Safety of and Immune Response to a Combination HIV Vaccine Regimen in HIV Uninfected Adults
Study Details
Study Description
Brief Summary
To prevent HIV infection, a vaccine that produces strong HIV-specific humoral (B-cell) and cellular (T-cell) immune system responses is desirable. The purpose of this study is to test the safety of and immune response to a novel combination HIV vaccine in HIV uninfected adults. This study will also test the safety of and immune response to a protein vaccine given alone.
| Condition or Disease | Intervention/Treatment | Phase |
|---|---|---|
|
Phase 1 |
Detailed Description
The development of a vaccine eliciting HIV-specific humoral and cellular immune responses is desirable for the prevention of HIV infection. This study will investigate a combination vaccine regimen consisting of priming with DNA followed by boosting with a recombinant envelope glycoprotein adjuvanted in MF59.
All participants will be followed for 15 months. Participants enrolled in Groups 1, 2, 3, and 4 will receive either the vaccine or placebo. Study visits will be completed at initial entry; five visits every 14 days for the first 2.5 months; and visits at Months 4, 4.5, 6, 6.5, 9, 9.5, 12, and 15. All participants will undergo physical exams, urine collection, and blood tests to assess safety, HIV infection, and immune responses to injections. Risk reduction/pregnancy prevention counseling will be given at every study visit. Participants will also be asked to complete questionnaires about outside testing and beliefs at certain visits.
There are two parts to this study. In Part A, participants will be sequentially assigned to one of three groups. Each group will receive injections of different amounts of either DNA vaccine or placebo at entry, Month 1, and Month 2. This is followed by identical injections of glycoprotein/adjuvant or placebo at Months 6 and 9. Group 1 will receive 250 mcg each of the gag and env DNA plasmid with microparticle vaccine; Group 2 will receive 500 mcg of each vaccine; Group 3 will receive 1000 mcg of each vaccine. Participants will be enrolled sequentially from low to high dose beginning with Group 1.
In Part B, Group 4 will begin the second part of the study simultaneously after safety review of all participants in Part A. Group 4 participants will receive identical injections of either DNA vaccine or placebo at entry and at Months 1, 2, 6, and 9.
Group 5 will begin enrollment after enrollment is completed for Groups 1, 2, 3, and 4. Group 5 participants will receive identical injections of either glycoprotein/adjuvant or placebo at study entry and at Months 3 and 9. There will be 11 study visits for Group 5 participants; they will occur at screening, study entry, and Months 0.5, 2, 3, 3.5, 6, 9, 9.5, 12, and 15. A physical exam and risk reduction/pregnancy prevention counseling will occur at all visits; participants will be asked at every visit about any adverse events they may have experienced. Blood and urine collection will occur at selected visits. Participants will be also asked to complete questionnaires about outside testing and beliefs at certain visits.
Study Design
Outcome Measures
Primary Outcome Measures
- Safety (local and systemic reactogenicity signs and symptoms, laboratory measures, and adverse and serious experiences) []
- immunogenicity (presence of HIV-specific immune response as measured by the interferon-gamma ELISpot, FACS Intracellular Cytokine Staining [ICS], neutralizing antibody, or HIV antigen-binding ELISA assays) []
- social impacts (negative experiences or problems reported by the participants) []
Eligibility Criteria
Criteria
Note: As of 07/01/05, Group 5 will begin enrollment after enrollment into Groups 1, 2, 3, and 4 is completed.
Inclusion Criteria
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Understanding of vaccination procedure
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Willing to receive HIV test results and provide informed consent
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Good general health
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HIV negative
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Hepatitis B surface antigen negative
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Anti-hepatitis C virus (HCV) antibody negative, or negative for HCV PCR if the anti-HCV is positive
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Not pregnant and agrees to use acceptable forms of contraception
Exclusion Criteria
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Received HIV vaccines or placebo in a prior HIV vaccine trial
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Immunosuppressive medications within 168 days prior to study
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Blood products within 120 days prior to study
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Immunoglobulin within 60 days prior to study
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Live attenuated vaccines within 30 days prior to study
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Investigational research agents within 30 days prior to study
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Medically indicated subunit or killed vaccines within 14 days prior to study
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Current anti-tuberculosis prophylaxis or therapy
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Anaphylaxis or other serious adverse reactions to vaccines; a person who had an adverse reaction to pertussis vaccine as a child is not excluded
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Autoimmune disease or immunodeficiency
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Active syphilis infection
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Unstable asthma (e.g., use of oral, orally inhaled, or intravenous corticosteroids, emergent care, urgent care, hospitalization or intubation during the past 2 years)
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Diabetes mellitus; a participant with past gestational diabetes is not excluded
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Thyroid disease, including removal of thyroid and diagnoses requiring medication
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Serious angioedema
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Uncontrolled hypertension
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Diagnosis of bleeding disorder
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Malignancy, except those with a surgical excision and subsequent observation period that in the investigator's estimate has a reasonable assurance of sustained cure and/or is unlikely to recur during the period of the study
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Seizure disorder requiring medication within the last 3 years
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Absence of the spleen
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Mental illness that would interfere with compliance with the protocol
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Breastfeeding
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Unprotected rectal or vaginal sex with a partner known to be HIV infected within 6 months of enrollment
Contacts and Locations
Locations
| Site | City | State | Country | Postal Code | |
|---|---|---|---|---|---|
| 1 | Saint Louis Univ. School of Medicine, HVTU | Saint Louis | Missouri | United States | |
| 2 | Miriam Hospital's HVTU | Providence | Rhode Island | United States | 02906 |
| 3 | Vanderbilt Vaccine CRS | Nashville | Tennessee | United States | 37232 |
| 4 | FHCRC/UW Vaccine CRS | Seattle | Washington | United States | 98104 |
Sponsors and Collaborators
- National Institute of Allergy and Infectious Diseases (NIAID)
Investigators
- Study Chair: Paul Spearman, Vanderbilt University
- Study Chair: Michelle Lally, Brown University
Study Documents (Full-Text)
None provided.More Information
Publications
- Malkevitch NV, Robert-Guroff M. A call for replicating vector prime-protein boost strategies in HIV vaccine design. Expert Rev Vaccines. 2004 Aug;3(4 Suppl):S105-17. Review.
- O'Hagan D, Singh M, Ugozzoli M, Wild C, Barnett S, Chen M, Schaefer M, Doe B, Otten GR, Ulmer JB. Induction of potent immune responses by cationic microparticles with adsorbed human immunodeficiency virus DNA vaccines. J Virol. 2001 Oct;75(19):9037-43.
- O'Hagan DT, Ugozzoli M, Barackman J, Singh M, Kazzaz J, Higgins K, Vancott TC, Ott G. Microparticles in MF59, a potent adjuvant combination for a recombinant protein vaccine against HIV-1. Vaccine. 2000 Mar 6;18(17):1793-801.
- Slobod KS, Bonsignori M, Brown SA, Zhan X, Stambas J, Hurwitz JL. HIV vaccines: brief review and discussion of future directions. Expert Rev Vaccines. 2005 Jun;4(3):305-13. Review.
- Stratov I, DeRose R, Purcell DF, Kent SJ. Vaccines and vaccine strategies against HIV. Curr Drug Targets. 2004 Jan;5(1):71-88. Review.
- HVTN 049
- 10054