Substantial correlation between HIV type 1 drug-associated resistance mutations in plasma and peripheral blood mononuclear cells in treatment-experienced patients

被引:38
作者
Devereux, HL
Loveday, C
Youle, M
Sabin, CA
Burke, A
Johnson, M
机构
[1] UCL Royal Free & Univ Coll, Sch Med, Dept Retrovirol, London NW3 2PF, England
[2] UCL Royal Free & Univ Coll, Sch Med, Royal Free Ctr HIV Med, London NW3 2PF, England
[3] UCL Royal Free & Univ Coll, Sch Med, Dept Primary Care & Populat Sci, London NW3 2PF, England
关键词
D O I
10.1089/08892220050075273
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
The correlation of detectable HIV-1 drug resistance mutations in plasma and PBMCs in patients extensively treated with all antiretroviral drug classes has not been fully elucidated. The detection of mutations in PBMCs may reveal resistant HIV-1 associated with past therapies. In addition, these measures in PBMCs may have a practical value when plasma virus is at low levels that are difficult to detect with current assays. The reverse transcriptase (RT) and protease (P) genes were analyzed for drug resistance, using an in-house method carried out on 36 paired samples of plasma and PBMCs from 12 treatment-experienced patients in order to investigate resistance in the two compartments. When viruses in plasma and PBMCs were analyzed by patient, the mean of the Cohen kappa values was 0.728 (substantial agreement). When viruses were analyzed by codon the mean of the Cohen kappa values was 0.715 (substantial agreement). Baseline samples were concordant at 280 of 288 (97%) codons analyzed. This study shows that a minority of mutations associated with previous therapy can be detected in PBMCs and not in plasma. Overall, mutations in plasma and PBMCs showed a substantial correlation in extensively treated patients, suggesting that either compartment is suitable for the detection of mutations as a virological guide for clinical care.
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页码:1025 / 1030
页数:6
相关论文
共 13 条
[1]  
BAXTER JD, 1999, 6 C RETR OPP INF CHI
[2]  
Devereux HL, 1999, AIDS, V13, pF123, DOI 10.1097/00002030-199912240-00001
[3]  
DURANT J, 1998, 4 INT C DRUG THER HI
[4]  
Günthard HF, 1998, J VIROL, V72, P2422
[5]  
HIGUCHI R, 1989, PCR TECHNOLOGY
[6]   Antiretroviral drug resistance testing in adults with HIV infection -: Implications for clinical management [J].
Hirsch, MS ;
Conway, B ;
D'Aquila, RT ;
Johnson, VA ;
Brun-Vézinet, F ;
Clotet, B ;
Demeter, LM ;
Hammer, SM ;
Jacobsen, DM ;
Kuritzkes, DR ;
Loveday, C ;
Mellors, JW ;
Vella, S ;
Richman, DD .
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 1998, 279 (24) :1984-1991
[7]   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
[8]   THE APPEARANCE OF DRUG RESISTANCE-ASSOCIATED POINT MUTATIONS IN HIV TYPE-1 PLASMA RNA PRECEDES THEIR APPEARANCE IN PROVIRAL DNA [J].
KAYE, S ;
COMBER, E ;
TENANTFLOWERS, M ;
LOVEDAY, C .
AIDS RESEARCH AND HUMAN RETROVIRUSES, 1995, 11 (10) :1221-1225
[9]   Comparison of human immunodeficiency virus type 1 (HIV-1) protease mutations in HIV-1 genomes detected in plasma and in peripheral blood mononuclear cells from patients receiving combination drug therapy [J].
Koch, N ;
Yahi, N ;
Ariasi, F ;
Fantini, J ;
Tamalet, C .
JOURNAL OF CLINICAL MICROBIOLOGY, 1999, 37 (05) :1595-1597
[10]   MEASUREMENT OF OBSERVER AGREEMENT FOR CATEGORICAL DATA [J].
LANDIS, JR ;
KOCH, GG .
BIOMETRICS, 1977, 33 (01) :159-174