Resistance profiles in patients with viral rebound on potent antiretroviral therapy

被引:34
作者
Lepri, AC
Sabin, CA
Staszewski, S
Hertogs, K
Müller, A
Rabenau, H
Philips, AN
Miller, V
机构
[1] Univ Frankfurt Klinikum, Zentrum Inneren Med, D-60590 Frankfurt, Germany
[2] UCL Royal Free & Univ Coll, Sch Med, Royal Free Ctr HIV Med, London, England
[3] UCL Royal Free & Univ Coll, Sch Med, Dept Primary Care & Populat Sci, London, England
[4] Goethe Univ Frankfurt, Zentrum Inneren Med, D-6000 Frankfurt, Germany
[5] Goethe Univ Frankfurt, Inst Med Virol, D-6000 Frankfurt, Germany
[6] VIRCO, Mechelen, Belgium
关键词
D O I
10.1086/315301
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 prevalence of phenotypic drug resistance was assessed in 60 patients with a viral rebound after they received a protease inhibitor (PI)- or nonnucleoside reverse transcriptase inhibitor (NNRTI)-containing regimen (baseline), Resistance testing was done within 36 weeks of viral rebound; no resistance testing was available at baseline, All patients had previously received zidovudine; 86.0% had received lamivudine, In total, 45.1% of the patients had strains resistant to the PI that they started and 88.9% given nevirapine had strains with reduced susceptibility to that drug. Overall, 46 patients (76.7%) harbored a strain resistant to greater than or equal to 1 drug of their initial PI- or NNRTI-containing regimen. Of 53 patients who remained on treatment at the time of the study (40 had switched to a different combination from that at baseline), 6 harbored isolates susceptible to all drugs they had ever received. Thus, patients with viral rebound while on potent antiretroviral therapy usually have reduced susceptibility to greater than or equal to 1 drug. Viral rebound also occurs in persons in whom resistant strains could not be detected by the assay used.
引用
收藏
页码:1143 / 1147
页数:5
相关论文
共 15 条
[1]   Activity of a ritonavir plus saquinavir-containing regimen in patients with virologic evidence of indinavir or ritonavir failure [J].
Deeks, SG ;
Grant, RM ;
Beatty, GW ;
Horton, C ;
Detmer, J ;
Eastman, S .
AIDS, 1998, 12 (10) :F97-F102
[2]  
DEEKS SG, 1998, 2 INT WORKSH DRUG RE
[3]  
DEPASQUALE MP, 1998, 2 INT WORKSH DRUG RE
[4]   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
[5]  
HAVLIR DV, 1998, 2 INT WORKSH DRUG RE
[6]  
HELLMANN N, 1999, ANTIVIR THER S, V4, P34
[7]   Activities of cefepime and five other antibiotics against nosocomial PER-1-type and/or OXA-10-type β-lactamase-producing Pseudomonas aeruginosa and Acinetobacter spp. -: J Antimicrob Chemother 1998; 42:269-270 [J].
Vahaboglu, H ;
Saribas, S ;
Akbal, H ;
Ozturk, R ;
Yucel, A .
JOURNAL OF ANTIMICROBIAL CHEMOTHERAPY, 1998, 42 (02) :269-270
[8]  
JOHNSON VA, 1997, ANTIVIR THER S, V2, P72
[9]  
KATZENSTEIN DA, 1998, 2 INT WORKSH DRUG RE
[10]  
MAYERS DL, 1997, ANTIVIR THER S, V2, P72