Literature DB >> 19192935

Novel targets for antiretroviral therapy: clinical progress to date.

Birgitt Dau1, Mark Holodniy.   

Abstract

The advent of HIV-1 resistance to antiretroviral medications, the need for lifelong antiretroviral therapy (ART) for HIV-infected individuals, and the goal of minimizing ART-related adverse effects and toxicity all drive the need for new antiretroviral drugs. Two new classes of antiretroviral medications for HIV treatment, the CCR5 and integrase inhibitors, have recently been approved for use in patients in whom previous HIV treatment regimens have failed. These new agent classes are a welcome addition to other antiretroviral classes, which include nucleoside reverse transcriptase inhibitors, non-nucleoside reverse transcriptase inhibitors, protease inhibitors and fusion inhibitors. Maraviroc is a CCR5 co-receptor antagonist that blocks HIV binding to the CCR5 receptor, which is a CD4 co-receptor necessary for cell entry. It is approved for use in ART-experienced patients with CCR5-tropic HIV, and was found to significantly reduce HIV viral load and increase CD4+ cell count when combined with an optimized background ART regimen (OBR). Treatment failure with maraviroc has been described and is primarily associated with the presence of CXCR4-tropic virus. Vicriviroc is another CCR5 co-receptor antagonist that is in late clinical trials. Raltegravir is the first US FDA-approved HIV-1 integrase inhibitor. It is approved for use in ART-experienced patients and was found to significantly reduce HIV viral load and increase CD4+ cell counts compared with placebo in combination with an OBR. Raltegravir has also been studied in treatment-naive patients and was found to be non-inferior to an efavirenz-based regimen. Elvitegravir is another HIV-1 integrase inhibitor in clinical development. Other new antiretroviral agents in clinical development include PRO140, a monoclonal antibody against CCR5, and bevirimat, a maturation inhibitor that prevents late-stage gag polyprotein processing. A number of other drug targets, such as CCR5 co-receptor agonists, CXCR4 co-receptor antagonists, novel fusion inhibitors, and alternative antiretroviral strategies, such as immune stimulation and gene therapy, are under investigation.

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Year:  2009        PMID: 19192935     DOI: 10.2165/00003495-200969010-00003

Source DB:  PubMed          Journal:  Drugs        ISSN: 0012-6667            Impact factor:   9.546


  71 in total

1.  Epidemiology and predictive factors for chemokine receptor use in HIV-1 infection.

Authors:  Graeme J Moyle; Adrian Wildfire; Sundhiya Mandalia; Howard Mayer; James Goodrich; Jeannette Whitcomb; Brian G Gazzard
Journal:  J Infect Dis       Date:  2005-02-11       Impact factor: 5.226

2.  The Anti-HIV potency of cyclotriazadisulfonamide analogs is directly correlated with their ability to down-modulate the CD4 receptor.

Authors:  Kurt Vermeire; Thomas W Bell; Heung-Jin Choi; Qi Jin; Meinrado F Samala; Andrej Sodoma; Erik De Clercq; Dominique Schols
Journal:  Mol Pharmacol       Date:  2003-01       Impact factor: 4.436

3.  Naphthalene sulfonate polymers with CD4-blocking and anti-human immunodeficiency virus type 1 activities.

Authors:  S Rusconi; M Moonis; D P Merrill; P V Pallai; E A Neidhardt; S K Singh; K J Willis; M S Osburne; A T Profy; J C Jenson; M S Hirsch
Journal:  Antimicrob Agents Chemother       Date:  1996-01       Impact factor: 5.191

4.  Gene transfer in humans using a conditionally replicating lentiviral vector.

Authors:  Bruce L Levine; Laurent M Humeau; Jean Boyer; Rob-Roy MacGregor; Tessio Rebello; Xiaobin Lu; Gwendolyn K Binder; Vladimir Slepushkin; Franck Lemiale; John R Mascola; Frederic D Bushman; Boro Dropulic; Carl H June
Journal:  Proc Natl Acad Sci U S A       Date:  2006-11-07       Impact factor: 11.205

5.  Safety, pharmacokinetics, and antiviral activity of AMD3100, a selective CXCR4 receptor inhibitor, in HIV-1 infection.

Authors:  Craig W Hendrix; Ann C Collier; Michael M Lederman; Dominique Schols; Richard B Pollard; Stephen Brown; J Brooks Jackson; Robert W Coombs; Marshall J Glesby; Charles W Flexner; Gary J Bridger; Karin Badel; Ronald T MacFarland; Geoffrey W Henson; Gary Calandra
Journal:  J Acquir Immune Defic Syndr       Date:  2004-10-01       Impact factor: 3.731

6.  Long-term clinical and surrogate marker effects of subcutaneous intermittent interleukin-2 without antiretroviral therapy in HIV-infected patients.

