Examining Factors That May Influence Resistance to HIV-1 Infection

Official Title: “Prospective Study of the Determinants of Host Resistance to HIV-1 Infection”

Some people who are exposed to the HIV-1 virus are capable of either controlling or completely preventing viral infection. Multiple genetic factors may contribute to preventing or controlling HIV-1 infection. The purpose of this study is to analyze the immune system responses of individuals who are exposed to HIV-1 but remain uninfected.

Even with repeated exposure to HIV-1, some individuals appear to be resistant to infection.

The exact mechanism of this resistance, however, remains unknown. The relative risk of HIV-1 infection appears to depend on various factors: route of transmission, viral load of the infected donor, nature and extent of exposure, presence of sexually transmitted infections (STIs), and genetic and immunological status of the exposed individual. This last factor may explain the inherent ability of some people to remain uninfected despite repeated exposure to HIV-1.

Immune response in HIV-1 exposed uninfected individuals is sometimes characterized by specific cytotoxic CD8 T cell response without antibody response, suggesting that resistance may, in part, be mediated by HIV-1 specific T cells. Exposed uninfected individuals may also be genetically protected, in which case key genes—possibly linked to immune responses—may lead to resistance to HIV-1. A clearer understanding of the role of an individual's genetic and immune-mediated resistance to HIV-1 infection is needed and will provide important information for advancing preventive HIV vaccine design. The purpose of this study is to examine the immune responses of individuals who have been exposed to HIV-1, but who remain uninfected. Through the use of highly sensitive technology, low level immune responses and viral levels will be evaluated. The study will also compare genetic profiles, exposure characteristics, donor viral load, STIs, and sexual behaviors among all participants. In the infected member of a serodiscordant couple, the HIV-1 virus will be examined and sequenced.

This observational study will last approximately 24 months. Screening will involve at least one visit and will occur at least 8 weeks prior to study entry. Eligible participants will fall into one of three groups: - Group 1 will include individuals who have been exposed to HIV-1 but who remain uninfected. - Group 2 will include HIV infected regular sexual partners of Group 1 members. - Group 3 will include HIV uninfected individuals or couples who have not been exposed to HIV-1.

Study visits will occur every 3 months for a total of 8 visits. At all visits, participants will verify address location, complete standardized questionnaires about sexual behaviors, and receive HIV safe sex counseling and free condoms. Blood and urine will be collected to test for HIV, STIs, and pregnancy. All participants will undergo a review of their medical history and a physical examination, including a genital exam for both males and females and a pelvic exam for females. At selected visits, participants may opt to provide additional samples of urine, saliva, genital secretions, breastmilk, and feces for research purposes.

Groups 1 and 3 will have HIV testing at all but the first study visit; Group 2 will have no HIV testing, but will be assessed for CD4 cell count at all study visits. Participants requiring clinical care for the management of HIV or STIs will be either treated at the study site or referred for appropriate care.

Arms, Groups and Cohorts in this Clinical Trial

• : 1
  • Inidividuals who have been exposed to HIV but remain uninfected.
• : 2
  • HIV infected regular sexual partners of Group 1 participants.
• : 3
  • HIV uninfected individuals or couples who have not been exposed to HIV.

Inclusion Criteria for Groups 1, 2, and 3:

• Willing to provide adequate location information
• Planning to remain in the area for the duration of the study

Inclusion Criteria for Group 1:

• HIV-1 antibody positive AND nucleic acid test (NAT) or p24 antigen negative
• Report unprotected receptive or insertive vaginal, oral, or anal intercourse with Group 2 partner on at least 12 occasions (St. Mary's cohort) or 25 occasions (MRC/UVRI Uganda cohort) during the 12 months prior to screening; the first sexual exposure with Group 2 partner must have occurred at least 10 months prior to screening

Inclusion Criteria for Group 2 (St. Mary's cohort):

• HIV-1 infected at screening, as determined by enzyme immunoassay and western blot
• Documentation of HIV-1 infection for at least 12 months prior to screening, as determined by enzyme immunoassay and western blot
• Willing to provide clinical information about HIV-1 RNA and CD4 cell count
• Report unprotected receptive or insertive vaginal, oral, or anal intercourse with Group 1 partner on at least 12 occasions during the 12 months prior to screening; the first sexual exposure with Group 1 partner must have occurred at least 10 months prior to screening

Inclusion Criteria for Group 2 (MRC/UVRI Uganda cohort):

• HIV-1 infected, as determined by enzyme immunoassay and western blot
• Report unprotected receptive or insertive vaginal, oral, or anal intercourse with Group 1 partner on at least 25 occasions during the 12 months prior to screening; the first sexual exposure with Group 1 partner must have occurred at least 10 months prior to screening
• HIV-1 infected for at least 12 months prior to screening, as determined by one of the following criteria:
• 1. Report a past medical history indicating Herpes zoster infection within the prior 5 years or report a medical history indicating WHO Clinical Staging
• Criteria for HIV/AIDS of III or IV within the prior 5 years, OR
• 2. CD4 cell count no greater than 450/mm3 for females or no greater than 400/mm3 for males
• Report no prior HIV testing, test HIV-1 seropositive at screening, and meet one of the following criteria:
• 1. Report a past medical history indicating Herpes zoster infection within the prior 5 years or report a past medical history indicating WHO Clinical Staging
• Criteria for HIV/AIDS of III or IV in the prior 5 years, OR
• 2. CD4 cell count no greater than 450/mm3 for females or no greater than 400/mm3 for males

Inclusion Criteria for Group 3:

• HIV-1 antibody negative AND nucleic acid test (NAT) or p24 antigen negative
• Test negative for Neisseria gonorrhoeae, syphilis, Chlamydia trachomatis, and trichomoniasis (MRC/UVRI Uganda cohort only)
• Report a monogamous relationship of at least 12 months duration prior to screening

Exclusion Criteria for Groups 1, 2, and 3:

• Injection drug use in the 5 years prior to screening
• Any condition that, in the opinion of the investigator, would be unsafe or interfere with the study
• Any obligations that may require long absences from the area

Gender Eligibility for this Clinical Trial: Both

Minimum Age for this Clinical Trial: 18 Years

Maximum Age for this Clinical Trial: N/A

Are Healthy Volunteers Accepted for this Clinical Trial?: Accepts Healthy Volunteers

Lead Investigator: National Institute of Allergy and Infectious Diseases (NIAID) NIH

Overall Clinical Trial Officials and Contacts

Andrew J. McMichael, MD, PhD Study Chair University of Oxford, Weatherall Institute of Molecular Medicine  

Information obtained from ClinicalTrials.gov on February 12, 2012

Link to the current ClinicalTrials.gov record. http://clinicaltrials.gov/show/NCT00351442

Study ID Number: CHAVI 002

ClinicalTrials.gov Identifier: NCT00351442

Health Authority: United States: Federal Government

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