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一种抗病毒黄原酸盐化合物在体外对HIV-1复制的抑制作用。

Inhibition of HIV-1 replication by an antiviral xanthate compound in vitro.

作者信息

Mellert W, Amtmann E, Erfle V, Sauer G

机构信息

Abt. für Molekulare Zellpathologie, Gesellschaft für Strahlen und Umweltforschung (GSF), Neuherberg/München, West Germany.

出版信息

AIDS Res Hum Retroviruses. 1988 Feb;4(1):71-81. doi: 10.1089/aid.1988.4.71.

Abstract

The antiviral xanthate compound tricyclodecan-9-yl-xanthogenate (code name D609) is capable of inhibiting DNA and RNA viruses in vitro. It can also inhibit the shedding of infectious HIV into the tissue culture medium from chronically infected lymphoma cells (KE37-III) as shown by infectivity assays and Western blots of the supernatant. HIV-specific proteins, however, were accumulated intracellularly. The initiation of a de novo HIV replication after infection of permissive KE37-1 cells was completely inhibited at concentrations of D609 which still permitted mitotic divisions of the cells. Furthermore, the selective antiviral activity of the xanthate compound was evidenced by the absence of HIV replicative intermediate DNA. The expression of cellular genes, such as c-myc, remained unimpaired within these cells.

摘要

抗病毒黄原酸盐化合物三环癸烷-9-基黄原酸酯(代号D609)在体外能够抑制DNA和RNA病毒。如通过上清液的感染性测定和蛋白质免疫印迹所示,它还能抑制慢性感染的淋巴瘤细胞(KE37-III)将传染性HIV释放到组织培养基中。然而,HIV特异性蛋白在细胞内积累。在D609浓度下,允许KE37-1细胞进行有丝分裂的同时,却能完全抑制HIV感染允许性KE37-1细胞后从头开始的HIV复制。此外,黄原酸盐化合物的选择性抗病毒活性通过不存在HIV复制中间DNA得以证明。在这些细胞内,诸如c-myc等细胞基因的表达未受损害。

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