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Influence of Blips of Viral Load during HAART on Control of Viral Replication after Discontinuing HAART
Pedro Castro*, A López, M Plana, C Gil, R González, A Vilella, E Fumero, T Pumarola, J Gatell, and F García
Hosp Clin, Univ of Barcelona, Spain
Background: Data
conflict concerning the effects on HIV-1 infection of transient increases of
plasma viral load (PVL) (“blips”). It has been proposed that patients with
blips could risk poorer outcome. Some retrospective studies suggest an
association of blips with an increase in HIV-specific immune responses, which
might help to improve the viral control after HAART interruption. The objective
of the present study is to address prospectively in a cohort of treated
patients the influence of blips on viral rebound after HAART discontinuation.
Methods: We
studied blips in 26 patients included in a single-center
prospective, randomized, double blind, placebo-controlled clinical trial to
evaluate the effect of a vaccination program on PVL in successfully treated
HIV-infected adults. We did not observe that vaccinated patients had a higher
proportion of blips than control patients. Patients were on HAART as long as 2
months after the last immunization and HAART was discontinued afterward (month
12) for at least 6 months (month 18). Blood samples were taken every month from
0 to 18. VL and CD4+ T cells were analyzed. We compared PVL rebounds
in the group of patients who had blips with the group where blips were not
detected.
Results:
We found
transient elevation of viral load >200 copies/mL
in 9 of 26 patients and in 21 of 312 viral load determinations. The blips group
had a higher PVL rebound (area under the curve of 2.22 vs
1.61, p = 0.009; peak viral load 5,28 vs 4,67 log, p = 0.018) than the no-blips group. The
drop in percentage of CD4 T cells after HAART discontinuation was similar in
both groups (11% vs 13%, blips vs
no-blips, respectively, p = 0.55).
However, the blips group had significantly lower CD4+ T-cell counts
at study entry (month 0) (34 vs 41%
; blips vs no-blips group, respectively, p = 0.04). On the other hand,
differences in PVL rebound and drop in CD4+ T cells after HAART
interruption between vaccinated and not vaccinated were not observed.
Conclusions: Early
stage HAART-treated patients with blips controlled viral replication after
interruption of treatment more poorly, although it did not influence the drop
in CD4+ T cells after 6 months off HAART. Repeated immunological
stimuli with commercial vaccines (a total of 195 stimuli in 13 patients) do not
influence in the rebound after stopping HAART.
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