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Clinical Trials/NCT03519373
NCT03519373
Completed
Not Applicable

Impact of HIV Infection and Pregnancy on Humoral Responses to Pertussis Immunization

Centre Hospitalier Universitaire Saint Pierre2 sites in 1 country135 target enrollmentMarch 1, 2017

Overview

Phase
Not Applicable
Intervention
TDaP
Conditions
Immunization; Infection
Sponsor
Centre Hospitalier Universitaire Saint Pierre
Enrollment
135
Locations
2
Primary Endpoint
Pertussis-specific antibodies GMC after immunization
Status
Completed
Last Updated
last year

Overview

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.

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: 1. 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. 2. 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.

Registry
clinicaltrials.gov
Start Date
March 1, 2017
End Date
June 1, 2019
Last Updated
last year
Study Type
Observational
Sex
Female

Investigators

Sponsor
Centre Hospitalier Universitaire Saint Pierre
Responsible Party
Principal Investigator
Principal Investigator

Nicolas Dauby

M.D. Ph.D.

Centre Hospitalier Universitaire Saint Pierre

Eligibility Criteria

Inclusion Criteria

  • Age over 18
  • HIV-infected or uninfected pregnant women in their second/third trimester with an indication of TDaP vaccination
  • 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

  • Grade III/IV anemia
  • Active bacterial infection
  • Opportunistic infection (Tuberculosis, CMV, toxoplasmosis, etc)
  • Inability to understand the nature and extent of the study and the procedures required
  • Current or recent use of immunosuppressive drugs (corticosteroids, anti-TNF, methotrexate, etc)
  • Active neoplasia

Arms & Interventions

PER001

HIV 1-infected pregnant women

Intervention: TDaP

PER002

HIV 1-uninfected pregnant women

Intervention: TDaP

PER003

HIV 1-uninfected non-pregnant women

Intervention: TDaP

Outcomes

Primary Outcomes

Pertussis-specific antibodies GMC after immunization

Time Frame: 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

Time Frame: Birth

Anti-PT, FHA and PRN specific antibodies levels transfer ratio

Secondary Outcomes

  • Pertussis-specific memory B cells quantification & phenotype(7-10 days, 30 days and at delivery for pregnant women)
  • Pertussis-specific antibodies glycosylation profiles(7-10 days, 30 days and at delivery for pregnant women)

Study Sites (2)

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