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多聚体单域抗体复合物可预防布尼亚病毒感染。

Multimeric single-domain antibody complexes protect against bunyavirus infections.

机构信息

Department of Virology, Wageningen Bioveterinary Research, Lelystad, Netherlands.

Laboratory of Virology, Wageningen University, Wageningen, Netherlands.

出版信息

Elife. 2020 Apr 21;9:e52716. doi: 10.7554/eLife.52716.

Abstract

The World Health Organization has included three bunyaviruses posing an increasing threat to human health on the Blueprint list of viruses likely to cause major epidemics and for which no, or insufficient countermeasures exist. Here, we describe a broadly applicable strategy, based on llama-derived single-domain antibodies (VHHs), for the development of bunyavirus biotherapeutics. The method was validated using the zoonotic Rift Valley fever virus (RVFV) and Schmallenberg virus (SBV), an emerging pathogen of ruminants, as model pathogens. VHH building blocks were assembled into highly potent neutralizing complexes using bacterial superglue technology. The multimeric complexes were shown to reduce and prevent virus-induced morbidity and mortality in mice upon prophylactic administration. Bispecific molecules engineered to present two different VHHs fused to an Fc domain were further shown to be effective upon therapeutic administration. The presented VHH-based technology holds great promise for the development of bunyavirus antiviral therapies.

摘要

世界卫生组织已将三种对人类健康构成日益严重威胁的布尼亚病毒列入蓝图清单,这些病毒可能引发重大疫情,但目前尚无针对它们的对策,或者对策不足。在这里,我们描述了一种基于羊驼衍生的单域抗体(VHH)的广泛适用的布尼亚病毒生物治疗策略。该方法已使用人畜共患裂谷热病毒(RVFV)和沙氏门菌病毒(SBV)得到验证,这两种病毒分别是新兴的反刍动物病原体和人类病原体。使用细菌超强胶技术将 VHH 构建块组装成高效的中和复合物。实验表明,在预防性给药时,多聚体复合物可降低和预防病毒引起的发病率和死亡率。双特异性分子经工程设计可融合两个不同的 VHH 到 Fc 结构域,在治疗性给药时也显示出有效性。所提出的基于 VHH 的技术为开发布尼亚病毒抗病毒疗法提供了巨大的潜力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6ca3/7173960/925184cc77aa/elife-52716-fig1.jpg

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