Department of Radioimmunology, Institute of Radiopharmaceutical Cancer Research, Helmholtz-Zentrum Dresden-Rossendorf (HZDR), Dresden, Germany.
Mildred Scheel Early Career Center, Faculty of Medicine Carl Gustav Carus, Technische Universität Dresden, Dresden, Germany.
Front Immunol. 2023 Jun 13;14:1204543. doi: 10.3389/fimmu.2023.1204543. eCollection 2023.
The coronavirus disease 2019 (COVID-19) pandemic caused by severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) led to millions of infections and deaths worldwide. As this virus evolves rapidly, there is a high need for treatment options that can win the race against new emerging variants of concern. Here, we describe a novel immunotherapeutic drug based on the SARS-CoV-2 entry receptor ACE2 and provide experimental evidence that it cannot only be used for (i) neutralization of SARS-CoV-2 and in SARS-CoV-2-infected animal models but also for (ii) clearance of virus-infected cells. For the latter purpose, we equipped the ACE2 decoy with an epitope tag. Thereby, we converted it to an adapter molecule, which we successfully applied in the modular platforms UniMAB and UniCAR for retargeting of either unmodified or universal chimeric antigen receptor-modified immune effector cells. Our results pave the way for a clinical application of this novel ACE2 decoy, which will clearly improve COVID-19 treatment.
由严重急性呼吸系统综合症冠状病毒 2 型(SARS-CoV-2)引起的 2019 年冠状病毒病(COVID-19)大流行导致了全球数以百万计的感染和死亡。由于这种病毒迅速进化,因此非常需要能够与新出现的令人关注的变异病毒竞争的治疗选择。在这里,我们描述了一种基于 SARS-CoV-2 进入受体 ACE2 的新型免疫治疗药物,并提供了实验证据,表明它不仅可用于(i)中和 SARS-CoV-2 和 SARS-CoV-2 感染的动物模型,还可用于(ii)清除病毒感染的细胞。为此目的,我们在 ACE2 诱饵上配备了一个表位标签。由此,我们将其转化为一种衔接分子,并成功地将其应用于 UniMAB 和 UniCAR 这两个模块化平台,用于重新靶向未经修饰或通用嵌合抗原受体修饰的免疫效应细胞。我们的结果为这种新型 ACE2 诱饵的临床应用铺平了道路,这将明显改善 COVID-19 的治疗。