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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
University of Cape Town
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional basic science trial for HIV Exposure focused on measuring Vaccine immunogenicity, Immune activation

Eligibility Criteria

undefined - 24 Hours (Child)All SexesAccepts Healthy Volunteers

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

    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
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    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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