Recruiting

Observational Study

Sponsor:

National Institute of Allergy and Infectious Diseases (NIAID)

Code:

NCT00001316

Conditions

HIV

Eligibility Criteria

Sex: All

Age: 18 - 70+

Healthy Volunteers: Accepted

Study Details

Brief summary:

This is a study to determine the effect of the human immunodeficiency virus (HIV) on lymphoid tissues (e.g., lymph nodes) as compared to peripheral white blood cells. We have shown in previous studies that the lymph node is a major site of accumulation of HIV in the body, as well as being a site where much of the viral replication occurs which leads to the destruction of the body's immune system. To better understand the role of the lymph node in HIV infection and destruction of one s immunity, we wish to examine both the virus itself as well as the effects it is having on various types of white cells (called lymphocytes) obtained simultaneously from both peripheral blood and lymph nodes of people living with HIV (PLWH). We also need to look at cells derived from blood and lymph nodes from people who do not have HIV to serve as a control for experiments. We may also use your lymph node tissue and blood cells to attempt to make new T-cells, or rebuild the immune cells, in the laboratory by adding various factors or other substances released by different cells in the body. If you are living with HIV, you may be asked to undergo a second biopsy six weeks to 12 months after the first biopsy. Because of the ability of aspirin to interfere with blood clotting, you must have refrained from the use of aspirin for one week (7 days) prior to the biopsy date. You also cannot use non-aspirin containing, non-steroidal, anti-inflammatory medications (e.g., ibuprofen, naproxen, and similar drugs) one week (7 days) prior to the biopsy. In addition, pregnancy testing will be performed on all females at the time of admission and a positive test will exclude you from participation. No participant will undergo more than six biopsies while participating in this study unless a particular research requires it.

Conditions

HIV

Study ID

NCT00001316

Start date

Aug 26, 1992

Status verified date

Aug 5, 2026

Eligibility Criteria

Eligibility Criteria

Sex: All

Age: 18 - 70+

Healthy Volunteers: Accepted

  • INCLUSION CRITERIA:

1. HIV status must be documented by a licensed ELISA and confirmed either by Western blot, or plasma viremia.
2. Aged 18 years or older.
3. Ability to give informed, written consent.
4. The following laboratory values:

1. Absolute neutrophil count of greater than 1000/mm\^3
2. PT, PTT, within normal limits, (unless PTT is elevated in presence of positive lupus anticoagulant in a participant with no prior history of abnormal bleeding).
3. Adequate blood counts (PLWH: hemoglobin >= 9.0 g/dL, HCT >= 28%, platelets >= 75,000; participants without HIV: hemoglobin >=11.2 g/dL, HCT >=34.1%, platelets >=150,000)
4. Blood pressure <=180/100; pulse rate 50-100, unless a lower pulse rate is considered normal for the participant
5. Participants who do not have HIV will qualify as control participants.
6. Participants must have a clinically palpable lymph node in an easily accessible location.
7. Willingness to allow blood samples to be used for future studies of HIV infection/pathogenesis, undergo genetic testing including HLA testing, and undergo hepatitis screening

EXCLUSION CRITERIA:

1. Women who are pregnant and/or breast-feeding
2. Currently abusing alcohol or other drugs including narcotics or cocaine
3. Participants with AIDS dementia or with an AIDS related malignancy other than minimal Kaposi's sarcoma.
4. No Aspirin or Non-Steroidal Anti-inflammatory medications (NSIADs) 7 days prior to procedure. Acetaminophen (Tylenol) is permitted at any time.
5. Any medical condition for which the PI feels LN BX might be contraindicated
6. Participants in which sedation is planned. Use of narcotics (other than as prescribed by a physician) or cocaine less than 1 week prior to the date of biopsy will be excluded.

Study Design

Enrollment

400 participants

Anticipated

Interventions and Outcome Measures

Arms

Individuals with HIV

Individuals with HIV

Individuals without HIV

Individuals without HIV

Primary outcome measure

  • Relative burden of HIV [ Time Frame: Throughout ]
  • Immunoregulatory mechanisms [ Time Frame: Throughout ]
  • Effect of Therapy on Viral Burden and Immune Activation [ Time Frame: Throughout ]

Central Contacts and Locations

Central contacts

Catherine A Seamon, R.N.

(301) 402-3481cseamon@cc.nih.gov

Locations

National Institutes of Health Clinical Center

Recruiting

Bethesda, Maryland, United States, 20892

Contacts

For more information at the NIH Clinical Center contact Office of Patient Recruitment (OPR)

800-411-1222ccopr@nih.gov

More Information

Sponsor

National Institute of Allergy and Infectious Diseases (NIAID)

Last update posted

Aug 28, 2026

Last verified

Aug 5, 2026

Keywords

  • Lymph Node
  • Polymerase Chain Reaction (PCR)
  • In Situ Hybridization
  • AIDS
  • Excisional Biopsy
  • Natural History

Trial information was received from ClinicalTrials.gov and was last updated on 2026-09-10. This information was provided to ClinicalTrials.gov by National Institute of Allergy and Infectious Diseases (NIAID) on 2026-08-28.