HIV Infections
Conditions
Keywords
BCG, HIV, Immune responses, Delayed vaccination, Infant morbidity, Nutritional status, Morbidity, Mortality
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.
Interventions
early (birth) and delayed (14 weeks) intradermal BCG vaccination
Sponsors
Study design
Eligibility
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
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| BCG-induced cellular immune responses | 1 year |
Secondary
| Measure | Time frame |
|---|---|
| BCG scarring | 18 months |
| Serum antibody responses | 52 weeks |
| Tuberculosis incidence | 1 year |
Countries
South Africa