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化脓性链球菌制剂OK-432对单纯疱疹病毒致死性感染小鼠的保护作用。

Protection of OK-432, a Streptococcus pyogenes preparation, against lethal infection of mice with herpes simplex virus.

作者信息

Harada Y, Kurokawa E, Endo H, Kimura T, Saito M, Sugawara Y, Irie H, Ito K, Fujii M, Shimizu Y

机构信息

Research Laboratories, Chugai Pharmaceutical Co., Ltd., Tokyo.

出版信息

Microbiol Immunol. 1989;33(6):467-77. doi: 10.1111/j.1348-0421.1989.tb01996.x.

Abstract

We have studied the protective effect of OK-432, a biological response modifier (BRM) of Streptococcus pyogenes origin, on the lethal infection of mice with herpes simplex virus (HSV)-1. A single intraperitoneal (i.p.) injection of more than 10 micrograms of OK-432, when given at least two days before the infection, gave a marked effect yielding nearly 100% protection against ordinarily lethal infection. The protection was independent of the amount of infected virus inoculated. When given after the infection, the agent even at the maximal dose (100 micrograms), produced only a marginal effect. A single i.p. administration of OK-432 augmented the natural killer (NK) activity of peritoneal exudate cells and spleen mononuclear cells in mice 2 to 3 days after injection of OK-432, coinciding with the times when it induced a survival effect on HSV-infection. Treating OK-432-treated mice with a combination of an anti-macrophage agent, silica, and an anti-NK cell agent, anti-asialo GM1 serum, before infection diminished the antiviral effect of OK-432. The OK-432 protection against HSV infection was also markedly diminished in athymic nude mice. Thus, the protective effect of OK-432 on lethal HSV infection seems to be based on the activation of NK cells, macrophages, and T lymphocytes.

摘要

我们研究了源自化脓性链球菌的生物反应调节剂(BRM)溶链菌制剂(OK-432)对单纯疱疹病毒1型(HSV-1)致死性感染小鼠的保护作用。在感染前至少两天腹腔内(i.p.)单次注射超过10微克的OK-432,可产生显著效果,对通常致死性感染的保护率接近100%。这种保护作用与接种的感染病毒量无关。在感染后给予该制剂,即使是最大剂量(100微克),也仅产生轻微效果。腹腔内单次注射OK-432后2至3天,可增强小鼠腹腔渗出细胞和脾单核细胞的自然杀伤(NK)活性,这与它对HSV感染诱导存活效应的时间一致。在感染前用抗巨噬细胞剂二氧化硅和抗NK细胞剂抗唾液酸GM1血清联合处理经OK-432处理的小鼠,会减弱OK-432的抗病毒作用。在无胸腺裸鼠中,OK-432对HSV感染的保护作用也明显减弱。因此,OK-432对致死性HSV感染的保护作用似乎基于NK细胞、巨噬细胞和T淋巴细胞的激活。

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