Immune reconstitution in the first year of potent antiretroviral therapy and its relationship to virologic response.
E Connick, M M Lederman, B L Kotzin...
https://pubmed.ncbi.nlm.nih.gov/10608789Completed
Led by National Institute of Allergy and Infectious Diseases (NIAID) · Updated on 2021-11-04
55
Participants Needed
3
Research Sites
N/A
Total Duration
To determine whether administration of a highly active antiretroviral treatment regimen consisting of ritonavir (ABT-538), zidovudine (AZT), and lamivudine (3TC) is associated with the restoration of delayed type hypersensitivity and lymphocyte proliferative responses in patients with moderately advanced HIV-1 infection. To better characterize in these patients the phenotype of the expanded lymphocyte subpopulations, as well as the genotype, phenotype, and cellular origin of viruses that persist after initiation of therapy, and the genotype and phenotype of drug-resistant isolates that emerge during therapy. Although plasma viral load drops dramatically after initiation of powerful antiretrovirals, it does not drop to zero. It appears that a new steady state is reached, suggesting that a reservoir may exist of virus-producing cells, possibly cells of monocyte/macrophage lineage, that continue to produce a low level of virus despite antiretroviral treatment.
CONDITIONS
The Effectiveness of Ritonavir Plus Zidovudine Plus Lamivudine in HIV-Infected Patients
You may qualify if you...
Inclusion Criteria
Concurrent Medication:
Allowed:
Concurrent Treatment:
Allowed:
Patients must have:
Prior Medication:
Required:
Allowed:
Exclusion Criteria
Co-existing Condition:
Patients with the following symptoms or conditions are excluded:
Concurrent Medication:
Excluded:
[AS PER AMENDMENT 8/27/96: Immunization must be avoided during the antiretroviral washout period.]
Patients with the following prior conditions are excluded:
Prior Medication:
Excluded:
[AS PER AMENDMENT 8/27/96: Immunization must be avoided prior to the antiretroviral washout period.]
Active substance abuse.
You will not qualify if you...
History of severe allergic reactions to study medication Currently pregnant or breastfeeding Recent participation in another clinical trial within the last 30 days Presence of uncontrolled medical conditions that could affect safety
Total: 3 locations
1
University of Colorado Hospital CRS
Aurora, Colorado, United States, 80045
Status Unknown
2
Rush Univ. Med. Ctr. ACTG CRS
Chicago, Illinois, United States, 60612
Status Unknown
3
Case CRS
Cleveland, Ohio, United States, 44106
Status Unknown
Study Type
INTERVENTIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
TREATMENT
Number of Arms
0
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