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新型硫酸化聚合物作为人类免疫缺陷病毒复制和巨细胞形成的高效选择性抑制剂。

Novel sulfated polymers as highly potent and selective inhibitors of human immunodeficiency virus replication and giant cell formation.

作者信息

Baba M, Schols D, De Clercq E, Pauwels R, Nagy M, Györgyi-Edelényi J, Löw M, Görög S

机构信息

Rega Institute for Medical Research, Katholieke Universiteit Leuven, Belgium.

出版信息

Antimicrob Agents Chemother. 1990 Jan;34(1):134-8. doi: 10.1128/AAC.34.1.134.

Abstract

Novel synthetic sulfated polymers, namely, sulfated polyvinyl alcohol (PVAS) and sulfated copolymers of acrylic acid with vinyl alcohol (PAVAS), proved to be potent and selective inhibitors of human immunodeficiency virus type 1 (HIV-1) and HIV-2 in vitro. The compounds completely inhibited HIV-1-induced cytopathogenicity in MT-4 cells and HIV-1 antigen expression in CEM cells at a concentration of 0.8 micrograms/ml. They were equally effective against HIV-2 replication. In addition, and in contrast to azidothymidine, PAVAS and PVAS suppressed HIV-1-induced giant cell (syncytium) formation, a process that may account for the depletion of T4 lymphocytes in patients with acquired immunodeficiency syndrome. PAVAS and PVAS completely blocked giant cell formation at a concentration of 4 micrograms/ml, whereas for dextran sulfate a concentration of 100 micrograms/ml was required to achieve complete inhibition of giant cell formation. As has been demonstrated previously for the sulfated polysaccharides, the mechanism of action of PAVAS and PVAS resides in the inhibition of virus adsorption to the cells.

摘要

新型合成硫酸化聚合物,即硫酸化聚乙烯醇(PVAS)和丙烯酸与乙烯醇的硫酸化共聚物(PAVAS),在体外被证明是1型人类免疫缺陷病毒(HIV-1)和HIV-2的强效且选择性抑制剂。这些化合物在浓度为0.8微克/毫升时能完全抑制MT-4细胞中HIV-1诱导的细胞病变效应以及CEM细胞中HIV-1抗原的表达。它们对HIV-2复制同样有效。此外,与叠氮胸苷不同的是,PAVAS和PVAS抑制HIV-1诱导的巨细胞(多核细胞)形成,这一过程可能是获得性免疫缺陷综合征患者T4淋巴细胞耗竭的原因。PAVAS和PVAS在浓度为4微克/毫升时能完全阻断巨细胞形成,而对于硫酸葡聚糖,则需要100微克/毫升的浓度才能完全抑制巨细胞形成。正如先前对硫酸化多糖所证明的那样,PAVAS和PVAS的作用机制在于抑制病毒吸附到细胞上。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5e76/171534/702f2fc4241a/aac00057-0168-a.jpg

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