In vitro determination of antiviral activity of MSS209, a new amphotericin B derivative, against primary isolates of HIV1

被引:5
作者
MagierowskaJung, M
Cefai, D
Marrakchi, H
Chieze, F
Agut, H
Huraux, JM
Seman, M
机构
[1] DANA FARBER CANC INST,DIV TUMOR IMMUNOL,IMMUNOL LAB,BOSTON,MA 02115
[2] UNIV PARIS 07,LAB IMMUNODIFFERENCIAT,F-75251 PARIS 05,FRANCE
[3] HOP LA PITIE SALPETRIERE,INSERM U313,DEPT MALAD INFECT PARASITAIRES TROP & SANTE PUBL,F-75651 PARIS 13,FRANCE
来源
RESEARCH IN VIROLOGY | 1996年 / 147卷 / 05期
关键词
HIV1; amphotericin B; derivative MS8209; antiviral activity; primary isolates;
D O I
10.1016/0923-2516(96)82289-8
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
MS8209. an amphotericin B derivative, was previously reported to be an inhibitor of HIV1 replication in vitro. In the present study, we determined the 50 and 90% in vitro inhibitory concentrations of MS8209 for 9 HIV1 isolates including both zidovudine-sensitive and zidovudine-resistant isolates and the reference strain Lai, using the peripheral blood mononuclear cell (PBMC) assay. We also evaluated the sensitivity of HIV1 replication to MS8209 during primary isolation from PBMCs. An inhibitory effect of MS8209 in PBMC infection was observed either when the drug was only present during the adsorption step or when the drug was initially absent but maintained throughout the culture period; the combination of these two approaches provided the highest inhibition rate. These results indicate that MS8209 can inhibit the replication of HIV1 isolates in PBMCs and suggest that it mainly acts by blocking the virus entry into cells.
引用
收藏
页码:313 / 318
页数:6
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