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The Use of Lymph Node Biopsies to Support HIV Pathogenesis Studies

The Use of Lymph Node Biopsies to Support HIV Pathogenesis Studies

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT01202305
Enrollment
50
Registered
2010-09-15
Start date
2011-04-30
Completion date
2030-04-30
Last updated
2025-04-06

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

HIV

Keywords

HIV, HIV persistence, Lymph node fibrosis

Brief summary

HIV medicines have led to dramatic improvements in health. However, there remains a concern for potential drug toxicities, cost of drugs, and need for life-long treatment. In addition, research has found that health is not completely restored in HIV-infected patients, even if they have been taking effective HIV medicines for a long time. This may be due to direct drug-toxicity, continued replication of the virus, and/or inflammation of the body in response to the virus. Therefore, a more complete understanding of how HIV stays in the body is necessary. Recent research has shown that one of the places that HIV can stay in the body is in lymphatic tissues such as lymph nodes (even in patients who have been taking HIV medicines for a long time). In addition, the amount of damage to the lymphatic tissues can predict how the immune system (CD4+ T cell count) will respond to therapy. The investigators therefore propose a study in which lymph nodes from the groin area will be removed, with the goals of: 1) seeing how much HIV is in lymph nodes and 2) seeing how much damage has happened to the lymph node architecture.

Interventions

Inguinal lymph node biopsy

Sponsors

National Institutes of Health (NIH)
CollaboratorNIH
University of California, San Francisco
Lead SponsorOTHER

Study design

Observational model
CASE_CONTROL
Time perspective
CROSS_SECTIONAL

Eligibility

Sex/Gender
ALL
Age
18 Years to 70 Years
Healthy volunteers
Yes

Inclusion criteria

1. Able to give informed consent 2. No contraindication to surgical procedures 3. Palpable inguinal adenopathy at study entry 4. For HIV seropositive subjects, meeting one of the following criteria: (1) on stable highly active antiretroviral therapy (HAART) with a recent undetectable viral load (\< 50 copies/mL) (HAART suppressed), (2) antiretroviral untreated with an undetectable viral load (\< 50 copies/mL) (elite controllers), or (3) antiretroviral untreated with a detectable viral load (\> 1000 copies/mL) (non-controllers)

Exclusion criteria

1. Known anemia (HIV+ males Hct\<34; females Hct\<32) or contraindication to donating blood 2. Blood coagulation disorder (including bleeding tendency or problems in past with blood clots) 3. Platelets \< 50,000/mm3 4. PTT \> 2x ULN 5. INR \> 1.5 6. Pregnant

Design outcomes

Primary

MeasureTime frame
HIV persistence1 year

Countries

United States

Contacts

Primary ContactRebecca Hoh, RD
Rebecca.Hoh@ucsf.edu415-502-2453

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026