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Clinical Trials/NCT00331474
NCT00331474UnknownPhase 1

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

University of Stellenbosch2 sites in 1 country180 target enrollmentStarted: May 1, 2006Last updated:
Conditions

Trial Snapshot

Phase
Phase 1
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)

Investigators

Sponsor Class
Other

Study Sites (2)

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