The bis-azo compound FP-21399 inhibits HIV-1 replication by preventing viral entry

被引:23
作者
Zhang, JL
Choe, H
Dezube, BJ
Farzan, M
Sharma, PL
Zhou, XC
Chen, LB
Ono, M
Gillies, S
Wu, YM
Sodroski, JG
Crumpacker, CS
机构
[1] Beth Israel Deaconess Med Ctr, Div Infect Dis, Boston, MA 02215 USA
[2] Beth Israel Deaconess Med Ctr, Div Hematol Oncol, Boston, MA 02215 USA
[3] Dana Farber Canc Inst, Div Human Retrovirol, Boston, MA 02115 USA
[4] Dana Farber Canc Inst, Div Cellular & Mol Biol, Boston, MA 02115 USA
[5] Fuji ImmunoPharmaceut Corp, Lexington, MA 02173 USA
关键词
D O I
10.1006/viro.1998.9115
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
The bis-azo compound FP-21399 inhibits HIV-1 infection. We now show that FP-21399 acts on the HIV-1 envelope glycoprotein to prevent viral replication. This compound targets the entry step of the HIV-1 replication cycle as demonstrated by time-of-addition and single cycle viral entry assays. The entry of SIV(mac)239, which uses the same coreceptors (CD4/CCR5) as HIV-1, was not inhibited by FP-21399, indicating that the antiviral effect of FP-21399 is specific for the HIV-1 envelope glycoprotein and is not dependent upon the cellular receptors CD4 and CCR5. FP-21399 inhibits neither the activity of HIV-1 reverse transcriptase nor the expression of HIV-1 early mRNA. Finally, this compound inhibits gp120 shedding of the T-tropic virus. Our results suggest that the anti-HIV activity of FP-21399 is due to its interaction with HIV-1 gp120/41 complex during viral entry. (C) 1998 Academic Press.
引用
收藏
页码:530 / 541
页数:12
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