错配双链RNA的临床研究。

D R Strayer, W A Carter, I Brodsky, D H Gillespie, J J Greene, P O Ts'o
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引用次数: 0

摘要

在最初的人体试验中,不匹配的诱导剂/激活剂疗法已经显示出明确的临床前景。事实上,错配的dsRNA甚至可能比传统的(外源性)干扰素治疗更有效,原因包括:(a)首先,产生多种干扰素的潜力,从而消除了将特定类型(或亚型)干扰素靶向于特定细胞类型的可能必要性;(b)其次,已知的错配诱导剂能够激活细胞暴露于各种干扰素后合成的细胞内介质;(c)最后,最近证明,诱导剂/激活剂与干扰素联合使用,可以克服细胞对单独干扰素的获得性耐药性(13)。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Clinical studies with mismatched double-stranded RNA.

Mismatched inducer/activator therapy has demonstrated areas of definite clinical promise in its initial human trials. Indeed, the mismatched dsRNA may even prove more efficacious than conventional (exogenous) interferon therapy for several reasons including: (a) First, the potential for generating multiple species of interferons, thereby removing the possible necessity of targeting a specific type (or subtype) of interferon to a particular cell type, (b) Secondly, the known ability of the mismatched inducer to activate the intracellular mediators which are synthesized after cellular exposure to the various types of interferon, (c) Lastly, the recently demonstrated ability of the inducer/activator in combination with interferon to override acquired cellular resistance to interferon alone (13).

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