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The Effect of Bacille Calmette Guerin (BCG) Vaccination on Immune Responses in HIV-Exposed and Unexposed Infants

The Effect of BCG Vaccination on Immune Responses in HIV-Exposed and Unexposed Infants

Status
UNKNOWN
Phases
Phase 1Phase 2
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00331474
Enrollment
180
Registered
2006-05-31
Start date
2006-05-31
Completion date
2009-08-31
Last updated
2009-02-16

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

HIV Infections

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

BIOLOGICALBCG delayed

early (birth) and delayed (14 weeks) intradermal BCG vaccination

Sponsors

Thrasher Research Fund
CollaboratorOTHER
University of Stellenbosch
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
No minimum to 48 Hours
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

Design outcomes

Primary

MeasureTime frame
BCG-induced cellular immune responses1 year

Secondary

MeasureTime frame
BCG scarring18 months
Serum antibody responses52 weeks
Tuberculosis incidence1 year

Countries

South Africa

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026