首页> 外国专利> COMPOSITION AND METHOD FOR TREATING CORONAVIRUS INFECTION INCLUDING SARS BY ADMINISTRATION OF THERAPEUTICALLY EFFECTIVE AMOUNT OF TYPE I OR TYPE III INTERFERON RECEPTOR AGONIST AND/OR TYPE II INTERFERON RECEPTOR AGONIST

COMPOSITION AND METHOD FOR TREATING CORONAVIRUS INFECTION INCLUDING SARS BY ADMINISTRATION OF THERAPEUTICALLY EFFECTIVE AMOUNT OF TYPE I OR TYPE III INTERFERON RECEPTOR AGONIST AND/OR TYPE II INTERFERON RECEPTOR AGONIST

机译:通过管理I或III型干扰素受体激动剂和/或II型干扰素受体激动剂的治疗有效量来治疗包括SARS在内的冠状病毒感染的组合物和方法

摘要

PURPOSE: A method of treating coronavirus infection including SARS by administration of a therapeutically effective amount of a Type I or Type III interferon receptor agonist and/or a Type II interferon receptor agonist is provided. It is effective in reducing viral load, or reducing the time to viral clearance, or reducing morbidity or mortality in patients suffering from a coronavirus infection. The composition for treating coronavirus infection including SARS contains a Type I or Type III interferon receptor agonist and/or a Type II interferon receptor agonist. CONSTITUTION: The coronavirus infection including SARS is performed by the step of administration of a therapeutically effective amount of IFN-alpha and IFN-gamma to an individual, in which the individual is exposed to coronavirus and the IFN-alpha and IFN-gamma are administered within 24hr, 48hr or 72hr or 35 days. A Type I or III interferon receptor agonist can be administered daily, twice daily, every other day, twice a week, three times a week. Effective dosages of a Type I interferon receptor agonist can range from about 1 to about 180micrograms. The Type I interferon receptor agonist is IFN-alpha. The IFN-alpha and IFN-gamma are administered subcutaneously in multiple doses. The method of treating a coronavirus infection is effective in reducing the risk that an individual will develop a pathological coronavirus infection, which has clinical sequelae.
机译:目的:提供一种通过施用治疗有效量的I型或III型干扰素受体激动剂和/或II型干扰素受体激动剂来治疗包括SARS的冠状病毒感染的方法。它对减少冠状病毒感染患者的病毒载量或缩短病毒清除时间或降低发病率或死亡率有效。包括SARS在内的用于治疗冠状病毒感染的组合物包含I型或III型干扰素受体激动剂和/或II型干扰素受体激动剂。组成:包括SARS的冠状病毒感染是通过向个体施用治疗有效量的IFN-α和IFN-γ的步骤进行的,其中该个体暴露于冠状病毒并给予IFN-α和IFN-γ在24小时,48小时或72小时或35天内。 I型或III型干扰素受体激动剂可以每天,每天两次,隔天一次,一周两次,一周三次给药。 I型干扰素受体激动剂的有效剂量可以在约1至约180微克的范围内。 I型干扰素受体激动剂是IFN-α。 IFN-α和IFN-γ以多次剂量皮下给药。治疗冠状病毒感染的方法可有效降低个体发生具有临床后遗症的病理性冠状病毒感染的风险。

著录项

  • 公开/公告号KR20040088393A

    专利类型

  • 公开/公告日2004-10-16

    原文格式PDF

  • 申请/专利权人 INTERMUNE INC.;

    申请/专利号KR20040022531

  • 发明设计人 BLATT LAWRENCE M.;

    申请日2004-04-01

  • 分类号A61K38/21;

  • 国家 KR

  • 入库时间 2022-08-21 22:47:52

相似文献

  • 专利
  • 外文文献
  • 中文文献
获取专利

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号