Literature DB >> 11090360

Control of SIV rebound through structured treatment interruptions during early infection.

F Lori1, M G Lewis, J Xu, G Varga, D E Zinn, C Crabbs, W Wagner, J Greenhouse, P Silvera, J Yalley-Ogunro, C Tinelli, J Lisziewicz.   

Abstract

In a randomized controlled trial with acute simian immunodeficiency virus (SIV)-infected macaques, both highly active antiretroviral therapy (HAART) and HAART with fixed-schedule structured treatment interruption (STI-HAART; alternating 3 weeks on and 3 weeks off therapy) suppressed viral load. In the STI-HAART group, T cell virus-specific immune response (VIR) and control of viral rebound increased concurrently during subsequent interruptions. In contrast, VIR did not increase and SIV rebounded after permanent treatment withdrawal in all animals on continuous HAART. Fixed-schedule STI-HAART appears to be an effective alternative to continuous HAART for the early treatment of retroviral infection.

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Year:  2000        PMID: 11090360     DOI: 10.1126/science.290.5496.1591

Source DB:  PubMed          Journal:  Science        ISSN: 0036-8075            Impact factor:   47.728


  34 in total

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9.  CD8+-cell-mediated suppression of virulent simian immunodeficiency virus during tenofovir treatment.

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