| Site | City | State | Country | Postal Code | |
|---|---|---|---|---|---|
| 1 | CHU Saint-Pierre | Brussels | Belgium | 1000 | |
| 2 | HIS Etterbeek Ixelles | Ixelles | Belgium | 1050 |
Sponsors and Collaborators
- Centre Hospitalier Universitaire Saint Pierre
Investigators
- Principal Investigator: Nicolas Dauby, M.D. Ph.D., Centre Hospitalier Universitaire Saint Pierre
Study Documents (Full-Text)
None provided.More Information
Publications
None provided.- Pertussis