首页> 美国卫生研究院文献>Antimicrobial Agents and Chemotherapy >Antiviral efficacy in vivo of the anti-human immunodeficiency virus bicyclam SDZ SID 791 (JM 3100) an inhibitor of infectious cell entry.
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Antiviral efficacy in vivo of the anti-human immunodeficiency virus bicyclam SDZ SID 791 (JM 3100) an inhibitor of infectious cell entry.

机译:抗人免疫缺陷病毒bicyclam SDZ SID 791(JM 3100)(一种感染性细胞进入的抑制剂)的体内抗病毒效力。

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摘要

SID 791, a bicyclam inhibiting human immunodeficiency virus (HIV) replication in vitro by blocking virus entry into cells, is an effective inhibitor of virus production and of depletion of human CD4+ T cells in HIV type 1-infected SCID-hu Thy/Liv mice. Steady levels of 100 ng of SID 791 or higher per ml in plasma resulted in statistically significant inhibition of p24 antigen formation. Daily injections of SID 791 caused a dose-dependent decrease in viremia, and this inhibition could be potentiated by coadministration of zidovudine or didanose. The present study suggests that SID 791 alone or in combination with licensed antiviral agents may decrease the virus load in HIV-infected patients and, by extension, that the infectious cell entry step is a valid target for antiviral chemotherapy of HIV disease. The SCID-hu Thy/Liv model in effect provides a rapid means of assessing the potential of compounds with novel modes of antiviral action, as well as the potential of antiviral drug combinations.
机译:SID 791是一种双环素,可通过阻止病毒进入细胞来在体外抑制人免疫缺陷病毒(HIV)的复制,是一种有效的抑制剂,可抑制HIV 1型感染的SCID-hu Thy / Liv小鼠体内的病毒产生和人CD4 + T细胞的消耗。血浆中每毫升100 ng SID 791或更高的稳定水平导致p24抗原形成的统计学显着抑制。每天注射SID 791会引起病毒血症剂量依赖性的下降,齐多夫定或双糖的共同给药可增强这种抑制作用。本研究表明,单独使用SID 791或与许可的抗病毒剂联合使用,可以降低HIV感染患者的病毒载量,并且通过扩展,传染性细胞进入步骤是HIV疾病抗病毒化学疗法的有效靶标。实际上,SCID-hu Thy / Liv模型提供了一种快速的方法来评估具有新型抗病毒作用模式的化合物的潜力以及抗病毒药物组合的潜力。

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