The Effect of BCG Vaccination on Immune Responses in HIV-Exposed and Unexposed Infants
Trial Snapshot
- Phase
- Phase 1
- Sponsor
- University of Stellenbosch
- Enrollment
- 180
- Locations
- 2
- Primary Endpoint
- BCG-induced cellular immune responses
Study Overview
Brief Summary
Background:
Each year, more than half a million babies are infected with HIV by mother-to child transmission in developing countries. Many of these babies get sick and develop HIV disease (AIDS) at a very young age. Exposure to other infectious diseases may influence this early progression to AIDS. BCG is a live tuberculosis vaccine made from cow tuberculosis. It is routinely given at birth to most babies, also to babies born to HIV-positive mothers. BCG can cause disease (BCGosis) in HIV-infected babies. More importantly, BCG may also trigger immune responses in the body that lead to the spread of the HIV virus and early progression to AIDS.
Objective(s) and Hypothesis:
The researchers will investigate whether BCG causes progression of HIV by doing a clinical trial: babies born to HIV-positive mothers will be randomly allocated to get the BCG vaccine at birth or at 14 weeks of age. In these 2 groups of babies, the researchers will compare:
- The percentage of babies who progress to HIV disease
- Blood markers of HIV disease (the amount of virus and protective white blood cells in the body)
- The body's immune response to BCG vaccine and other childhood vaccines
- The percentage of children who develop BCG scarring, BCG vaccine complications and tuberculosis.
Potential Impact:
BCG is the most widely given vaccine worldwide and is routinely given to babies born to HIV-positive mothers in developing countries. Any effect that BCG has on HIV progression in babies will have a significant public health impact in settings with a high burden of HIV disease.
Study Design
- Study Type
- Interventional
- Allocation
- Randomized
- Intervention Model
- Parallel
- Primary Purpose
- Prevention
- Masking
- None
Eligibility Criteria
- Ages
- — to 48 Hours (Child)
- Sex
- All
- Accepts Healthy Volunteers
- No
Inclusion Criteria
- •Maternal HIV status verified
- •Study consent
- •Uncomplicated singleton pregnancy with delivery planned at local health facility
- •Resident in study area
Exclusion Criteria
- •Active tuberculosis or tuberculosis contact in mother
- •No consent
- •Planning to move out of study area
- •Not planning on delivering at local maternal obstetric unit
- •Not planning on attending local baby clinic
Outcomes
Primary Outcomes
BCG-induced cellular immune responses
Time Frame: 1 year
Secondary Outcomes
- BCG scarring(18 months)
- Serum antibody responses(52 weeks)
- Tuberculosis incidence(1 year)
