Wl. Drew et al., FAILURE OF HIGH-DOSE ORAL ACYCLOVIR TO SUPPRESS CMV VIRURIA OR INDUCEGANCICLOVIR-RESISTANT CMV IN HIV ANTIBODY-POSITIVE PATIENTS, Journal of acquired immune deficiency syndromes and human retrovirology, 8(3), 1995, pp. 289-291
Ninety-three symptomatic HIV antibody positive patients were randomize
d to receive zidovudine (ZDV) 600 mg/day and acyclovir (ACV) 4,800 mg
orally per day versus ZDV 600 mg/day plus placebo. Urine was obtained
at 3-month intervals and cultured for cytomegalovirus (CMV) in diploid
fibroblast cells. The percent of urine specimens positive for CMV was
7.1% in the ZDV group and 5.8% in the ZDV plus ACV group (p = 0.55);
27% of patients had at least one urine culture positive for CMV while
taking ZDV, versus 20% of patients taking the combination of ZDV plus
ACV (p = 0.52). We conclude that ACV at a dosage of 4,800 mg/day does
not suppress CMV excretion in urine of symptomatic HIV antibody positi
ve patients taking concurrent ZDV. Use of ACV did not appear to induce
resistance of CMV to ganciclovir since the ID50 of isolates from the
two treatment groups did not differ.