HIV Infections Clinical Trial
Official title:
Intensification of HIV-Specific CD4 and CD8 Activity by Cycling Highly Active Antiretroviral Therapy (HAART) in Pediatric/Adolescent Patients With Less Than 50 HIV RNA Copies/ml
Some patients taking anti-HIV drugs as part of highly active antiretroviral therapy (HAART) do not show any HIV in the blood; however, some HIV will remain hidden in the body and, if the drugs are stopped, will return to the blood. The purpose of this study is to determine if short periods of stopping HAART increase the activity of CD8 and CD4 cells (cells of the immune system that fight infection), if repeated stopping of these drugs for longer periods of time and restarting them will increase effectiveness of HAART, and if the increased immune system activity as a result of stopping treatment leads to lower levels of HIV over time.
Some HIV infected patients taking HAART have been able to achieve prolonged suppression of
HIV viral load for extended periods of time. However, discontinuing HAART has consistently
resulted in HIV's return to plasma. Both CD8 and CD4 cells are markedly reduced in
individuals with prolonged HIV suppression; control of and response to cell-associated HIV
is dependent on immune-mediated mechanisms involving these cells. It is hypothesized that a
brief and low-level increase in HIV levels resulting from HAART interruption might boost
HIV-specific CD8 and CD4 T-cell counts. After suppression of viral load with the
reintroduction of HAART, the expanded CD8 population might be able to better control viral
replication and better respond to cell-associated HIV. Future treatment interruption may
lead to longer periods of undetectable viral loads.
Patients are divided into 2 age cohorts, with Cohort 1 consisting of children and
adolescents 4 years and older up to 21 years of age, and Cohort 2 consisting of children and
adolescents 2 years and older up to 4 years of age. Patients will be assigned to one of 2
groups. Group A patients will participate in drug holiday cycles from HAART and then back to
HAART; Group B is a control group that remains on continuous HAART throughout the study.
Cycle 1 for Group A patients begins with 18 days of HAART and a 3-day drug holiday. At the
end of the drug holiday, viral load is measured and HAART is resumed for 28 days (detectable
virus cycle) if viral load is detectable after the drug holiday. If viral load remains below
the level of detection, the patient begins the next drug holiday cycle. With each subsequent
drug holiday cycle, time off HAART will increase by 2 days. Patients failing 4 repeated
detectable virus (28-day treatment) cycles will be taken off study.
Patients will be enrolled in this study for a minimum of 142 weeks. For Group A, HIV viral
load and CD4 cell count are measured at the end of each drug holiday and each HAART
resumption; HIV-specific CD4 and CD8 responses are measured every 3 cycles; and
cell-associated HIV is assessed at entry, at 12-week intervals, and at the end of the study.
For Group B, physical exams are conducted and HIV viral load and other blood work are
measured every 12 weeks.
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