Transmission of HIV-1 drug resistance

被引:78
作者
Tang, JW [1 ]
Pillay, D [1 ]
机构
[1] UCL Royal Free & Univ Coll Med Sch, Dept Virol, Windeyer Inst Med Sci, London W1T 4JF, England
关键词
HIV; transmission; drug-naive; drug resistance-associated mutations; genotyping; suboptimal therapy response;
D O I
10.1016/j.jcv.2003.12.002
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Background: The use of highly-active anti-retroviral therapy (HAART) for treating HIV infections is increasing. Recent studies have demonstrated that HAART is improving both the length and quality of life in HIV-infected patients. Resistant strains of HIV arise when drug adherence is poor. This can lead to the transmission of drug-resistant strains of HIV to susceptible individuals. This can lead to suboptimal first-line therapy, if the resistance profile of the transmitted virus is unknown. Objectives: To review the mechanisms of how drug resistance arises; the methods used to characterise drug resistance; the problems arising with compliance leading to the development of drug-resistant HIV strains; the evidence for the incidence, prevalence and trends in the transmission of resistant HIV strains in different risk groups; and the evidence of suboptimal response to first-line therapy where transmission of a resistant HIV strain has occurred. On the basis of this, a case is presented for the routine resistance testing of all newly diagnosed HIV-infected individuals. Study design: Literature review. Results and conclusions: There is evidence, though limited at present, that transmission of drug-resistant HIV strains can lead to suboptimal response to first-line therapy in newly diagnosed HIV-infected individuals. As the use of HAART can only increase in the future, and compliance will always be a problem in such HAART-treated patients, baseline resistance testing should become a routine part of their management. (C) 2003 Elsevier B.V. All rights reserved.
引用
收藏
页码:1 / 10
页数:10
相关论文
共 134 条
[71]   Reduced antiretroviral drug susceptibility among patients with primary HIV infection [J].
Little, SJ ;
Daar, ES ;
D'Aquila, RT ;
Keiser, PH ;
Connick, E ;
Whitcomb, JM ;
Hellmann, NS ;
Petropoulos, CJ ;
Sutton, L ;
Pitt, JA ;
Rosenberg, ES ;
Koup, RA ;
Walker, BD ;
Richman, DD .
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 1999, 282 (12) :1142-1149
[72]   Nucleoside reverse transcriptase inhibitor resistance [J].
Loveday, C .
JOURNAL OF ACQUIRED IMMUNE DEFICIENCY SYNDROMES, 2001, 26 :S10-S24
[73]   Epidemiology of HIV-1 and emerging problems [J].
Lukashov, VV ;
de Ronde, A ;
de Jong, JJ ;
Goudsmit, J .
INTERNATIONAL JOURNAL OF ANTIMICROBIAL AGENTS, 2000, 16 (04) :463-466
[74]   Mutations associated with genotypic resistance to antiretroviral therapy in treatment naive HIV-1 infected patients in Greece [J].
Magiorkinis, E ;
Paraskevis, D ;
Magiorkinis, G ;
Chryssou, S ;
Chini, M ;
Lazanas, M ;
Paparizos, V ;
Saroglou, G ;
Antoniadou, A ;
Giamarellou, E ;
Karafoulidou, A ;
Hatzakis, A .
VIRUS RESEARCH, 2002, 85 (01) :109-115
[75]   Retracing the evolutionary pathways of human immunodeficiency virus type 1 resistance to protease inhibitors: Virus fitness in the absence and in the presence of drug [J].
Mammano, F ;
Trouplin, V ;
Zennou, V ;
Clavel, F .
JOURNAL OF VIROLOGY, 2000, 74 (18) :8524-8531
[76]   LOWER IN-VIVO MUTATION-RATE OF HUMAN-IMMUNODEFICIENCY-VIRUS TYPE-1 THAN THAT PREDICTED FROM THE FIDELITY OF PURIFIED REVERSE-TRANSCRIPTASE [J].
MANSKY, LM ;
TEMIN, HM .
JOURNAL OF VIROLOGY, 1995, 69 (08) :5087-5094
[77]   Replicative fitness of protease inhibitor-resistant mutants of human immunodeficiency virus type 1 [J].
Martinez-Picado, J ;
Savara, LV ;
Sutton, L ;
D'Aquila, RT .
JOURNAL OF VIROLOGY, 1999, 73 (05) :3744-3752
[78]  
Masquelier B, 2001, J ACQ IMMUN DEF SYND, V27, P99, DOI 10.1097/00126334-200106010-00001
[79]   Blocking the docking of HIV-1 [J].
McKnight, D ;
Weiss, RA .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2003, 100 (19) :10581-10582
[80]   Resistance to protease inhibitors [J].
Miller, V .
JOURNAL OF ACQUIRED IMMUNE DEFICIENCY SYNDROMES, 2001, 26 :S34-S50