The decay of HIV and turnover of CD4+ lymphocytes have been described recently as being very rapid suggesting that HIV replication is highly productive and that the turnover of CD4+ cells is high. This application is to extend these observations.
Specific Aim 1 is to define the kinetics of decay of HIV or SIV in the compartments containing HIV by using antiviral agents.
The Second Aim i s to define where SIV is cleared and produced in macaques.
The Third Aim i s to characterize the types of lymphocytes before and after antivirals and to determine the mechanism of their regeneration.
The Fourth Aim i s to compare populations of HIV+ people for lymphocyte subpopulations by examining the telomeric length in sequential samples of CD4+ and CD8+ lymphocytes. The Fifth Aim is to examine CD4 and CD8 lymphocytic tissue/turnover using BrdU studies in monkeys with or without SIV infection.
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