ART suppresses plasma HIV-1 RNA to a stable set point predicted by pretherapy viremia

被引:280
作者
Maldarelli, Frank [1 ]
Palmer, Sarah
King, Martin S.
Wiegand, Ann
Polis, Michael A.
Mican, JoAnn
Kovacs, Joseph A.
Davey, Richard T.
Rock-Kress, Diane
Dewar, Robin
Liu, Shuying
Metcalf, Julia A.
Rehm, Catherine
Brun, Scott C.
Hanna, George J.
Kempf, Dale J.
Coffin, John M.
Mellors, John W.
机构
[1] HIV Drug Resistance Program, NCI, Frederick, MD USA
[2] Abbott Labs, Global Pharmaceut Res & Dev, Abbott Pk, IL USA
[3] Nalt Inst Allergy & Infect Dis, Lab Immunoregulat, NIH, Bethesda, MD USA
[4] Natl Inst Hlth Clin Ctr, Dept Crit Care, NIH, Bethesda, MD USA
[5] SAIC Frederick, Frederick, MD USA
[6] Univ Pittsburgh, Ctr Med, Div Infect Dis, Pittsburgh, PA USA
关键词
D O I
10.1371/journal.ppat.0030046
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Current antiretroviral therapy is effective in suppressing but not eliminating HIV-1 infection. Understanding the source of viral persistence is essential for developing strategies to eradicate HIV-1 infection. We therefore investigated the level of plasma HIV-1 RNA in patients with viremia suppressed to less than 50-75 copies/ml on standard protease inhibitor- or non-nucleoside reverse transcriptase inhibitor-containing antiretroviral therapy using a new, real-time PCR-based assay for HIV-1 RNA with a limit of detection of one copy of HIV-1 RNA. Single copy assay results revealed that > 80% of patients on initial antiretroviral therapy for 60 wk had persistent viremia of one copy/ml or more with an overall median of 3.1 copies/ml. The level of viremia correlated with pretherapy plasma HIV-1 RNA but not with the specific treatment regimen. Longitudinal studies revealed no significant decline in the level of viremia between 60 and 110 wk of suppressive antiretroviral therapy. These data suggest that the persistent viremia on current antiretroviral therapy is derived, at least in part, from long-lived cells that are infected prior to initiation of therapy.
引用
收藏
页码:484 / 488
页数:5
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