The Effect of Bacille Calmette Guerin (BCG) Vaccination on Immune Responses in HIV-Exposed and Unexposed Infants
Recruitment status was Active, not recruiting
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Purpose
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.
| Condition | Intervention | Phase |
|---|---|---|
|
HIV Infections |
Biological: BCG delayed |
Phase 1 Phase 2 |
| Study Type: | Interventional |
| Study Design: | Allocation: Randomized Endpoint Classification: Safety/Efficacy Study Intervention Model: Parallel Assignment Masking: Open Label Primary Purpose: Prevention |
| Official Title: | The Effect of BCG Vaccination on Immune Responses in HIV-Exposed and Unexposed Infants |
- BCG-induced cellular immune responses [ Time Frame: 1 year ] [ Designated as safety issue: No ]
- BCG scarring [ Time Frame: 18 months ] [ Designated as safety issue: No ]
- Serum antibody responses [ Time Frame: 52 weeks ] [ Designated as safety issue: No ]
- Tuberculosis incidence [ Time Frame: 1 year ] [ Designated as safety issue: No ]
| Estimated Enrollment: | 180 |
| Study Start Date: | May 2006 |
| Estimated Study Completion Date: | August 2009 |
| Primary Completion Date: | December 2008 (Final data collection date for primary outcome measure) |
-
Biological: BCG delayed
Eligibility| Ages Eligible for Study: | up to 48 Hours |
| Genders Eligible for Study: | Both |
| 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
Contacts and Locations| South Africa | |
| Desmond Tutu TB Centre | |
| Cape Town, Western Cape Province, South Africa, 7505 | |
| Principal Investigator: | Anneke C Hesseling, MD | Desmond Tutu TB Centre, Dept. Pediatrics and Child Health, Stellenbosch University |
More Information
No publications provided
| Responsible Party: | Esther Steyn or Liesel Strauss, Stellenbosch University |
| ClinicalTrials.gov Identifier: | NCT00331474 History of Changes |
| Other Study ID Numbers: | N06/04/071 |
| Study First Received: | May 30, 2006 |
| Last Updated: | February 13, 2009 |
| Health Authority: | South Africa: Human Research Ethics Committee |
Keywords provided by University of Stellenbosch:
|
BCG HIV Immune responses Delayed vaccination |
Infant morbidity Nutritional status Morbidity Mortality |
Additional relevant MeSH terms:
|
HIV Infections Acquired Immunodeficiency Syndrome Lentivirus Infections Retroviridae Infections RNA Virus Infections Virus Diseases |
Sexually Transmitted Diseases, Viral Sexually Transmitted Diseases Immunologic Deficiency Syndromes Immune System Diseases Slow Virus Diseases |
ClinicalTrials.gov processed this record on June 18, 2013