Early Versus Delayed BCG Vaccination of HIV-exposed Infants
Primary Purpose
HIV Exposure, HIV Infection
Status
Completed
Phase
Phase 2
Locations
Study Type
Interventional
Intervention
BCG
Sponsored by

About this trial
This is an interventional basic science trial for HIV Exposure focused on measuring Vaccine immunogenicity, Immune activation
Eligibility Criteria
Inclusion Criteria:
- Healthy neonate
- Maternal HIV
- > 36 weeks gestation
- Birth weight > 2.4kg
- Remaining in area 4 months
Exclusion Criteria:
- Complications during pregnancy and delivery
- Household TB contacts
Sites / Locations
Arms of the Study
Arm 1
Arm 2
Arm Type
Active Comparator
Other
Arm Label
Delayed BCG
Early BCG
Arm Description
BCG delayed to 8 weeks of age
BCG at birth; standard of care
Outcomes
Primary Outcome Measures
T Cell Activation
Percentage of all CD4+ T cells expressing HLADR (NOT BCG-specific activation as in Tchakoute et al and as in secondary outcome). The n is smaller than the enrollment number as some participants were lost to follow-up, some were excluded due to HIV infection etc, and some samples did not have sufficient cells to analyse.
Secondary Outcome Measures
Vaccine Immunogenicity
Percent of CD4+ T cells expressing Ki67 after stimulation in vitro with BCG.
Full Information
NCT ID
NCT02062580
First Posted
February 12, 2014
Last Updated
January 25, 2017
Sponsor
University of Cape Town
Collaborators
Seattle Children's Research Institute (SCRI), University of Stellenbosch
1. Study Identification
Unique Protocol Identification Number
NCT02062580
Brief Title
Early Versus Delayed BCG Vaccination of HIV-exposed Infants
Official Title
Influence of BCG Immunization on Immune Responses and Disease Progression in South African HIV Exposed and Infected Infants
Study Type
Interventional
2. Study Status
Record Verification Date
January 2017
Overall Recruitment Status
Completed
Study Start Date
June 2010 (undefined)
Primary Completion Date
April 2012 (Actual)
Study Completion Date
undefined (undefined)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University of Cape Town
Collaborators
Seattle Children's Research Institute (SCRI), University of Stellenbosch
4. Oversight
Data Monitoring Committee
No
5. Study Description
Brief Summary
In sub-Saharan Africa (SSA), more than 300,000 babies with HIV die each year. HIV-infected children develop AIDS and die faster in SSA than those in developed countries. Bacille Calmette-Guerin (BCG) vaccine is given to infants at birth in SSA to protect them from severe forms of TB. BCG is known to cause immune cells to be active and replicate faster. The immune system of neonates also responds differently to BCG that to other vaccines and infections. We hypothesize that the routine immunization of neonates with BCG contributes to generalized immune activation in HIV-exposed infants resulting in skewed immune responses to vaccines and infections and increased rates of disease progression in those infants that become HIV-infected. However, delaying BCG until HIV testing is completed would result in operational difficulties, and may not induce the appropriate immune response. Delayed BCG would also render many HIV-exposed uninfected infants at high risk for disseminated TB. We plan to assess immune cells in infants to determine the impact of the timing of BCG vaccination on immune responses to tuberculosis (TB) and other vaccines. We will also compare the immune activation and disease progression of those infants that become HIV-infected in the BCG or control arms. Our results will provide key insights into the effect of BCG vaccination on immune responses to HIV as well as inform the optimal timing of BCG vaccination for HIV-exposed infants.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
HIV Exposure, HIV Infection
Keywords
Vaccine immunogenicity, Immune activation
7. Study Design
Primary Purpose
Basic Science
Study Phase
Phase 2
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
149 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Delayed BCG
Arm Type
Active Comparator
Arm Description
BCG delayed to 8 weeks of age
Arm Title
Early BCG
Arm Type
Other
Arm Description
BCG at birth; standard of care
Intervention Type
Biological
Intervention Name(s)
BCG
Primary Outcome Measure Information:
Title
T Cell Activation
Description
Percentage of all CD4+ T cells expressing HLADR (NOT BCG-specific activation as in Tchakoute et al and as in secondary outcome). The n is smaller than the enrollment number as some participants were lost to follow-up, some were excluded due to HIV infection etc, and some samples did not have sufficient cells to analyse.
Time Frame
at 6 weeks
Secondary Outcome Measure Information:
Title
Vaccine Immunogenicity
Description
Percent of CD4+ T cells expressing Ki67 after stimulation in vitro with BCG.
Time Frame
6 weeks after BCG vaccination
10. Eligibility
Sex
All
Maximum Age & Unit of Time
24 Hours
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria:
Healthy neonate
Maternal HIV
> 36 weeks gestation
Birth weight > 2.4kg
Remaining in area 4 months
Exclusion Criteria:
Complications during pregnancy and delivery
Household TB contacts
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Heather B Jaspan, MD, PHD
Organizational Affiliation
University of Cape Town
Official's Role
Principal Investigator
12. IPD Sharing Statement
Citations:
PubMed Identifier
28405623
Citation
Gasper MA, Hesseling AC, Mohar I, Myer L, Azenkot T, Passmore JS, Hanekom W, Cotton MF, Crispe IN, Sodora DL, Jaspan HB. BCG vaccination induces HIV target cell activation in HIV-exposed infants in a randomized trial. JCI Insight. 2017 Apr 6;2(7):e91963. doi: 10.1172/jci.insight.91963.
Results Reference
derived
PubMed Identifier
26259542
Citation
Blakney AK, Tchakoute CT, Hesseling AC, Kidzeru EB, Jones CE, Passmore JA, Sodora DL, Gray CM, Jaspan HB. Delayed BCG vaccination results in minimal alterations in T cell immunogenicity of acellular pertussis and tetanus immunizations in HIV-exposed infants. Vaccine. 2015 Sep 11;33(38):4782-9. doi: 10.1016/j.vaccine.2015.07.096. Epub 2015 Aug 7.
Results Reference
derived
PubMed Identifier
25108027
Citation
Tchakoute CT, Hesseling AC, Kidzeru EB, Gamieldien H, Passmore JA, Jones CE, Gray CM, Sodora DL, Jaspan HB. Delaying BCG vaccination until 8 weeks of age results in robust BCG-specific T-cell responses in HIV-exposed infants. J Infect Dis. 2015 Feb 1;211(3):338-46. doi: 10.1093/infdis/jiu434. Epub 2014 Aug 8.
Results Reference
derived
Learn more about this trial
Early Versus Delayed BCG Vaccination of HIV-exposed Infants
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