Authors:  C Herzmann; Z Cuthbertson; L Fosdick; M Fisher; M Nelson; N Perry; M Law; H Wand; G Janossy; M A Johnson; M Youle
Journal:  J Antimicrob Chemother       Date:  2008-06-27       Impact factor: 5.790

7.  Safety and tolerability of vaginal PRO 2000 gel in sexually active HIV-uninfected and abstinent HIV-infected women.

Authors:  Kenneth H Mayer; Salim Abdool Karim; Clifton Kelly; Lisa Maslankowski; Helen Rees; Albert T Profy; Jennifer Day; Julie Welch; Zeda Rosenberg
Journal:  AIDS       Date:  2003-02-14       Impact factor: 4.177

8.  CADA, a potential anti-HIV microbicide that specifically targets the cellular CD4 receptor.

Authors:  Kurt Vermeire; Joachim Brouwers; Yven Van Herrewege; Roger Le Grand; Guido Vanham; Patrick Augustijns; Thomas W Bell; Dominique Schols
Journal:  Curr HIV Res       Date:  2008-05       Impact factor: 1.581

9.  Maraviroc for previously treated patients with R5 HIV-1 infection.

Authors:  Roy M Gulick; Jacob Lalezari; James Goodrich; Nathan Clumeck; Edwin DeJesus; Andrzej Horban; Jeffrey Nadler; Bonaventura Clotet; Anders Karlsson; Michael Wohlfeiler; John B Montana; Mary McHale; John Sullivan; Caroline Ridgway; Steve Felstead; Michael W Dunne; Elna van der Ryst; Howard Mayer
Journal:  N Engl J Med       Date:  2008-10-02       Impact factor: 91.245

10.  Neurokinin-1 receptor antagonist (aprepitant) inhibits drug-resistant HIV-1 infection of macrophages in vitro.

Authors:  Xu Wang; Steven D Douglas; Jian-Ping Lai; Florin Tuluc; Pablo Tebas; Wen-Zhe Ho
Journal:  J Neuroimmune Pharmacol       Date:  2007-01-12       Impact factor: 4.147

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  26 in total

1.  In vitro antiviral characteristics of HIV-1 attachment inhibitor BMS-626529, the active component of the prodrug BMS-663068.

Authors:  Beata Nowicka-Sans; Yi-Fei Gong; Brian McAuliffe; Ira Dicker; Hsu-Tso Ho; Nannan Zhou; Betsy Eggers; Pin-Fang Lin; Neelanjana Ray; Megan Wind-Rotolo; Li Zhu; Antara Majumdar; David Stock; Max Lataillade; George J Hanna; John D Matiskella; Yasutsugu Ueda; Tao Wang; John F Kadow; Nicholas A Meanwell; Mark Krystal
Journal:  Antimicrob Agents Chemother       Date:  2012-04-30       Impact factor: 5.191

2.  Antiviral activity, pharmacokinetics, and safety of BMS-488043, a novel oral small-molecule HIV-1 attachment inhibitor, in HIV-1-infected subjects.

Authors:  George J Hanna; Jacob Lalezari; James A Hellinger; David A Wohl; Richard Nettles; Anna Persson; Mark Krystal; Pinfang Lin; Richard Colonno; Dennis M Grasela
Journal:  Antimicrob Agents Chemother       Date:  2010-11-15       Impact factor: 5.191

3.  Anti-HIV-1 therapeutics: from FDA-approved drugs to hypothetical future targets.

Authors:  Catherine S Adamson; Eric O Freed
Journal:  Mol Interv       Date:  2009-04

4.  Activity of the HIV-1 attachment inhibitor BMS-626529, the active component of the prodrug BMS-663068, against CD4-independent viruses and HIV-1 envelopes resistant to other entry inhibitors.

Authors:  Zhufang Li; Nannan Zhou; Yongnian Sun; Neelanjana Ray; Max Lataillade; George J Hanna; Mark Krystal
Journal:  Antimicrob Agents Chemother       Date:  2013-06-17       Impact factor: 5.191

5.  Aloperine and Its Derivatives as a New Class of HIV-1 Entry Inhibitors.

Authors:  Zhao Dang; Lei Zhu; Weihong Lai; Hal Bogerd; Kuo-Hsiung Lee; Li Huang; Chin-Ho Chen
Journal:  ACS Med Chem Lett       Date:  2016-01-09       Impact factor: 4.345

6.  Identification, structural modification, and dichotomous effects on human immunodeficiency virus type 1 (HIV-1) replication of ingenane esters from Euphorbia kansui.

Authors:  Qingbo Liu; Wei Li; Li Huang; Yoshihisa Asada; Susan L Morris-Natschke; Chin-Ho Chen; Kuo-Hsiung Lee; Kazuo Koike
Journal:  Eur J Med Chem       Date:  2018-07-19       Impact factor: 6.514

7.  Accurate and efficient gp120 V3 loop structure based models for the determination of HIV-1 co-receptor usage.

Authors:  Majid Masso; Iosif I Vaisman
Journal:  BMC Bioinformatics       Date:  2010-10-05       Impact factor: 3.169

8.  YM201636, an inhibitor of retroviral budding and PIKfyve-catalyzed PtdIns(3,5)P2 synthesis, halts glucose entry by insulin in adipocytes.

Authors:  Ognian C Ikonomov; Diego Sbrissa; Assia Shisheva
Journal:  Biochem Biophys Res Commun       Date:  2009-03-14       Impact factor: 3.575

9.  Novel inhibitors of severe acute respiratory syndrome coronavirus entry that act by three distinct mechanisms.

Authors:  Adeyemi O Adedeji; William Severson; Colleen Jonsson; Kamalendra Singh; Susan R Weiss; Stefan G Sarafianos
Journal:  J Virol       Date:  2013-05-15       Impact factor: 5.103

10.  Comparative analysis of cell culture and prediction algorithms for phenotyping of genetically diverse HIV-1 strains from Cameroon.

Authors:  Viswanath Ragupathy; Jiangqin Zhao; Xue Wang; Owen Wood; Sherwin Lee; Sherri Burda; Phillipe Nyambi; Indira Hewlett
Journal:  AIDS Res Ther       Date:  2009-11-25       Impact factor: 2.250

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