TMC310911, a Novel Human Immunodeficiency Virus Type 1 Protease Inhibitor, Shows In Vitro an Improved Resistance Profile and Higher Genetic Barrier to Resistance Compared with Current Protease Inhibitors
Authors
Dierynck, IngeVan Marck, Herwig
Van Ginderen, Marcia
Jonckers, Tim H. M.
Nalam, Madhavi N. L.
Schiffer, Celia A.
Raoof, Araz
Kraus, Guenter
Picchio, Gaston
UMass Chan Affiliations
Department of Biochemistry and Molecular PharmacologyDocument Type
Journal ArticlePublication Date
2011-12-08Keywords
Drug Resistance, ViralHIV Antigens
HIV Protease Inhibitors
HIV-1
Humans
Virus Replication
gag Gene Products, Human Immunodeficiency Virus
Biochemistry, Biophysics, and Structural Biology
Microbiology
Metadata
Show full item recordAbstract
TMC310911 is a novel human immunodeficiency virus type 1 (HIV-1) protease inhibitor (PI) structurally closely related to darunavir (DRV) but with improved virological characteristics. TMC310911 has potent activity against wild-type (WT) HIV-1 (median 50% effective concentration [EC(50)], 14 nM) and a wide spectrum of recombinant HIV-1 clinical isolates, including multiple-PI-resistant strains with decreased susceptibility to currently approved PIs (fold change [FC] in EC(50), >10). For a panel of 2,011 recombinant clinical isolates with decreased susceptibility to at least one of the currently approved PIs, the FC in TMC310911 EC(50) wasSource
Antimicrob Agents Chemother. 2011 Dec;55(12):5723-31. Epub 2011 Sep 6. Link to article on publisher's siteDOI
10.1128/AAC.00748-11Permanent Link to this Item
http://hdl.handle.net/20.500.14038/26001PubMed ID
21896904Related Resources
Link to Article in PubMedae974a485f413a2113503eed53cd6c53
10.1128/AAC.00748-11