The thymus is the primary site of T cell ontogeny and selection during
fetal and neonatal development. Previous studies have established tha
t the thymus is also a site of HIV-1 Infection, as early as the first
trimester of pregnancy. Alteration of the thymocyte maturation process
by HIV-1 could impact on the peripheral T cell population and interfe
re with immune responses. A neonatal thymic organ culture system was e
stablished to study HIV-1 Infection within the thymus. We have shown t
hat this primary tissue isolate can support a productive HIV-1 infecti
on. Infection occurred without detectable thymocyte cytopathology. The
ability to infect the developing thymocyte within an intact micro env
ironment will enable us to further establish the kinetics of acute HIV
-1 thymic infection and its consequences on lymphocyte maturation.