Overcoming resistance to existing therapies in HIV-infected patients: The role of new antiretroviral drugs

被引:38
作者
Perno, Carlo-Federico [1 ]
Moyle, Graeme [2 ]
Tsoukas, Chris [3 ]
Ratanasuwan, Winai [4 ]
Gatell, Jose [5 ]
Schechter, Mauro [6 ]
机构
[1] Univ Roma Tor Vergata, Dept Expt Med & Biochem Sci, I-00133 Rome, Italy
[2] Chelsea & Westminster Hosp, London, England
[3] Montreal Gen Hosp, Div Clin Immunol, Immune Deficiency Treatment Ctr, Montreal, PQ H3G 1A4, Canada
[4] Mahidol Univ, Siriraj Hosp, Dept Prevent & Social Med, Fac Med, Bangkok 10700, Thailand
[5] Univ Barcelona, Infect Dis & AIDS Unit, Barcelona, Spain
[6] Univ Fed Rio de Janeiro, Hosp Univ Clementino Fraga Filho, Rio De Janeiro, Brazil
关键词
treatment-experienced; triple class failure; entry inhibitor; integrase inhibitor;
D O I
10.1002/jmv.21034
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Resistance to available antiretroviral (ARV) agents is of increasing concern, and development of novel agents that address this problem has been identified as a major public health priority. As ARV resistance becomes more prevalent with extended use of existing agents, individuals with HIV infection resistant to all three traditional classes of ARVs, nucleoside reverse transcriptase inhibitors (NRTIs), non-nucleoside reverse transcriptase inhibitors (NNRTls) and protease inhibitors (PIs), find themselves increasingly limited with regard to effective treatment options. The need for tolerable new drug regimens that effectively suppress viral replication while being simple to adhere to is increasingly pressing. This article reviews the epidemiology of antiretroviral drug resistance, the factors that contribute to the emergence of resistance, and presents data that support the need for early detection of resistance and maximal virologic suppression in order to delay treatment failure and reduce mortality. Healthcare providers are encouraged to optimize therapy through the use of new agents from existing drug classes, which can minimize cross-resistance, as well as agents with novel mechanisms of action, in order to realize the potential for greater viral containment and to forestall development of resistance mutations. This article evaluates several emerging therapies that are in late-stage clinical development and promise to expand treatment options for highly treatment-experienced patients with the goal of improving outcomes for HIV-infected individuals whose options for sustained antiviral efficacy are increasingly limited.
引用
收藏
页码:565 / 576
页数:12
相关论文
共 85 条
[1]   TMC125, a novel next-generation nonnucleoside reverse transcriptase inhibitor active against nonnucleoside reverse transcriptase inhibitor-resistant human immunodeficiency virus type 1 [J].
Andries, K ;
Azijn, H ;
Thielemans, T ;
Ludovici, D ;
Kukla, M ;
Heeres, J ;
Janssen, P ;
De Corte, B ;
Vingerhoets, J ;
Pauwels, R ;
de Béthune, MP .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 2004, 48 (12) :4680-4686
[2]   Specific mutations in HIV-1 gp41 are associated with immunological success in HIV-1-infected patients receiving enfuvirtide treatment [J].
Aquaro, Stefano ;
D'Arrigo, Roberta ;
Svicher, Valentina ;
Di Perri, Giovanni ;
Caputo, Sergio Lo ;
Visco-Comandini, Ubaldo ;
Santoro, Mario ;
Bertoli, Ada ;
Mazzotta, Francesco ;
Bonora, Stefano ;
Tozzi, Valerio ;
Bellagamba, Rita ;
Zaccarelli, Mauro ;
Narciso, Pasquale ;
Antinori, Andrea ;
Perno, Carlo Federico .
JOURNAL OF ANTIMICROBIAL CHEMOTHERAPY, 2006, 58 (04) :714-722
[3]  
Back D, 2006, 8 INT C DRUG THER HI
[4]   How does expert advice impact genotypic resistance testing in clinical practice? [J].
Badri, SM ;
Adeyemi, OM ;
Max, BE ;
Zagorski, BM ;
Barker, DE .
CLINICAL INFECTIOUS DISEASES, 2003, 37 (05) :708-713
[5]   Less than 95% adherence to nonnucleoside reverse-transcriptase inhibitor therapy can lead to viral suppression [J].
Bangsberg, David R. .
CLINICAL INFECTIOUS DISEASES, 2006, 43 (07) :939-941
[6]   Adherence-resistance relationships for protease and non-nucleoside reverse transcriptase inhibitors explained by virological fitness [J].
Bangsberg, DR ;
Acosta, EP ;
Gupta, R ;
Guzman, D ;
Riley, ED ;
Harrigan, PR ;
Parkin, N ;
Deeks, SG .
AIDS, 2006, 20 (02) :223-231
[7]  
BATTEGAY M, 2003, 2 IAS C HIV PATH TRE
[8]  
BENNETT D, 2005, 12 C RETR OPP INF 22
[9]  
BOFFITO M, 2006, 13 C RETR OPP INF 5
[10]   Prevalence and predictors of antiretroviral drug resistance in newly diagnosed HIV-1 infection [J].
Booth, Clare L. ;
Garcia-Diaz, Ana M. ;
Youle, Michael S. ;
Johnson, Margaret A. ;
Phillips, Andrew ;
Geretti, Anna Maria .
JOURNAL OF ANTIMICROBIAL CHEMOTHERAPY, 2007, 59 (03) :517-524