Few modifications of the Cobas Amplicor HIV Monitor 1.5 test allow reliable quantitation of HIV-1 proviral load in peripheral blood mononuclear cells

被引:18
作者
Lillo, FB
Grasso, MA
Lodini, S
Bellotti, MG
Colucci, G
机构
[1] Hosp San Raffaele, IRCCS, Virol Lab, AIDS Ctr San Luigi, I-20127 Milan, Italy
[2] RIC, Roche Mol Syst, CH-6343 Rotkreuz, Switzerland
[3] Roche Diagnost Syst SpA, I-20052 Monza, Italy
关键词
HIV-DNA; HAART monitoring; CAHIM;
D O I
10.1016/j.jviromet.2004.05.008
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Recent studies have suggested that monitoring the amount of HIV provirus in peripheral blood mononuclear cells (PBMCs) may be a useful end point for HAART where, in combination with plasma viral load, it provides additional information as to the possibility of virus eradication. In the present study, a modified version of the Cobas Amplicor HIV-1 Monitor test (CAHIM), currently used to quantify plasma viremia, have been evaluated to also measure the amount of proviral DNA in PBMCs. The analytical and clinical performance of the modified CAHIM test was assessed by quantifying different amounts of a standard HIV-DNA preparation obtained from the 8E5 cell line and by analysing 165 patients and controls samples. In these experiments, the modified test, that showed a linear dynamic range from 1.7 to 4.7 log(10) copies/10(6) cells (r = 0.99) with a maximum CV of 20%, proved able to detect and quantify HIV-DNA in all but one clinical samples, with concentrations varying from 1.3 to 3.8 log(10) copies/10(6) cells. During anti-retroviral treatment, the assay revealed different proviral DNA time courses associated with viral load changes and inversely correlated with CD4+ cells count. As expected, HIV-DNA was always detectable even when plasma viremia fell below the CAHIM cut-off. The modified CAHIM test specificity was confirmed by testing 20 HIV-negative samples in triplicates. Taken together, the data showed that the modified CAHIM test can be used to monitor HIV proviral DNA changes during HAART and can help in investigating further the clinical use of this marker. (C) 2004 Elsevier B.V. All rights reserved.
引用
收藏
页码:201 / 205
页数:5
相关论文
共 16 条
[1]   EARLY DIAGNOSIS OF HUMAN-IMMUNODEFICIENCY-VIRUS INFECTION IN CHILDREN LESS-THAN MONTHS OF AGE - COMPARISON OF POLYMERASE CHAIN-REACTION, CULTURE, AND PLASMA ANTIGEN CAPTURE TECHNIQUES [J].
BORKOWSKY, W ;
KRASINSKI, K ;
POLLACK, H ;
HOOVER, W ;
KAUL, A ;
ILMETMOORE, T .
JOURNAL OF INFECTIOUS DISEASES, 1992, 166 (03) :616-619
[2]   PCR-based assay to quantify human immunodeficiency virus type 1 DNA in peripheral blood mononuclear cells [J].
Christopherson, C ;
Kidane, Y ;
Conway, B ;
Krowka, J ;
Sheppard, H ;
Kwok, S .
JOURNAL OF CLINICAL MICROBIOLOGY, 2000, 38 (02) :630-634
[3]   Relationship between the size of the human immunodeficiency virus type 1 (HIV-1) reservoir in peripheral blood CD4+ T cells and CD4+:CD8+ T cell ratios in aviremic HIV-1-Infected individuals receiving long-term highly active antiretroviral therapy [J].
Chun, TW ;
Justement, JS ;
Pandya, P ;
Hallahan, CW ;
McLaughlin, M ;
Liu, SY ;
Ehler, LA ;
Kovacs, C ;
Fauci, AS .
JOURNAL OF INFECTIOUS DISEASES, 2002, 185 (11) :1672-1676
[4]   Presence of an inducible HIV-1 latent reservoir during highly active antiretroviral therapy [J].
Chun, TW ;
Stuyver, L ;
Mizell, SB ;
Ehler, LA ;
Mican, JAM ;
Baseler, M ;
Lloyd, AL ;
Nowak, MA ;
Fauci, AS .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1997, 94 (24) :13193-13197
[5]  
DONADULA G, 2001, JID, V183, P1682
[6]   Identification of a reservoir for HIV-1 in patients on highly active antiretroviral therapy [J].
Finzi, D ;
Hermankova, M ;
Pierson, T ;
Carruth, LM ;
Buck, C ;
Chaisson, RE ;
Quinn, TC ;
Chadwick, K ;
Margolick, J ;
Brookmeyer, R ;
Gallant, J ;
Markowitz, M ;
Ho, DD ;
Richman, DD ;
Siliciano, RF .
SCIENCE, 1997, 278 (5341) :1295-1300
[7]   BIOLOGICAL AND BIOCHEMICAL-CHARACTERIZATION OF A CLONED LEU-3- CELL SURVIVING INFECTION WITH THE ACQUIRED-IMMUNE-DEFICIENCY-SYNDROME RETROVIRUS [J].
FOLKS, TM ;
POWELL, D ;
LIGHTFOOTE, M ;
KOENIG, S ;
FAUCI, AS ;
BENN, S ;
RABSON, A ;
DAUGHERTY, D ;
GENDELMAN, HE ;
HOGGAN, MD ;
VENKATESAN, S ;
MARTIN, MA .
JOURNAL OF EXPERIMENTAL MEDICINE, 1986, 164 (01) :280-290
[8]   Cell-associated HIV-1-DNA quantitation after highly active antiretroviral therapy-treated primary infection in patients with persistently undetectable plasma HIV-1 RNA [J].
Garrigue, I ;
Pellegrin, I ;
Hoen, B ;
Dumon, B ;
Harzic, M ;
Schrive, MH ;
Séréni, D ;
Fleury, H .
AIDS, 2000, 14 (18) :2851-2855
[9]   QUANTITATION OF HUMAN-IMMUNODEFICIENCY-VIRUS TYPE-1 DNA AND RNA BY A NOVEL INTERNALLY CONTROLLED PCR ASSAY [J].
GUPTA, P ;
DING, M ;
COTTRILL, M ;
RINALDO, C ;
KINGSLEY, L ;
WOLINSKY, S ;
MELLORS, J .
JOURNAL OF CLINICAL MICROBIOLOGY, 1995, 33 (06) :1670-1673
[10]   RAPID TURNOVER OF PLASMA VIRIONS AND CD4 LYMPHOCYTES IN HIV-1 INFECTION [J].
HO, DD ;
NEUMANN, AU ;
PERELSON, AS ;
CHEN, W ;
LEONARD, JM ;
MARKOWITZ, M .
NATURE, 1995, 373 (6510) :123-126