Quantitation of HTLV-I proviral load by a TaqMan real-time PCR assay

被引:107
|
作者
Dehée, A
Césaire, R [1 ]
Désiré, N
Lézin, A
Bourdonné, O
Béra, O
Plumelle, Y
Smadja, D
Nicolas, JC
机构
[1] Ctr Hosp & Univ Ft de France, Lab Virol Immunol, F-97261 Fort De France, Martinique, France
[2] Hop Rothschild, Microbiol Lab, F-75571 Paris, France
[3] Ctr Hosp & Univ Ft de France, Hematol Lab, F-97261 Fort De France, Martinique, France
[4] Ctr Hosp & Univ Ft de France, Neurol Serv, F-97261 Fort De France, Martinique, France
关键词
HTLV-I; real-time quantitative PCR; TaqMan;
D O I
10.1016/S0166-0934(01)00445-1
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
A quantitative real-time PCR assay was developed to measure the proviral load of human T-lymphotropic virus type I (HTLV-I) in peripheral blood mononuclear cells (PBMCs). The HTLV-I copy number was referred to the actual amount of cellular DNA by means of the quantitation of the albumin gene. Ten copies of HTLV-I DNA could be detected with 100%,, sensitivity, and the assay had a wide range of at least 5 log,,. Intra- and inter-assay reproducibility was evaluated using independent extractions of PBMCs from an HTLV-I-infected patient (coefficients of variation, 24 and 7% respectively). The performance of this TaqMan PCR assay, coupled with its high throughput, thus allows reliable routine follow-up of HTLV-I proviral load in infected patients. Preliminary results using clinical samples indicate a higher proviral load in patients with HTLV-I-associated myelopathy/tropical spastic paraparesis than in asymptomatic carriers, and also suggest the usefulness of this quantitative measurement to assess the etiological link between HTLV-I and adult T-cell leukaemia/lymphoma-like syndromes. (C) 2002 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:37 / 51
页数:15
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