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抗小核糖核酸病毒疗法的现状

Current status of anti-picornavirus therapies.

作者信息

Barnard Dale L

机构信息

Institute for Antiviral Research, Utah State University, 5600 Old Main Hill, Logan, Utah, 84322-5600, USA.

出版信息

Curr Pharm Des. 2006;12(11):1379-90. doi: 10.2174/138161206776361129.

DOI:10.2174/138161206776361129
PMID:16611122
Abstract

Picornaviruses are important human pathogens causing severe morbidity and some mortality with the potential to cause worldwide crippling disease. Currently, there are few treatments for many of the viruses in the Picornaviridae, For rhinoviruses, there are no approved treatments, although ruprintrivir looks promising in clinical trials and pyridazinyl oxime ethers may prove useful. Poliovirus treatments are needed to supplement the World Health Organization's polio eradication plan in order to treat infections caused by reversion of the attenuated vaccine virus and to supplement vaccine coverage control in polio endemic areas. However, no promising compounds for treatment of poliovirus have been developed due to the efficacy of the vaccines in use. Broad-spectrum inhibitors developed for other picornavirus may be useful for poliovirus infections. Coxsackievirus infections in children and in infants are being treated with pleconaril with some efficacy in reducing mortality and improving recovery, albeit the treatment is often on a compassionate use basis. There are no therapies for echovirus infections. Very little drug discovery research is being done to develop inhibitors for echovirus infections, probably due to the broad-spectrum inhibition exhibited by capsid binding agents and protease inhibitors discovered for treatment of other picornaviruses. For example, pyridazinyl oxime ethers are inhibitory to most echoviruses. Treatments for enterovirus infections are also limited, although in a small clinical trial, milrinone seemed to reduce mortality and improve recovery from EV71-induced pulmonary edema. Thus, these results strongly emphasize the need for the development of potent and nontoxic compounds for the treatment of picornavirus infections.

摘要

微小核糖核酸病毒是重要的人类病原体,可导致严重发病,部分可致死,有可能引发全球性致残疾病。目前,对于许多微小核糖核酸病毒科病毒,治疗方法很少。对于鼻病毒,尚无获批的治疗方法,尽管鲁普立韦林在临床试验中前景看好,哒嗪基肟醚可能也会被证明有用。为补充世界卫生组织的脊髓灰质炎根除计划,需要有治疗脊髓灰质炎病毒的方法,以治疗减毒活疫苗病毒回复突变引起的感染,并在脊髓灰质炎流行地区补充疫苗接种覆盖率控制。然而,由于现有疫苗的有效性,尚未开发出有前景的脊髓灰质炎病毒治疗化合物。为其他微小核糖核酸病毒开发的广谱抑制剂可能对脊髓灰质炎病毒感染有用。儿童和婴儿的柯萨奇病毒感染正在使用普来可那立进行治疗,在降低死亡率和改善恢复方面有一定疗效,尽管这种治疗通常是基于同情用药。目前尚无治疗埃可病毒感染的疗法。针对埃可病毒感染开发抑制剂的药物发现研究很少,可能是因为针对其他微小核糖核酸病毒发现的衣壳结合剂和蛋白酶抑制剂具有广谱抑制作用。例如,哒嗪基肟醚对大多数埃可病毒具有抑制作用。肠道病毒感染的治疗方法也很有限,尽管在一项小型临床试验中,米力农似乎能降低死亡率并改善由EV71引起的肺水肿的恢复情况。因此,这些结果强烈强调需要开发有效且无毒的化合物来治疗微小核糖核酸病毒感染。

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