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OpenTrials
Completed

NCT Number: NCT00000852

A Pilot Study of Allogeneic Lymphocyte Transfer in HIV Infection

To examine, in HIV-infected patients, the safety of allogeneic lymphocyte transfer (i.e., infusion of white blood cells taken from an HIV-negative parent, sibling, or adult offspring who has a compatible blood type). To measure the distribution and survival of allogeneic lymphocytes in the circulation of HIV-infected patients, and to determine whether their infusion results in enhanced immunity. To determine whether enhanced immunity is passively transferred or actively induced.

There is evidence that periodic infusion of allogeneic lymphocytes obtained from the peripheral blood of HLA-matched HIV-1 seronegative siblings of patients with AIDS can, in some instances, restore the number of circulating CD4+ lymphocytes. However, more controlled studies are needed to better quantitate the immunologic reconstitution seen with this type of therapy.

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Key information

Age range

18 year–50 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Univ Hosp of Cleveland / Case Western Reserve Univ

Cleveland, Ohio, 44106, United States

About this study

There is evidence that periodic infusion of allogeneic lymphocytes obtained from the peripheral blood of HLA-matched HIV-1 seronegative siblings of patients with AIDS can, in some instances, restore the number of circulating CD4+ lymphocytes. However, more controlled studies are needed to better quantitate the immunologic reconstitution seen with this type of therapy.

Lymphocytes obtained by leukapheresis from a healthy, HIV-negative parent, sibling, or adult offspring of the HIV-infected patient are infused at day 0 and at weeks 4 and 8. A small portion of the lymphocytes obtained at day 0 will be radiolabeled prior to infusion, and two total body scans will be performed. Patients also undergo two tonsillar biopsies. Patients are followed weekly for 16 weeks, then by telephone periodically for 3 years (at 1 year, 2 years, 2.5 years, and 3 years).

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

Concurrent Medication:

Required:

  • Stable antiretroviral therapy.

Allowed:

  • Maintenance therapy for a controlled opportunistic infection.

Patients must have:

  • HIV infection.
  • CD4 count 50-200 cells/mm3.
  • No ongoing major opportunistic infections.
  • Been on stable antiretroviral therapy for the past 2 months.
  • Tonsils present.
  • Life expectancy greater than 6 months.
  • An HLA-single haplotype matched, single haplotype mismatched parent, sibling, or adult offspring who is ABO, Rh compatible to serve as an HIV-negative lymphocyte donor.

Exclusion criteria

Co-existing Condition:

Patients with the following symptoms or conditions are excluded:

  • Lymphoma or other malignancy requiring chemotherapy.
  • Bleeding disorder that would preclude a tonsillar biopsy.
  • Antibody on donor/recipient lymphocyte reactive antibody assay.

Donors with the following symptoms or conditions are excluded:

  • Medical condition that would endanger health of donor or recipient.
  • Failure to meet established donor standards on blood screening tests.
  • CMV seropositivity if the patient (recipient) is CMV seronegative.
  • Pregnancy.

Concurrent Medication:

Excluded:

  • GM-CSF or G-CSF.
  • Any investigational drug.
  • Immunomodulators (such as interferon, steroids, topical corticosteroids, thalidomide, pentoxifylline, IL-2).
  • Nonsteroidal anti-inflammatory drugs.
  • Aspirin.

Prior Treatment:

Excluded:

  • Blood transfusion within the past 2 months.

Required:

  • Stable antiretroviral therapy for at least 2 months prior to study entry.

Active substance abuse.

Treatment and study plan

Allogeneic lymphocyte transfer

Procedure

Sponsors and collaborators

Lead sponsor

National Institute of Allergy and Infectious Diseases (NIAID)

Nih

Registry information

Important dates

First posted
Aug 31, 2001
Registry last updated
Jun 24, 2005

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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