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基于二维气道类器官筛选系统的 SARS-CoV-2 RBD 靶向多克隆治疗性抗体的产生和效果测试。

Generation and Effect Testing of a SARS-CoV-2 RBD-Targeted Polyclonal Therapeutic Antibody Based on a 2-D Airway Organoid Screening System.

机构信息

School of Medicine, Southern University of Science and Technology, Shenzhen, China.

Institute of Biomedicine and Biotechnology, Shenzhen Institute of Advanced Technology, Chinese Academy of Sciences, Shenzhen, China.

出版信息

Front Immunol. 2021 Oct 18;12:689065. doi: 10.3389/fimmu.2021.689065. eCollection 2021.

Abstract

Coronavirus disease 2019 (COVID-19) is an acute respiratory infectious disease caused by infection with severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2). The US FDA has approved several therapeutics and vaccines worldwide through the emergency use authorization in response to the rapid spread of COVID-19. Nevertheless, the efficacies of these treatments are being challenged by viral escape mutations. There is an urgent need to develop effective treatments protecting against SARS-CoV-2 infection and to establish a stable effect-screening model to test potential drugs. Polyclonal antibodies (pAbs) have an intrinsic advantage in such developments because they can target rapidly mutating viral strains as a result of the complexity of their binding epitopes. In this study, we generated anti-receptor-binding domain (anti-RBD) pAbs from rabbit serum and tested their safety and efficacy in response to SARS-CoV-2 infection both and . Primary human bronchial epithelial two-dimensional (2-D) organoids were cultured and differentiated to a mature morphology and subsequently employed for SARS-CoV-2 infection and drug screening. The pAbs protected the airway organoids from viral infection and tissue damage. Potential side effects were tested in mouse models for both inhalation and vein injection. The pAbs displayed effective viral neutralization effects without significant side effects. Thus, the use of animal immune serum-derived pAbs might be a potential therapy for protection against SARS-CoV-2 infection, with the strategy developed to produce these pAbs providing new insight into the treatment of respiratory tract infections, especially for infections with viruses undergoing rapid mutation.

摘要

新型冠状病毒病(COVID-19)是由严重急性呼吸综合征冠状病毒 2(SARS-CoV-2)感染引起的急性呼吸道传染病。美国食品药品监督管理局(FDA)通过紧急使用授权在全球范围内批准了几种治疗药物和疫苗,以应对 COVID-19 的快速传播。然而,这些治疗方法的疗效受到病毒逃逸突变的挑战。迫切需要开发针对 SARS-CoV-2 感染的有效治疗方法,并建立稳定的效应筛选模型来测试潜在药物。多克隆抗体(pAbs)在这些开发中具有内在优势,因为它们可以针对由于其结合表位的复杂性而快速突变的病毒株。在这项研究中,我们从兔血清中产生了针对受体结合域(anti-RBD)的 pAbs,并测试了它们对 SARS-CoV-2 感染的安全性和疗效。原代人支气管上皮二维(2-D)类器官被培养和分化为成熟形态,随后用于 SARS-CoV-2 感染和药物筛选。pAbs 保护气道类器官免受病毒感染和组织损伤。在吸入和静脉注射的小鼠模型中测试了潜在的副作用。pAbs 显示出有效的病毒中和作用,没有明显的副作用。因此,使用动物免疫血清衍生的 pAbs 可能是预防 SARS-CoV-2 感染的潜在治疗方法,所开发的产生这些 pAbs 的策略为治疗呼吸道感染提供了新的思路,特别是对于正在发生快速突变的病毒感染。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/03e3/8559598/0dbcec7f6958/fimmu-12-689065-g001.jpg

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