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具有广泛口蹄疫病毒株识别能力的新型衣壳特异性单域抗体揭示了病毒粒子、空衣壳和病毒样颗粒的抗原性差异。

Novel Capsid-Specific Single-Domain Antibodies with Broad Foot-and-Mouth Disease Strain Recognition Reveal Differences in Antigenicity of Virions, Empty Capsids, and Virus-Like Particles.

作者信息

Li Haozhou, Dekker Aldo, Sun Shiqi, Burman Alison, Kortekaas Jeroen, Harmsen Michiel M

机构信息

Laboratory of Virology, Wageningen University and Research, 6708 PB Wageningen, The Netherlands.

State Key Laboratory of Veterinary Etiological Biology and National Foot and Mouth Disease Reference Laboratory, Lanzhou Veterinary Research Institute, Chinese Academy of Agricultural Sciences, Lanzhou 730046, China.

出版信息

Vaccines (Basel). 2021 Jun 8;9(6):620. doi: 10.3390/vaccines9060620.

Abstract

Foot-and-mouth disease (FMD) vaccine efficacy is mainly determined by the content of intact virions (146S) and empty capsids (75S). Both particles may dissociate into 12S subunits upon vaccine manufacturing, formulation, and storage, reducing vaccine potency. We report the isolation of capsid-specific llama single-domain antibodies (VHHs) with broad strain recognition that can be used to quantify intact capsids in FMD vaccines by double antibody sandwich (DAS) ELISA. One capsid-specific VHH displayed remarkably broad strain reactivity, recognizing 14 strains representing the 13 most important lineages of serotype A, and two VHHs cross-reacted with other serotypes. We additionally show that the newly isolated VHHs, as well as previously characterized VHHs, can be used to identify antigenic differences between authentic 146S and 75S capsids, as well as corresponding genetically engineered virus-like particles (VLPs). Our work underscores that VHHs are excellent tools for monitoring the quantity and stability of intact capsids during vaccine manufacturing, formulation, and storage, and additionally shows that VHHs can be used to predict the native-like structure of VLPs.

摘要

口蹄疫(FMD)疫苗的效力主要由完整病毒粒子(146S)和空衣壳(75S)的含量决定。在疫苗生产、配方和储存过程中,这两种颗粒都可能解离成12S亚基,从而降低疫苗效力。我们报告了具有广泛毒株识别能力的衣壳特异性骆驼单域抗体(VHHs)的分离,这些抗体可用于通过双抗体夹心(DAS)ELISA定量FMD疫苗中的完整衣壳。一种衣壳特异性VHH表现出显著广泛的毒株反应性,可识别代表血清型A的13个最重要谱系的14种毒株,并且两种VHH与其他血清型发生交叉反应。我们还表明,新分离的VHH以及先前表征的VHH可用于识别真实的146S和75S衣壳以及相应的基因工程病毒样颗粒(VLPs)之间的抗原差异。我们的工作强调,VHH是在疫苗生产、配方和储存过程中监测完整衣壳数量和稳定性的优秀工具,此外还表明VHH可用于预测VLPs的天然样结构。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1abf/8227720/5e7783f01bfb/vaccines-09-00620-g001.jpg

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