A key question in understanding the status of the immune system in HIV-I in
fection is whether the adult thymus contributes to reconstitution of periph
eral T lymphocytes. We analyzed the thymus in adult patients who died of HI
V-1 infection. In addition, we studied the clinical course of HIV-1 infecti
on in three patients thymectomized for myasthenia gravis and determined the
effect of antiretroviral therapy on CD4(+) T cells. We found that five of
seven patients had thymus tissue at autopsy and that all thymuses identifie
d had inflammatory infiltrates surrounding lymphodepleted thymic epithelium
. Two of seven patients also had areas of thymopoiesis; one of these patien
ts had peripheral blood CD4(+) T-cell levels of <50/mm(3) for 51 months pri
or to death. Of three thymectomized patients, one rapidly progressed to AID
S, one progressed to AIDS over seven years (normal progressor), whereas the
third remains asymptomatic at least seven years after seroconversion. Both
latter patients had rises in peripheral blood CD4(+) T cells after antiret
roviral therapy Most patients who died of complications of HIV-1 infection
did not have functional thymus tissue, and when present, thymopoiesis did n
ot prevent prolonged lymphopenia. Thymectomy before HIV-1 infection did not
preclude either peripheral CD4(+) T-cell rises or clinical responses after
antiretroviral therapy.