Antiviral activity of tenofovir (PMPA) against nucleoside-resistant clinical HIV samples

被引:70
作者
Miller, MD
Margot, NA
Hertogs, K
Larder, B
Miller, V
机构
[1] Gilead Sci Inc, Foster City, CA 94404 USA
[2] Virco, Mechelen, Belgium
[3] Virco, Cambridge, England
[4] Univ Frankfurt, D-6000 Frankfurt, Germany
关键词
D O I
10.1081/NCN-100002483
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The presence of the lamivudine-associated M184V RT mutation increases tenofovir susceptibility in multiple HIV genotypes. Tenofovir is uniquely active against multinucleoside-resistant HIV expressing the Q151M mutation, but shows reduced susceptibility to the T69S insertion mutations. HIV with common forms of zidovudine and lamivudine resistance are susceptible to tenofovir, corroborating phase II clinical results demonstrating the activity of tenofovir DF in treatment-experienced patients.
引用
收藏
页码:1025 / 1028
页数:4
相关论文
共 10 条
[1]   DIFFERENTIAL ANTIHERPESVIRUS AND ANTIRETROVIRUS EFFECTS OF THE (S) AND (R) ENANTIOMERS OF ACYCLIC NUCLEOSIDE PHOSPHONATES - POTENT AND SELECTIVE INVITRO AND INVIVO ANTIRETROVIRUS ACTIVITIES OF (R)-9-(2-PHOSPHONOMETHOXYPROPYL)-2,6-DIAMINOPURINE [J].
BALZARINI, J ;
HOLY, A ;
JINDRICH, J ;
NAESENS, L ;
SNOECK, R ;
SCHOLS, D ;
DECLERCQ, E .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 1993, 37 (02) :332-338
[2]  
BLOOR S, 2000, 4 INT WORKSH HIV DRU
[3]   Mutations in the pol gene of human immunodeficiency virus type 1 in infected patients receiving didanosine and hydroxyurea combination therapy [J].
DeAntoni, A ;
Foli, A ;
Lisziewicz, J ;
Lori, F .
JOURNAL OF INFECTIOUS DISEASES, 1997, 176 (04) :899-903
[4]  
DEEKS S, 1998, 5 C RETR OPP INF CHI
[5]   IDENTIFICATION OF A MUTATION AT CODON-65 IN THE IKKK MOTIF OF REVERSE-TRANSCRIPTASE THAT ENCODES HUMAN-IMMUNODEFICIENCY-VIRUS RESISTANCE TO 2',3'-DIDEOXYCYTIDINE AND 2',3'-DIDEOXY-3'-THIACYTIDINE [J].
GU, ZX ;
GAO, Q ;
FANG, HS ;
SALOMON, H ;
PARNIAK, MA ;
GOLDBERG, E ;
CAMERON, J ;
WAINBERG, MA .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 1994, 38 (02) :275-281
[6]   INHIBITORY EFFECTS OF ACYCLIC NUCLEOSIDE PHOSPHONATES ON HUMAN HEPATITIS-B VIRUS AND DUCK HEPATITIS-B VIRUS-INFECTIONS IN TISSUE-CULTURE [J].
HEIJTINK, RA ;
KRUINING, J ;
DEWILDE, GA ;
BALZARINI, J ;
DECLERCQ, E ;
SCHALM, SW .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 1994, 38 (09) :2180-2182
[7]   Human immunodeficiency virus type 1 expressing the lamivudine-associated M184V mutation in reverse transcriptase shows increased susceptibility to adefovir and decreased replication capability in vitro [J].
Miller, MD ;
Anton, KE ;
Mulato, AS ;
Lamy, PD ;
Cherrington, JM .
JOURNAL OF INFECTIOUS DISEASES, 1999, 179 (01) :92-100
[8]  
Schooley R, 2000, 40 INT C ANT AG CHEM
[9]   Combination of mutations in human immunodeficiency virus type 1 reverse transcriptase required for resistance to the carbocyclic nucleoside 1592U89 [J].
Tisdale, M ;
Alnadaf, T ;
Cousens, D .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 1997, 41 (05) :1094-1098
[10]  
Wainberg MA, 1999, ANTIVIR THER, V4, P87