Actively Recruiting
Leukapheresis Procedures to Obtain Plasma and Lymphocytes for Research Studies on Antiretroviral Naive HIV-1 Research Participants
Led by National Institute of Allergy and Infectious Diseases (NIAID) · Updated on 2026-04-29
750
Participants Needed
1
Research Sites
N/A
Total Duration
On this page
AI-Summary
What this Trial Is About
There is evidence that early and aggressive treatment with antiretroviral drugs can prevent the loss of immune cell function that accompanies HIV infection. This study will use leukapheresis (drawing blood, separating out the white cells and returning the blood to the patient) to obtain blood cells from HIV-infected patients in either the acute or chronic stage of infection who are being treated with early highly active antiretroviral therapy (HAART). Leukapheresis is necessary to obtain enough cells to delineate the response of B cells to CD4+ T cell help, the CD8 factors associated with suppression of viral replication and normalization of immune function, and natural killer function relative to HIV disease. Study participants will be adult (older than 18 years) HIV primary or acutely affected patients (those with a history of exposure to HIV but not yet showing chronic symptoms of HIV disease) and HIV chronically infected patients (those infected with HIV for longer than 12 months or showing other symptoms of HIV disease) who are not receiving HAART at the beginning of the study. The study seeks to enroll 30 primary and 30 chronic patients. Pregnant women will not be enrolled in the study; women who become pregnant will be dropped from the study. Leukapheresis will be performed on each patient before HAART therapy begins and then three times a year. Each session will take between 1 and 3 hours. This longitudinal study will enable researchers to examine the function of certain B cells, natural killer cells, and CD8+ T cells in people who do not have chronic HIV disease and in those who do have the disease and are treated with HAART.
CONDITIONS
Official Title
Leukapheresis Procedures to Obtain Plasma and Lymphocytes for Research Studies on Antiretroviral Naive HIV-1 Research Participants
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Adult (18 years old or older) with HIV-1.
- Adequate venous access for research blood collection.
- Positive HIV antibody immunoassay and confirmatory HIV test or, for suspected early HIV-1, HIV-1 RNA >2,000 copies/ml with negative antibody test.
- Willingness to attend follow-up visits at least once in the next 4 months before starting antiretroviral therapy.
- Blood pressure less than 180/100 and pulse rate between 50-100 unless a lower pulse rate is normal for the participant.
- Adequate blood counts (hemoglobin ≥9.0 g/dL, hematocrit ≥28%, platelets ≥50,000).
- Willingness and ability to give informed consent including for blood sample storage and genetic testing.
- Antiretroviral naive, no antiretroviral use in the last six months, or previous enrollment with stored samples.
- Participants who acquired HIV-1 while on pre-exposure prophylaxis are eligible if meeting HIV positivity criteria.
- Participants enrolled under another LIR apheresis protocol within the past three months who completed apheresis within 4 weeks of starting ART are eligible.
- Participants with limited recent ART use (no more than 4 weeks before screening) may be eligible if it doesn't affect the study's scientific validity.
You will not qualify if you...
- Pregnant and/or breastfeeding.
- Currently abusing alcohol or drugs that could interfere with compliance or safety.
- Any condition that investigators believe makes the participant ineligible for the study.
AI-Screening
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Trial Site Locations
Total: 1 location
1
National Institutes of Health Clinical Center
Bethesda, Maryland, United States, 20892
Actively Recruiting
Research Team
K
Kathleen R Gittens
CONTACT
S
Susan L Moir, Ph.D.
CONTACT
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
2
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