Literature DB >> 12457443

Enfuvirtide.

Ray Y Chen1, J Michael Kilby, Michael S Saag.   

Abstract

Despite the overall success of antiretroviral medications in reducing the morbidity and mortality associated with HIV infection, many patients on treatment suffer progressive disease due to intolerance or the development of resistant viral strains. Consequently, considerable research focuses on the development of new classes of antiretroviral agents with mechanisms of action different to the current classes. Enfuvirtide (T-20, pentafuside, Fuzeon), the first drug of a new class of antiretroviral medications known as fusion inhibitors, blocks the fusion of the virus particle with the host target cell. The viral entry process begins with the attachment of viral surface glycoprotein gp120 to the host cell CD4 and chemokine receptor sites. Viral gp41 then undergoes a conformational change enabling fusion of both membranes, a critical step in the viral life cycle. Enfuvirtide is a synthetic peptide that binds to gp41, preventing the conformational change required for membrane fusion. Based on potent in vitro activity, a Phase I clinical trial of intravenous enfuvirtide was conducted that demonstrated a substantial decline in HIV plasma viral load in the highest dose group and no serious adverse effects. Phase II trials evaluated regimens of both continuous subcutaneous infusions and intermittent subcutaneous injections. Intermittent injections were pharmacokinetically superior to continuous infusions and were associated with fewer administration difficulties. For some subjects who added enfuvirtide monotherapy to an already failing regimen, the beneficial effect on viral load reduction appeared short-lived, suggesting the development of resistance. Two large randomised clinical trials comparing "optimised background" (best available, individualised regimens based on patient history and resistance assays) versus optimised background plus enfuvirtide have recently shown a significant virological advantage (approximately 1 log(10) difference from controls) at 24 weeks. In all trials to date, very few significant adverse effects have been seen--minor injection site reactions are frequent, but rarely treatment limiting. Based on these studies, enfuvirtide will likely play a significant role in the treatment of patients with limited treatment options.

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Year:  2002        PMID: 12457443     DOI: 10.1517/13543784.11.12.1837

Source DB:  PubMed          Journal:  Expert Opin Investig Drugs        ISSN: 1354-3784            Impact factor:   6.206


  10 in total

Review 1.  Enfuvirtide.

Authors:  Toni M Dando; Caroline M Perry
Journal:  Drugs       Date:  2003       Impact factor: 9.546

2.  Evaluation of "credit card" libraries for inhibition of HIV-1 gp41 fusogenic core formation.

Authors:  Yang Xu; Hong Lu; Jack P Kennedy; Xuxia Yan; Laura A McAllister; Noboru Yamamoto; Jason A Moss; Grant E Boldt; Shibo Jiang; Kim D Janda
Journal:  J Comb Chem       Date:  2006 Jul-Aug

3.  Maraviroc (UK-427,857), a potent, orally bioavailable, and selective small-molecule inhibitor of chemokine receptor CCR5 with broad-spectrum anti-human immunodeficiency virus type 1 activity.

Authors:  Patrick Dorr; Mike Westby; Susan Dobbs; Paul Griffin; Becky Irvine; Malcolm Macartney; Julie Mori; Graham Rickett; Caroline Smith-Burchnell; Carolyn Napier; Rob Webster; Duncan Armour; David Price; Blanda Stammen; Anthony Wood; Manos Perros
Journal:  Antimicrob Agents Chemother       Date:  2005-11       Impact factor: 5.191

Review 4.  Pharmacokinetics, pharmacodynamics and drug interaction potential of enfuvirtide.

Authors:  Indravadan H Patel; Xiaoping Zhang; Keith Nieforth; Miklos Salgo; Neil Buss
Journal:  Clin Pharmacokinet       Date:  2005       Impact factor: 6.447

5.  Identification of novel cellular targets for therapeutic intervention against Ebola virus infection by siRNA screening.

Authors:  Andrey A Kolokoltsov; Mohammad F Saeed; Alexander N Freiberg; Michael R Holbrook; Robert A Davey
Journal:  Drug Dev Res       Date:  2009-06-01       Impact factor: 4.360

6.  Structural basis for highly effective HIV-1 neutralization by CD4-mimetic miniproteins revealed by 1.5 Å cocrystal structure of gp120 and M48U1.

Authors:  Priyamvada Acharya; Timothy S Luongo; Mark K Louder; Krisha McKee; Yongping Yang; Young Do Kwon; John R Mascola; Pascal Kessler; Loïc Martin; Peter D Kwong
Journal:  Structure       Date:  2013-05-23       Impact factor: 5.006

7.  Selection of predicted siRNA as potential antiviral therapeutic agent against influenza virus.

Authors:  Asif Raza; Hira Shareef; Hira Salim; Rashid Khushal; Habib Bokhari
Journal:  Bioinformation       Date:  2011-07-19

Review 8.  Opening the door on entry inhibitors in HIV: Redefining the use of entry inhibitors in heavily treatment experienced and treatment-limited individuals living with HIV.

Authors:  Chloe Orkin; Pedro Cahn; Antonella Castagna; Brinda Emu; P Richard Harrigan; Daniel R Kuritzkes; Mark Nelson; Jonathan Schapiro
Journal:  HIV Med       Date:  2022-03-16       Impact factor: 3.094

9.  Enfuvirtide antiretroviral therapy in HIV-1 infection.

Authors:  Christina Mr Kitchen; Miriam Nuño; Scott G Kitchen; Paul Krogstad
Journal:  Ther Clin Risk Manag       Date:  2008-04       Impact factor: 2.423

Review 10.  Broad-Spectrum Coronavirus Fusion Inhibitors to Combat COVID-19 and Other Emerging Coronavirus Diseases.

Authors:  Xinling Wang; Shuai Xia; Qian Wang; Wei Xu; Weihua Li; Lu Lu; Shibo Jiang
Journal:  Int J Mol Sci       Date:  2020-05-28       Impact factor: 5.923

  10 in total

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