Effects of drug resistance on viral load in patients failing antiretroviral therapy

被引:26
作者
Machouf, N
Thomas, R
Nguyen, VK
Trottier, B
Boulassel, MR
Wainberg, MA
Routy, JP
机构
[1] Clin Med Actuel, Montreal, PQ, Canada
[2] Univ Montreal, Dept Social & Prevent Med, Montreal, PQ, Canada
[3] Montreal Chest Inst, Immunodeficiency Serv, Montreal, PQ, Canada
[4] McGill Univ, Ctr Hlth, Royal Victoria Hosp, Div Hematol, Montreal, PQ, Canada
[5] McGill Aids Ctr, Montreal, PQ, Canada
关键词
HIV; genotypic testing; drug resistance; V-shape relationship; antiretroviral drug failure;
D O I
10.1002/jmv.20582
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Previous studies on patients who develop drug resistant HIV-1 variants have shown that continued use of failing regimens might provide clinical benefit. However, the effect of long-term exposure to drug resistant variants may lead to emergence of compensatory mutations that may jeopardize this effect. In this study, we assess associations among type and number of drug resistant mutations, viral load and disease progression in patients with long-term follow up. Patients with genotypic testing performed at the time of treatment failure were enrolled. Comparison of viral load and CD4 cell count between different resistance groups was performed using analysis of variance. Multiple linear regression analysis was performed to assess the simultaneous effects of the presence of particular mutations and their accumulation on viral load. Data from 475 patients who were followed for a median of 43 months from October 1999 to July 2005 were studied. A "V shape" relationship was observed between the number of mutations and viral load. Specifically, in patients harboring upto five mutations, viral load was reduced by 0.8 log/ copies when compared to wild-type variants. However, with more than six mutations viral load progressively increased. Certain reverse transcriptase mutations such as M184V/I, K70R, V1081, and protease mutations such as L33FIV, M84V, and M361 were associated with reduced viral load. Together, these findings suggest that long-term maintenance of a sub-optimal antiretroviral regimen may have deleterious consequences for the patient. (c) 2006 Wiley-Liss, Inc.
引用
收藏
页码:608 / 613
页数:6
相关论文
共 24 条
[1]   Evolution of phenotypic drug susceptibility and viral replication capacity during long-term virologic failure of protease inhibitor therapy in human immunodeficiency virus-infected adults [J].
Barbour, JD ;
Wrin, T ;
Grant, RM ;
Martin, JN ;
Segal, MR ;
Petropoulos, CJ ;
Deeks, SG .
JOURNAL OF VIROLOGY, 2002, 76 (21) :11104-11112
[2]   Overview of the effectiveness of triple combination therapy in antiretroviral-naive HIV-1 infected adults [J].
Bartlett, JA ;
DeMasi, R ;
Quinn, J ;
Moxham, C ;
Rousseau, F .
AIDS, 2001, 15 (11) :1369-1377
[3]   Individual contributions of mutant protease and reverse transcriptase to viral infectivity, replication, and protein maturation of antiretroviral drug-resistant human immunodeficiency virus type 1 [J].
Bleiber, G ;
Munoz, M ;
Ciuffi, A ;
Meylan, P ;
Telenti, A .
JOURNAL OF VIROLOGY, 2001, 75 (07) :3291-3300
[4]   Role of minority populations of human immunodeficiency virus type 1 in the evolution of viral resistance to protease inhibitors [J].
Charpentier, C ;
Dwyer, DE ;
Mammano, F ;
Lecossier, D ;
Clavel, F ;
Hance, AJ .
JOURNAL OF VIROLOGY, 2004, 78 (08) :4234-4247
[5]  
CLAVEL F, 2005, 12 C RETR OPP INF FE
[6]  
Cozzi-Lepri A, 2003, ANTIVIR THER, V8, P127
[7]   Virologic and immunologic consequences of discontinuing combination antiretroviral-drug therapy in HIV-infected patients with detectable viremia. [J].
Deeks, SG ;
Wrin, T ;
Liegler, T ;
Hoh, R ;
Hayden, M ;
Barbour, JD ;
Hellmann, NS ;
Petropoulos, CJ ;
McCune, JM ;
Hellerstein, MK ;
Grant, RM .
NEW ENGLAND JOURNAL OF MEDICINE, 2001, 344 (07) :472-480
[8]   Sustained CD4+ T cell response after virologic failure of protease inhibitor-based regimens in patients with human immunodeficiency virus infection [J].
Deeks, SG ;
Barbour, JD ;
Martin, JN ;
Swanson, MS ;
Grant, RM .
JOURNAL OF INFECTIOUS DISEASES, 2000, 181 (03) :946-953
[9]   HIV RNA and CD4 cell count response to protease inhibitor therapy in an urban AIDS clinic: Response to both initial and salvage therapy [J].
Deeks, SG ;
Hecht, FM ;
Swanson, M ;
Elbeik, T ;
Loftus, R ;
Cohen, PT ;
Grant, RM .
AIDS, 1999, 13 (06) :F35-F43
[10]  
DeGruttola V, 2000, ANTIVIR THER, V5, P41