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强效中和抗体对致死性埃博拉病毒感染的保护性单药治疗。

Protective monotherapy against lethal Ebola virus infection by a potently neutralizing antibody.

机构信息

Institute for Research in Biomedicine, Università della Svizzera Italiana, CH-6500 Bellinzona, Switzerland. Humabs BioMed SA, 6500 Bellinzona, Switzerland.

Vaccine Research Center, National Institute of Allergy and Infectious Diseases, Bethesda, MD 20892, USA.

出版信息

Science. 2016 Mar 18;351(6279):1339-42. doi: 10.1126/science.aad5224. Epub 2016 Feb 25.

Abstract

Ebola virus disease in humans is highly lethal, with case fatality rates ranging from 25 to 90%. There is no licensed treatment or vaccine against the virus, underscoring the need for efficacious countermeasures. We ascertained that a human survivor of the 1995 Kikwit Ebola virus disease outbreak maintained circulating antibodies against the Ebola virus surface glycoprotein for more than a decade after infection. From this survivor we isolated monoclonal antibodies (mAbs) that neutralize recent and previous outbreak variants of Ebola virus and mediate antibody-dependent cell-mediated cytotoxicity in vitro. Strikingly, monotherapy with mAb114 protected macaques when given as late as 5 days after challenge. Treatment with a single human mAb suggests that a simplified therapeutic strategy for human Ebola infection may be possible.

摘要

人类埃博拉病毒病具有极高的致死率,病死率范围为 25%至 90%。目前尚无针对该病毒的许可治疗方法或疫苗,这凸显了开发有效应对措施的必要性。我们确认,一位曾于 1995 年基奎特埃博拉病毒病疫情中幸存的人类患者,在感染后超过十年的时间里仍保持针对埃博拉病毒表面糖蛋白的循环抗体。从该幸存者中,我们分离出了单克隆抗体(mAb),这些 mAb 能够中和近期和以往埃博拉病毒爆发的变异株,并在体外介导抗体依赖的细胞介导的细胞毒性。引人注目的是,mAb114 单药治疗在挑战后 5 天给予时即可保护猕猴。单一人类 mAb 的治疗表明,针对人类埃博拉病毒感染的简化治疗策略可能是可行的。

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