The clinical benefit of highly active antiretroviral therapy (HAART) has be
en attributed to its suppression of viral replication and improvement in th
e CD4 lymphocyte count. However, the development of clinical symptoms secon
dary to previously silent opportunistic pathogens shortly after beginning H
AART has been reported as a distinct clinical syndrome and seems to be asso
ciated with inflammatory phenomena surrounding a rapid restoration of the i
mmune system in previously immunosuppressed patients. Herein, we report nin
e (3.6%) episodes of opportunistic infections (01) in 247 human immunodefic
iency virus (HIV)-infected patients undergoing HAART in a reference HIV/AID
S institution located in Madrid, Spain. In all instances, 01 clustered with
in the first 3 months after beginning HAART Episodes of cerebral toxoplasmo
sis (three cases), Pneumocystis carinii pneumonia (two eases), and herpes t
ester (two cases) occurred in persons without a previous AIDS-defining illn
ess, in addition a relapse of cytomegalovirus retinitis and a rebound in Ka
posi's sarcoma were seen, respectively. in another two patients. Four of th
e nine subjects had a CD4 count above 200 cells/mm(3) before HAART began. O
f these, one developed Pneumocystis pneumonia and one other cerebral toxopl
asmosis. In conclusion, prophylaxis and close clinical monitoring of HIV-in
fected patients should be considered for the first 3 months after beginning
HAART, even for subjects without severe immunosuppression.