ISST-002 EF-UP: Observational Study for the Extended Follow-up of the Patients Enrolled in the Therapeutic Clinical Trial ISS T-002

Sponsor
Barbara Ensoli, MD, PhD (Other)
Overall Status
Completed
CT.gov ID
NCT02118168
Collaborator
(none)
93
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39
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Study Details

Study Description

Brief Summary

An observational study to prospectively follow-up the patients enrolled in the ISS T-002 clinical trial up to 132 weeks. The primary endpoint of this study is to evaluate the persistence, in term of frequency, magnitude and quality, of the anti-Tat humoral and cellular immune response in the HIV-1 infected individuals who participated to the ISS T-002 and who have received at least 3 immunizations. The secondary endpoint is to define and validate novel laboratory tests for future efficacy clinical trials.

Condition or Disease Intervention/Treatment Phase
  • Other: No intervention

Study Design

Study Type:
Observational
Actual Enrollment :
93 participants
Observational Model:
Other
Time Perspective:
Prospective
Official Title:
OBSERVATIONAL STUDY FOR THE EXTENDED FOLLOW-UP OF THE PATIENTS ENROLLED IN THE PHASE II THERAPEUTIC CLINICAL TRIAL ISS T-002
Study Start Date :
Sep 1, 2013
Actual Primary Completion Date :
Jul 1, 2016
Actual Study Completion Date :
Dec 1, 2016

Arms and Interventions

Arm Intervention/Treatment
No treatment

All patients that participated to the therapeutic phase II trial of the Tat vaccine "ISS T-002" and that received at least 3 immunizations and reached 48-weeks of follow-up.

Other: No intervention
No intervention is foreseen in this Observational Study

Outcome Measures

Primary Outcome Measures

  1. anti-Tat humoral immune response [Every 3 months, up to 2.5 years]

    The primary endpoint of the study is to evaluate the persistence, in term of frequency, magnitude, and quality of the anti-Tat humoral immune response in HAART-treated patients previously immunize with Tat in the ISS T-002 phase II clinical trial.

Secondary Outcome Measures

  1. Testing of the additional Immunological parameters detailed below as a second line testing [Every 3 months, up to 2.5 years]

    The secondary endpoint of the study is to identify and validate immunological testing for future efficacy vaccine clinical trials, as follows: Lymphoproliferative response to Tat, anti-Tat γIFN, IL4 and IL2 production; In vitro neutralization of Tat activity (Tat/Env uptake); Lymphocyte subsets; Anti-Tat IgG subclasses; Epitope mapping of anti-Tat IgM and IgG; Anti-HIV regulatory and structural proteins antibodies; ADCC; Neutralization of Tat activity by rescue assay; Neutralization of primary HIV isolates; Anti-CCR5 and Anti-CD4 antibodies; Lymphoproliferative response to Env, mitogens and recall antigens In vitro γIFN, IL4 and IL2 production in response to Tat (ICS) and to Env (ICS/Elispot); B cells phenotype; Characterization of Treg cells; PBMC ICS for granzyme, perforin, cytokines and chemokines; Th1 and Th2 cytokines and chemokines; Lymphocytes spontaneous cell death; B cell cloning; Characterization of clono-specific antibodies; Serum/plasma determination of sCD4.

  2. Testing of virological parameters detailed below, as a second line testing [Every 3 months, up to 2.5 years]

    The secondary endpoint of the study is to identify and validate virological testing for future efficacy vaccine clinical trials, as follows: HIV-1 plasma viremia (viral RNA copies), HIV-1 sequencing and virus phylogenetic analysis, Genotypic resistance, Viral tropism, Anti-HBV antibodies, HBV antigens (HbsAg, HbeAg), Anti-HCV antibodies and plasma viremia, HHV-8 antibodies and plasma viremia, HIV-1 Proviral DNA copies.

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • Previous participation in the ISS T-002 trial, having received at least 3 immunizations;

  • A follow-up of at least 48 weeks during the ISS T-002 study;

  • Availability to participate in the extended follow-up study;

  • Signed informed consent.

Exclusion Criteria:
  • The absence of any of the above criteria will exclude the subjects from the study.

Contacts and Locations

Locations

Site City State Country Postal Code
1 Divisione di Malattie Infettive Azienda Ospedaliera S. Gerardo Monza MB Italy 20052
2 Divisione Malattie Infettive - AO Ospedale Policlinico Consorziale Bari Italy 70124
3 Ambulatorio Malattie Infettive - AO Universitaria Ferrara Italy 44124
4 Unità Operativa di Malattie Infettive - Ospedale S.M. Annunziata Firenze Italy 50012
5 U. O. di Malattie Infettive Centro di Ricerca e Cura Patologie HIV correlate - Ospedale San Raffaele Milano Italy 20124
6 Istituto di Malattie Infettive e Tropicali - AO Luigi Sacco Milano Italy 20152
7 Divisione di Malattie Infettive - AO Universitaria Policlinico Modena Italy 41100
8 U.O.C. Dermatologia Infettiva ed Allergologica - IFO San Gallicano Roma Italy 00144

Sponsors and Collaborators

  • Barbara Ensoli, MD, PhD

Investigators

  • Study Director: Barbara Ensoli, MD, PHD, Istituto Superiore di Sanità

Study Documents (Full-Text)

None provided.

More Information

Publications

Responsible Party:
Barbara Ensoli, MD, PhD, PhD, Istituto Superiore di Sanità
ClinicalTrials.gov Identifier:
NCT02118168
Other Study ID Numbers:
  • ISS T-002 EF-UP
First Posted:
Apr 21, 2014
Last Update Posted:
Aug 22, 2017
Last Verified:
Aug 1, 2017
Keywords provided by Barbara Ensoli, MD, PhD, PhD, Istituto Superiore di Sanità
Additional relevant MeSH terms:

Study Results

No Results Posted as of Aug 22, 2017