Antibody Responses to Pneumococcal Vaccines Among HIV-Infected Adults.
Primary Purpose
HIV Infections
Status
Completed
Phase
Phase 2
Locations
Study Type
Interventional
Intervention
7-valent pneumococcal conjugate vaccine (vaccine)
23-valent pneumococcal conjugate vaccine (vaccine)
Sponsored by

About this trial
This is an interventional prevention trial for HIV Infections focused on measuring HIV infections, Pneumococcal vaccines, Treatment Experienced, Treatment Naive
Eligibility Criteria
Inclusion Criteria: Adult patients with proven HIV-1 infection Naïve or antiretroviral experienced CD4 cell count between 200 and 500/mm3 Plasma HIV RNA load lower than 4 log10 copies/mL Signed written informed consent Exclusion Criteria: Immunotherapy Immunization with the PPV within the past 5 years Splenectomy Use of intravenous immunoglobulin within the past 2 months Chemotherapy or radiation Any other vaccination within the past 2 months Severe renal failure End-stage liver disease Pregnancy
Sites / Locations
Outcomes
Primary Outcome Measures
Proportion of patients responders to 7 pneumococcal polysaccharides at W8
Secondary Outcome Measures
Persistence of antibody responses at W24 and W96
Clinical tolerance of pneumococcal vaccines at W8
Evolution of the CD4 count and plasma HIV RNA load
Immunological substudy (predictive factors of the antibody responses) at W24
Full Information
NCT ID
NCT00148824
First Posted
September 7, 2005
Last Updated
March 20, 2008
Sponsor
French National Agency for Research on AIDS and Viral Hepatitis
Collaborators
Wyeth is now a wholly owned subsidiary of Pfizer
1. Study Identification
Unique Protocol Identification Number
NCT00148824
Brief Title
Antibody Responses to Pneumococcal Vaccines Among HIV-Infected Adults.
Official Title
Immunological Efficacy of a Prime-Boost Strategy Combining a 7-Valent Pneumococcal Conjugate Vaccine (PCV) Followed by a 23-Valent Pneumococcal Polysaccharide Vaccine (PPV) Versus PPV Alone in HIV-Infected Adults. ANRS 114 PNEUMOVAC.
Study Type
Interventional
2. Study Status
Record Verification Date
March 2008
Overall Recruitment Status
Completed
Study Start Date
February 2003 (undefined)
Primary Completion Date
undefined (undefined)
Study Completion Date
January 2006 (Actual)
3. Sponsor/Collaborators
Name of the Sponsor
French National Agency for Research on AIDS and Viral Hepatitis
Collaborators
Wyeth is now a wholly owned subsidiary of Pfizer
4. Oversight
5. Study Description
Brief Summary
Streptococcus pneumoniae is the major cause of bacterial infection in HIV-infected patients. The current pneumococcal vaccine is poorly efficacious in patients with a CD4 cell count lower than 500/mm3. This study will test the efficacy and safety of a new pneumococcal vaccine strategy in patients with a CD4 cell count between 200 and 500/mm3.
Detailed Description
Streptococcus pneumoniae (SP) is the major cause of bacterial infection in HIV-infected patients. The 23-valent pneumococcal polysaccharide (PPV) is poorly immunogenic in patients with CD4 below 500 cells/mm3. The purpose of this multicentric national study is to evaluate whether a prime with a 7-valent pneumococcal conjugate vaccine (PCV), able to induce immunological memory, would improve immunogenicity against SP polysaccharides. 212 HIV-1 infected patients, with a CD4 count between 200 and 500/mm3, will be randomly assigned to one of two vaccine groups: PCV at Week 0 followed by PPV at Week 4 or PPV alone at Week 4. Evaluation will be done at week 8. The primary endpoint is the proportion of patients who had antibody responses against 7 pneumococcal polysaccharides at Week 8. Secondary endpoints include the persistence of antibody responses at Weeks 24 and 96, vaccines safety and occurrence of pneumococcal disease over time.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
HIV Infections
Keywords
HIV infections, Pneumococcal vaccines, Treatment Experienced, Treatment Naive
7. Study Design
Primary Purpose
Prevention
Study Phase
Phase 2
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
212 (false)
8. Arms, Groups, and Interventions
Intervention Type
Biological
Intervention Name(s)
7-valent pneumococcal conjugate vaccine (vaccine)
Intervention Type
Biological
Intervention Name(s)
23-valent pneumococcal conjugate vaccine (vaccine)
Primary Outcome Measure Information:
Title
Proportion of patients responders to 7 pneumococcal polysaccharides at W8
Secondary Outcome Measure Information:
Title
Persistence of antibody responses at W24 and W96
Title
Clinical tolerance of pneumococcal vaccines at W8
Title
Evolution of the CD4 count and plasma HIV RNA load
Title
Immunological substudy (predictive factors of the antibody responses) at W24
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Adult patients with proven HIV-1 infection
Naïve or antiretroviral experienced
CD4 cell count between 200 and 500/mm3
Plasma HIV RNA load lower than 4 log10 copies/mL
Signed written informed consent
Exclusion Criteria:
Immunotherapy
Immunization with the PPV within the past 5 years
Splenectomy
Use of intravenous immunoglobulin within the past 2 months
Chemotherapy or radiation
Any other vaccination within the past 2 months
Severe renal failure
End-stage liver disease
Pregnancy
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Philippe Lesprit, MD
Organizational Affiliation
Service d'Immunologie Clinique, Créteil, 94010, France
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Geneviève Chêne, MD, PhD
Organizational Affiliation
INSERM unité 593
Official's Role
Study Director
12. IPD Sharing Statement
Citations:
PubMed Identifier
20210645
Citation
Rabian C, Tschope I, Lesprit P, Katlama C, Molina JM, Meynard JL, Delfraissy JF, Chene G, Levy Y; ANRS 114 Pneumovac Study Group. Cellular CD4 T cell responses to the diphtheria-derived carrier protein of conjugated pneumococcal vaccine and antibody response to pneumococcal vaccination in HIV-infected adults. Clin Infect Dis. 2010 Apr 15;50(8):1174-83. doi: 10.1086/651418.
Results Reference
derived
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Antibody Responses to Pneumococcal Vaccines Among HIV-Infected Adults.
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