Analysis of Immune Responses to HIV Vaccines
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This study will evaluate a test designed to measure immune system responses to HIV and HIV vaccines.
Condition |
---|
Acquired Immunodeficiency Syndrome HIV Infections |
Study Type: | Observational |
Study Design: | Observational Model: Defined Population Observational Model: Natural History Time Perspective: Cross-Sectional Time Perspective: Retrospective/Prospective |
Official Title: | Flow Cytometry Study of T Cell Responses to HIV Vaccines |
Estimated Enrollment: | 200 |
Study Start Date: | April 2003 |
Assays for HIV-specific human CD4 and CD8 T cell immunity are needed in order to evaluate the immune response to HIV vaccines. Such assays should be robust, reproducible, and amenable to high throughput analysis of clinical specimens. Cytokine flow cytometry (CFC) assays can reliably and specifically detect human CD4 and CD8 T cell responses to AIDS-related opportunistic infections, including those caused by cytomegalovirus, Mycobacterium tuberculosis, the Mycobacterium avium complex, cryptococcus, and human papillomavirus. The purpose of this study is to devise and evaluate a similar CFC assay for the detection and quantitation of CD4 and CD8 T cell responses against HIV.
This study will evaluate a "Gag-IFNg CFC" assay by comparing the results of this assay with results from other assays of immune phenotype and function in long-term nonprogressors, untreated patients with progressive HIV disease, and recipients of candidate HIV vaccines. The study will also examine HIV-specific immune responses in HIV infected individuals who appear to exhibit significant immune protection from HIV disease.
Participants in this study will be drawn from other studies currently underway. As a part of those studies, participants will have regular blood tests. Blood samples from those studies will be used in this study. No participants will be directly enrolled in this study.
![](https://webarchive.library.unt.edu/web/20130315211838im_/http://clinicaltrials.gov/ct2/html/images/frame/triangle.gif)
Genders Eligible for Study: | Both |
Accepts Healthy Volunteers: | Yes |
Blood samples from 5 cohorts of HIV infected individuals and 2 cohorts of HIV uninfected individuals will be evaluated.
Varying stages of HIV disease are represented in these cohorts, including:
- Individuals who have been exposed but who have not seroconverted
- Individuals who have recently seroconverted
- HAART-treated patients who receive immune modulators such as IL-2 and therapeutic immunization
- HAART-treated patients who undergo structured treatment interruptions
- HAART-treated patients who have durable suppression of viremia
- HAART-treated patients who experience incomplete suppression of viremia
- HAART-treated patients followed with careful drug adherence monitoring
- Long-term nonprogressors
- Untreated progressors
![](https://webarchive.library.unt.edu/web/20130315211838im_/http://clinicaltrials.gov/ct2/html/images/frame/triangle.gif)
United States, California | |
Core Immunology Laboratory | |
San Francisco, California, United States, 94103 |
Principal Investigator: | Joseph M. McCune, MD, PhD | University of California at San Francisco |
![](https://webarchive.library.unt.edu/web/20130315211838im_/http://clinicaltrials.gov/ct2/html/images/frame/triangle.gif)
Additional Information:
Publications:
ClinicalTrials.gov Identifier: | NCT00068978 History of Changes |
Other Study ID Numbers: | 5R01AI47062-03, 5 R01 AI47062-03 |
Study First Received: | September 12, 2003 |
Last Updated: | September 17, 2007 |
Health Authority: | United States: Federal Government |
Keywords provided by National Institute of Allergy and Infectious Diseases (NIAID):
HIV Seronegativity HIV Preventive Vaccine HIV Therapeutic Vaccine |
Additional relevant MeSH terms:
Acquired Immunodeficiency Syndrome HIV Infections Immunologic Deficiency Syndromes Lentivirus Infections Retroviridae Infections RNA Virus Infections |
Virus Diseases Sexually Transmitted Diseases, Viral Sexually Transmitted Diseases Slow Virus Diseases Immune System Diseases |
ClinicalTrials.gov processed this record on March 14, 2013