HIV resistance to antiretroviral drugs: Mechanisms, genotypic and phenotypic resistance testing in clinical practice

被引:18
作者
Blaise, P
Clevenbergh, R
Vaira, D
Moutschen, M
Dellamonica, P
机构
[1] CHU Liege, Liege, Belgium
[2] CHU Nice, Serv Maladies Infect & Trop, Nice, France
[3] CHU Liege, Lab Reference SIDA, Liege, Belgium
[4] CHU Liege, Serv Malad Infect, Liege, Belgium
关键词
HIV drug resistance; genotypic resistance testing; phenotypic resistance testing; antiretrovirals;
D O I
10.1179/acb.2002.041
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
HIV resistance to antiretroviral agents is a major contributory cause of treatment failure. The dynamics of HIV replication, together with patient-, physician-, and drug-related factors, lead to emergence of HIV resistant strains in most of the patients. Phenotypic assays look for an increase in the antiretroviral drug (ARV) concentration that inhibits 50% of the growth of the tested HIV strain (IC50), comparatively with a reference strain cultivated in parallel. Genotypic tests detect resistance mutations in the reverse transcriptase and protease genes by comparing the gene sequences of a resistant virus to those of a wildtype strain that has previously been described. The efficacy of each ARV class and each individual ARV is threatened by specific mutations and resistance mechanisms. In retrospective studies of genotypic or phenotypic resistance testing, baseline resistance tests results were correlated with virological outcomes. There is some evidence from prospective studies that resistance testing may have some benefits when used to choose salvage regimens. However, problems in the areas of test interpretation, patient compliance, availability of active drugs, and technical test performance limit the usefulness of resistance testing in clinical practice. This article reviews the mechanisms underlying HIV resistance, the principles of phenotypic and genotypic tests, and the use of these tests in clinical practice.
引用
收藏
页码:191 / 201
页数:11
相关论文
共 54 条
[11]   IN-VIVO EMERGENCE OF HIV-1 VARIANTS RESISTANT TO MULTIPLE PROTEASE INHIBITORS [J].
CONDRA, JH ;
SCHLEIF, WA ;
BLAHY, OM ;
GABRYELSKI, LJ ;
GRAHAM, DJ ;
QUINTERO, JC ;
RHODES, A ;
ROBBINS, HL ;
ROTH, E ;
SHIVAPRAKASH, M ;
TITUS, D ;
YANG, T ;
TEPPLER, H ;
SQUIRES, KE ;
DEUTSCH, PJ ;
EMINI, EA .
NATURE, 1995, 374 (6522) :569-571
[12]  
COSTAGLIOLA D, 2001, 8 C RETR OPP INF FEB
[13]   Insertion of two amino acids combined with changes in reverse transcriptase containing tyrosine-215 of HIV-1 resistant to multiple nucleoside analogs [J].
de Jong, JJ ;
Goudsmit, J ;
Lukashov, VV ;
Hillebrand, ME ;
Baan, E ;
Huismans, R ;
Danner, SA ;
ten Veen, JH ;
de Wolf, F ;
Jurriaans, S .
AIDS, 1999, 13 (01) :75-80
[14]   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
[15]  
DeGruttola V, 2000, ANTIVIR THER, V5, P41
[16]  
DELUCA A, 2001, 8 C RETR OPP INF FEB
[17]  
DEMETER L, 2000, 7 C RETR OPP INF JAN
[18]   Factors influencing the emergence of resistance to indinavir: Role of virologic, immunologic, and pharmacologic variables [J].
Drusano, GL ;
Bilello, JA ;
Stein, DS ;
Nessly, M ;
Meibohm, A ;
Emini, EA ;
Deutsch, P ;
Condra, J ;
Chodakewitz, J ;
Holder, DJ .
JOURNAL OF INFECTIOUS DISEASES, 1998, 178 (02) :360-367
[19]   Importance of protease inhibitor plasma levels in HIV-infected patients treated with genotypic-guided therapy: pharmacological data from the Viradapt Study [J].
Durant, J ;
Clevenbergh, P ;
Garraffo, R ;
Halfon, P ;
Icard, S ;
Del Giudice, P ;
Montagne, N ;
Schapiro, JM ;
Dellamonica, P .
AIDS, 2000, 14 (10) :1333-1339
[20]   Drug-resistance genotyping in HIV-1 therapy: the VIRADAPT randomised controlled trial [J].
Durant, J ;
Clevenbergh, P ;
Halfon, P ;
Delgiudice, P ;
Porsin, S ;
Simonet, P ;
Montagne, N ;
Boucher, CAB ;
Schapiro, JM ;
Dellamonica, P .
LANCET, 1999, 353 (9171) :2195-2199