Phenylarsine oxide inhibits ex vivo HIV-1 expression

被引:16
作者
Arbault, S
Edeas, M
Legrand-Poels, S
Sojic, N
Amatore, C
Piette, J
Best-Belpomme, M
Lindenbaum, A
Vuillaume, M
机构
[1] Ecole Normale Super, URA 1679, F-75231 Paris 05, France
[2] Ecole Normale Super, UPR42 CNRS, F-75231 Paris, France
[3] Hop Antoine Beclere, Biochim Lab, F-92141 Clamart, France
[4] Univ Paris 06, URA 1135 CNRS, F-75005 Paris, France
[5] Univ Liege, Virol Lab, B-4000 Liege, Belgium
关键词
phenylarsine oxide; HIV-1; expression; PMA; TNF-alpha; NF-kappa B inactivation;
D O I
10.1016/S0753-3322(97)82321-9
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Phenylarsine oxide (PAO), which is described as an inhibitor of tyrosine phosphatase activity, inhibits H2O2 release from human peripheral blood mononuclear cells (PBMCs) as measured by electrochemistry. Since human immunodeficiency virus type 1 (HIV-1) replication is known to be favored under oxidative stress conditions, ex vivo experiments using uninfected PBMCs, primary monocytes or a latently infected promonocytic U1 cell line show that HIV-1 replication and reactivation, monitored by p24 antigen measurement, are inhibited by PAO in a time- and concentration-dependent manner. These observations can be linked with the inhibition of NF-kappa B activation when uninfected monocytes are induced by either tumor necrosis factor alpha (TNF-a), phurbol 12-myristate 13-acetate (PMA) or lipopolysaccharide (LPS).
引用
收藏
页码:430 / 438
页数:9
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