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抗体偶联药物一剂即可治愈一期非洲锥虫病模型。

A single dose of antibody-drug conjugate cures a stage 1 model of African trypanosomiasis.

机构信息

Department of Biochemistry, University of Cambridge, Cambridge, United Kingdom.

Department of Antibody Discovery and Protein Engineering, Medimmune, Cambridge, United Kingdom.

出版信息

PLoS Negl Trop Dis. 2019 May 23;13(5):e0007373. doi: 10.1371/journal.pntd.0007373. eCollection 2019 May.

Abstract

Infections of humans and livestock with African trypanosomes are treated with drugs introduced decades ago that are not always fully effective and often have severe side effects. Here, the trypanosome haptoglobin-haemoglobin receptor (HpHbR) has been exploited as a route of uptake for an antibody-drug conjugate (ADC) that is completely effective against Trypanosoma brucei in the standard mouse model of infection. Recombinant human anti-HpHbR monoclonal antibodies were isolated and shown to be internalised in a receptor-dependent manner. Antibodies were conjugated to a pyrrolobenzodiazepine (PBD) toxin and killed T. brucei in vitro at picomolar concentrations. A single therapeutic dose (0.25 mg/kg) of a HpHbR antibody-PBD conjugate completely cured a T. brucei mouse infection within 2 days with no re-emergence of infection over a subsequent time course of 77 days. These experiments provide a demonstration of how ADCs can be exploited to treat protozoal diseases that desperately require new therapeutics.

摘要

人体和家畜感染非洲锥虫病的治疗方法是使用几十年前引入的药物,但这些药物并不总是完全有效,而且往往有严重的副作用。在这里,锥虫触珠蛋白-血红蛋白受体 (HpHbR) 被用作抗体药物偶联物 (ADC) 的摄取途径,该 ADC 在感染的标准小鼠模型中对布氏锥虫完全有效。分离出重组人抗 HpHbR 单克隆抗体,并证明其以受体依赖性方式内化。将抗体与吡咯并苯二氮杂卓 (PBD) 毒素缀合,并在皮摩尔浓度下在体外杀死 T. brucei。单次治疗剂量 (0.25 mg/kg) 的 HpHbR 抗体-PBD 缀合物在 2 天内即可完全治愈 T. brucei 小鼠感染,随后 77 天内无感染再次出现。这些实验证明了如何利用 ADC 来治疗迫切需要新疗法的原生动物疾病。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5e18/6532856/d436b6fb32b7/pntd.0007373.g001.jpg

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