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9-[(1,3-二羟基-2-丙氧基)甲基]鸟嘌呤与重组干扰素联合对单纯疱疹病毒2型的强效协同抑制作用

Potent synergistic inhibition of herpes simplex virus-2 by 9-[(1, 3-dihydroxy-2-propoxy)methyl]guanine in combination with recombinant interferons.

作者信息

Eppstein D A, Marsh Y V

出版信息

Biochem Biophys Res Commun. 1984 Apr 16;120(1):66-73. doi: 10.1016/0006-291x(84)91414-1.

Abstract

DHPG, an acyclic guanine nucleoside with the structure 9-[(1,3-dihydroxy-2-propoxy)methyl]guanine], showed potent synergism with recombinant alpha or beta interferons and modest synergism with gamma interferon in inhibiting the replication of herpes simplex virus type 2 in vitro. The most potent direct anti-herpes viral synergism was obtained by combination of DHPG and recombinant human interferon-beta-ser17; when combined, doses of each near their separate effective dose50's resulted in almost complete elimination of production of infectious virus within a single viral replication cycle. The anti-herpes viral activity of DHPG-interferon combinations was significantly greater than that obtained with acyclovir-interferon combinations.

摘要

DHPG是一种结构为9-[(1,3-二羟基-2-丙氧基)甲基]鸟嘌呤的无环鸟苷,在体外抑制单纯疱疹病毒2型复制时,它与重组α或β干扰素表现出强效协同作用,与γ干扰素表现出适度协同作用。通过将DHPG与重组人干扰素-β-ser17联合使用,可获得最强效的直接抗疱疹病毒协同作用;联合使用时,各自接近其单独有效剂量50时,在单个病毒复制周期内几乎可完全消除传染性病毒的产生。DHPG-干扰素组合的抗疱疹病毒活性显著高于阿昔洛韦-干扰素组合。

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