Virological effectiveness and CD4+ T-cell increase over early and late courses in HIV infected patients on antiretroviral therapy: focus on HCV and anchor class received

<p>Abstract</p> <p>Background</p> <p>The aim of this study was to explore the effects of HCV co-infection on virological effectiveness and on CD4+ T-cell recovery in patients with an early and sustained virological response after HAART.</p> <p>Methods</p&...

Full description

Bibliographic Details
Main Authors: Motta Davide, Brianese Nigritella, Focà Emanuele, Nasta Paola, Maggiolo Franco, Fabbiani Massimiliano, Cologni Giuliana, Di Giambenedetto Simona, Di Pietro Massimo, Ladisa Nicoletta, Sighinolfi Laura, Costarelli Silvia, Castelnuovo Filippo, Torti Carlo
Format: Article
Language:English
Published: BMC 2012-06-01
Series:AIDS Research and Therapy
Subjects:
Online Access:http://www.aidsrestherapy.com/content/9/1/18
Description
Summary:<p>Abstract</p> <p>Background</p> <p>The aim of this study was to explore the effects of HCV co-infection on virological effectiveness and on CD4+ T-cell recovery in patients with an early and sustained virological response after HAART.</p> <p>Methods</p> <p>We performed a longitudinal analysis of 3,262 patients from the MASTER cohort, who started HAART from 2000 to 2008. Patients were stratified into 6 groups by HCV status and type of anchor class. The early virological outcome was the achievement of HIV RNA <500 copies/ml 4–8 months after HAART initiation. Time to virological response was also evaluated by Kaplan-Meier analysis. The main outcome measure of early immunological response was the achievement of CD4+ T-cell increase by ≥100/mm<sup>3</sup> from baseline to month 4–8 in virological responder patients. Late immunological outcome was absolute variation of CD4+ T-cell count with respect to baseline up to month 24. Multivariable analysis (ANCOVA) investigated predictors for this outcome.</p> <p>Results</p> <p>The early virological response was higher in HCV Ab-negative than HCV Ab-positive patients prescribed PI/r (92.2% <it>versus</it> 88%; <it>p</it> = 0.01) or NNRTI (88.5% <it>versus</it> 84.7%; <it>p</it> = 0.06). HCV Ab-positive serostatus was a significant predictor of a delayed virological suppression independently from other variables, including types of anchor class. Reactivity for HCV antibodies was associated with a lower probability of obtaining ≥100/mm<sup>3</sup> CD4+ increase within 8 months from HAART initiation in patients treated with PI/r (62.2% among HCV Ab-positive patients <it>versus</it> 70.9% among HCV Ab-negative patients; <it>p</it> = 0.003) and NNRTI (63.7% <it>versus</it> 74.7%; <it>p</it> < 0.001). Regarding late CD4+ increase, positive HCV Ab appeared to impair immune reconstitution in terms of absolute CD4+ T-cell count increase both in patients treated with PI/r (<it>p</it> = 0.013) and in those treated with NNRTI (<it>p</it> = 0.002). This was confirmed at a multivariable analysis up to 12 months of follow-up.</p> <p>Conclusions</p> <p>In this large cohort, HCV Ab reactivity was associated with an inferior virological outcome and an independent association between HCV Ab-positivity and smaller CD4+ increase was evident up to 12 months of follow-up. Although the difference in CD4+ T-cell count was modest, a stricter follow-up and optimization of HAART strategy appear to be important in HIV patients co-infected by HCV. Moreover, our data support anti-HCV treatment leading to HCV eradication as a means to facilitate the achievement of the viro-immunological goals of HAART.</p>
ISSN:1742-6405