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
[11]   HIV POPULATION-DYNAMICS IN-VIVO - IMPLICATIONS FOR GENETIC-VARIATION, PATHOGENESIS, AND THERAPY [J].
COFFIN, JM .
SCIENCE, 1995, 267 (5197) :483-489
[12]  
COHEN C, 2006, 15 INT AIDS C 13 18
[13]  
COOPER D, 2007, 14 C RETR OPP INF FE
[14]  
COOPER D, 2005, 12 C RETR OPP INF 22
[15]   Relationship between drug resistance mutations, plasma viremia, and CD4+ T-cell counts in patients with chronic HIV infection [J].
de Mendoza, C ;
Martín-Carbonero, L ;
Gallego, O ;
Corral, A ;
González-Lahoz, J ;
Soriano, V .
JOURNAL OF MEDICAL VIROLOGY, 2005, 76 (01) :1-6
[16]  
DEBETHUNE MP, 2005, 12 C RETR OPP INF 22
[17]   Duration and predictors of CD4 T-cell gains in patients who continue combination therapy despite detectable plasma viremia [J].
Deeks, SG ;
Barbour, JD ;
Grant, RM ;
Martin, JN .
AIDS, 2002, 16 (02) :201-207
[18]   Treatment of anti retroviral-drug-resistant HIV-1 infection [J].
Deeks, SG .
LANCET, 2003, 362 (9400) :2002-2011
[19]   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
[20]   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