Br J Ophthalmol 1999;83:1186-1189
( October )
Scientific correspondence
Influence of highly active antiretroviral therapy on the
development of CMV disease in HIV positive patients at high risk for
CMV disease
Frank D Verbraaka, René Boomb, Pauline M E Wertheim-van Dillenb, Gerardus J van den Horna, Aize Kijlstraa c, Marc D de Smeta
a Department of
Ophthalmology, Academic Medical Centre, University of Amsterdam,
Amsterdam, Netherlands, b Laboratory of Microbiology, Department of
Virology, Academic Medical Centre, University of Amsterdam, Amsterdam,
Netherlands, c Department of Ophthalmo-Immunology, the
Netherlands Ophthalmic Research Institute, Amsterdam, Netherlands
Correspondence to: Frank D Verbraak,
University of Amsterdam, Academic Medical Centre, Department of
Ophthalmology, Room G2-245, PO Box 22700, 1100 DE Amsterdam,
Netherlands.
Accepted for publication 24 May 1999
BACKGROUND/AIMS
In the
pre-HAART era, HIV positive patients with CD4+ cell counts below 50 cells ×106/l, and those with detectable cytomegalovirus
(CMV) DNA in their peripheral blood, were considered to be at high risk
for the development of CMV disease. With the start of highly active
antiretroviral therapy (HAART), a restoration of immune function
occurred in these patients, and as a consequence patients became less
vulnerable to CMV disease. Since it is not exactly known how HAART
influences CMV viral load in peripheral blood and the incidence of CMV
disease in high risk HIV positive patients a group of patients was
followed before and after initiation of HAART.
METHODS
29 HIV
positive patients, seen in the first 3 months of 1996 at the AIDS
clinic of the Academic Medical Centre, at high risk for development of
CMV disease (positive CMV DNA assay in blood and/or CD4+ cell count
below 50 cells ×106/l), not receiving anti-CMV
maintenance therapy, were included in a prospective cohort study. HAART
was started in the second trimester of 1996. Patients were evaluated
for the occurrence of CMV retinitis, or CMV disease elsewhere,
comparing the incidence of CMV events before and after the start of
HAART. Following the introduction of HAART, CD4+ cell counts and
quantitative polymerase chain reaction (PCR) for CMV DNA in blood were
monitored in all patients who remained alive and were not receiving
anti-CMV maintenance therapy (n=22). Follow up was performed until
August 1998; the mean follow up after the start of HAART was 14.9 months (range 8-22 months).
RESULTS
In the
pre-HAART period four patients developed CMV disease, and four died
(without clinically manifest CMV disease). After the start of HAART no
patient developed CMV disease or died. With HAART, the mean CD4+ cell
counts increased from 34 cells ×106/l to 194 cells
×106/l at the end of follow up. CMV DNA could be detected
in the blood of 11 patients. Quantification showed a decline in the
amount of detectable DNA during follow up. At the last examination only one patient showed a positive PCR assay. This was the only patient with
a CD4+ cell count remaining below 100 cells ×106/l.
CONCLUSION
In HIV
positive patients at high risk of CMV retinitis, either with a positive
CMV PCR assay in blood and/or with CD4+ cell counts below 50 cell
×106/l, HAART causes a dramatic decrease in the
occurrence of CMV disease. This decrease is paralleled by an increase
in CD4+ cell count, and a decrease in the amount of CMV DNA in the
blood, which was below detection levels in all patients with CD4+ cell
counts above 100 cells ×106/l.
© 1999 by British Journal of Ophthalmology