Observational Study on Anti-Tat Immune Response in HIV-1-infected Asymptomatic Adult Subjects (ISS OBS T-003)
This study has been completed.
Sponsor:
Barbara Ensoli, MD
Information provided by (Responsible Party):
Barbara Ensoli, MD, Istituto Superiore di Sanità
ClinicalTrials.gov Identifier:
NCT01029548
First received: December 9, 2009
Last updated: March 3, 2016
Last verified: March 2016
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Purpose
The present study is designed as a prospective observational study directed at evaluating the frequency, magnitude, quality and persistence (primary endpoint) of the anti-Tat immune response in HIV-1 infected asymptomatic individuals, and to prospectively evaluate the immunological, virological and clinical outcome of anti-Tat positive versus anti-Tat negative drug naїve subjects (secondary endpoint) in order to determine the impact of anti-Tat immunity on HIV disease progression as well as the potential use of anti-Tat immune response assessment for the clinical and therapeutic management of infected patients. This survey provided important information for the design, planning and conduction of future therapeutic vaccine trials based on the HIV-1 Tat protein in asymptomatic subjects.
| Condition |
|---|
| HIV Infections |
| Study Type: | Observational |
| Study Design: | Observational Model: Cohort Time Perspective: Prospective |
| Official Title: | Observational Study With Additional Diagnostic Procedures on Anti-Tat Immune Response in HIV-1-infected Asymptomatic Adult Subjects |
Resource links provided by NLM:
Further study details as provided by Barbara Ensoli, MD, Istituto Superiore di Sanità:
Primary Outcome Measures:
- Specific humoral and cellular immune responses to Tat will be monitored by assessing anti-Tat specific antibodies in sera, proliferative response (CFSE) and production of γIFN, IL-4 and IL-2 (Elispot) by peripheral blood mononuclear cells.
Secondary Outcome Measures:
- The decline of CD4+ T cells count, the increase of the HIV plasma viral load or the occurrence of AIDS-defining events will be assessed to determine the progression to disease
Biospecimen Retention: Samples With DNA
Whole Blood, serum, PBMCs
| Enrollment: | 73 |
| Study Start Date: | April 2008 |
| Study Completion Date: | May 2012 |
Eligibility| Ages Eligible for Study: | 18 Years and older (Adult, Senior) |
| Sexes Eligible for Study: | All |
| Accepts Healthy Volunteers: | No |
| Sampling Method: | Non-Probability Sample |
Study Population
Asymptomatic HIV infected individuals
Criteria
Inclusion Criteria:
- To be clinically asymptomatic HIV-1 infected individuals with CD4+ T cell counts ≥400/μL
- To be naïve for antiretroviral therapy
- Levels of plasma viremia ≤100,000 copies/ml at baseline
- Age ≥ 18 years
- Signed informed consent
Exclusion Criteria:
- Current therapy with immunomodulators or immunosuppressive drugs or chemotherapy for neoplastic disorders
- Concomitant treatment for HBV or HCV infection
Contacts and Locations
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Please refer to this study by its ClinicalTrials.gov identifier: NCT01029548
Please refer to this study by its ClinicalTrials.gov identifier: NCT01029548
Locations
| Italy | |
| S.M. Goretti Hospital | |
| Latina, Rome, Italy | |
| General Hospital of Bari | |
| Bari, Italy | |
| Spedali Civili di Brescia | |
| Brescia, Italy | |
| General Hospital-University of Ferrara | |
| Ferrara, Italy | |
| A.M. Annunziata Hospital | |
| Florence, Italy | |
| L. Sacco Hospital | |
| Milan, Italy | |
| San Raffaele Hospital | |
| Milan, Italy | |
| General Hospital-University of Modena | |
| Modena, Italy, 41100 | |
| San Gallicano Hospital | |
| Rome, Italy | |
| Giovanni Di Perri | |
| Turin, Italy, 10149 | |
Sponsors and Collaborators
Barbara Ensoli, MD
Investigators
| Principal Investigator: | Francesco Mazzotta, MD | A.M. Annunziata Hospital Florence, Italy |
| Principal Investigator: | Giuseppe Pastore, MD | General Hospital of Bari |
| Principal Investigator: | Florio Ghinelli, MD | General Hospital-University of Ferrara |
| Principal Investigator: | Roberto Esposito, MD | General Hospital-University of Modena |
| Principal Investigator: | Massimo Galli, MD | L.Sacco Hospital - MI |
| Principal Investigator: | Fabrizio Soscia, MD | S.M. Goretti Hospital Latina |
| Principal Investigator: | Guido Palamara, MD | San Gallicano Hospital - Rome |
| Principal Investigator: | Adriano Lazzarin, MD | San Raffaele Hospital - Milan |
| Principal Investigator: | Giampiero Carosi, MD | Spedali Civili - Brescia |
| Principal Investigator: | Giovanni Di Perri, MD | Amedeo di Savoia Hospital - Turin |
More Information
Additional Information:
Publications:
| Responsible Party: | Barbara Ensoli, MD, PhD, Istituto Superiore di Sanità |
| ClinicalTrials.gov Identifier: | NCT01029548 History of Changes |
| Other Study ID Numbers: |
ISS OBS T-003 |
| Study First Received: | December 9, 2009 |
| Last Updated: | March 3, 2016 |
Keywords provided by Barbara Ensoli, MD, Istituto Superiore di Sanità:
|
HIV Therapeutic Vaccine |
Additional relevant MeSH terms:
|
HIV Infections Lentivirus Infections Retroviridae Infections RNA Virus Infections Virus Diseases |
Sexually Transmitted Diseases, Viral Sexually Transmitted Diseases Immunologic Deficiency Syndromes Immune System Diseases |
ClinicalTrials.gov processed this record on July 17, 2017


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