No effect of raltegravir intensification on viral replication markers in the blood of HIV-1–infected patients receiving antiretroviral therapy
RT Gandhi, RW Coombs, ES Chan… - JAIDS Journal of …, 2012 - journals.lww.com
RT Gandhi, RW Coombs, ES Chan, RJ Bosch, L Zheng, DM Margolis, S Read, B Kallungal…
JAIDS Journal of Acquired Immune Deficiency Syndromes, 2012•journals.lww.comBackground: Controversy continues regarding the extent of ongoing viral replication in HIV-1–
infected patients on effective antiretroviral therapy (ART). Adding an additional potent agent,
such as raltegravir, to effective ART in patients with low-level residual viremia may reveal
whether there is ongoing HIV-1 replication. Methods: We previously reported the outcome of
a randomized placebo-controlled study of raltegravir intensification in patients on ART with
HIV-1 RNA< 50 copies per milliliter that showed no effect on residual viremia measured by …
infected patients on effective antiretroviral therapy (ART). Adding an additional potent agent,
such as raltegravir, to effective ART in patients with low-level residual viremia may reveal
whether there is ongoing HIV-1 replication. Methods: We previously reported the outcome of
a randomized placebo-controlled study of raltegravir intensification in patients on ART with
HIV-1 RNA< 50 copies per milliliter that showed no effect on residual viremia measured by …
Background: Controversy continues regarding the extent of ongoing viral replication in HIV-1–infected patients on effective antiretroviral therapy (ART). Adding an additional potent agent, such as raltegravir, to effective ART in patients with low-level residual viremia may reveal whether there is ongoing HIV-1 replication.
Methods: We previously reported the outcome of a randomized placebo-controlled study of raltegravir intensification in patients on ART with HIV-1 RNA< 50 copies per milliliter that showed no effect on residual viremia measured by single copy assay. We now report the effects of raltegravir intensification in that trial on other potential measures of ongoing HIV-1 replication as follows: 2-LTR HIV-1 circles, total cellular HIV-1 DNA, and T-cell activation.
Results: Of 50 patients tested, 12 (24%) had 2-LTR circles detected at baseline. Patients who were 2-LTR–positive had higher plasma HIV-1 RNA and HIV-1 DNA levels than 2-LTR–negative individuals. At week 12 of raltegravir intensification, there was no change from baseline in 2-LTR circles, in total HIV-1 DNA or in the ratio of 2-LTR circles to total HIV-1 DNA. There was also no change in markers of T-cell activation.
Conclusions: In HIV-1–infected individuals on effective ART, we find no evidence of ongoing viral replication in the blood that is suppressible by raltegravir intensification. The results imply that raltegravir intensification alone will not eradicate HIV-1 infection.
Lippincott Williams & Wilkins