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DNA 折纸呈现 SARS-CoV-2 的受体结合域,引发强烈的保护性免疫反应。

DNA origami presenting the receptor binding domain of SARS-CoV-2 elicit robust protective immune response.

机构信息

Department of Bioengineering, George Mason University, Fairfax, VA, 22030, USA.

National Center for Biodefense and Infectious Diseases, George Mason University, Manassas, VA, 20110, USA.

出版信息

Commun Biol. 2023 Mar 23;6(1):308. doi: 10.1038/s42003-023-04689-2.

Abstract

Effective and safe vaccines are invaluable tools in the arsenal to fight infectious diseases. The rapid spreading of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) responsible for the coronavirus disease 2019 pandemic has highlighted the need to develop methods for rapid and efficient vaccine development. DNA origami nanoparticles (DNA-NPs) presenting multiple antigens in prescribed nanoscale patterns have recently emerged as a safe, efficient, and easily scalable alternative for rational design of vaccines. Here, we are leveraging the unique properties of these DNA-NPs and demonstrate that precisely patterning ten copies of a reconstituted trimer of the receptor binding domain (RBD) of SARS-CoV-2 along with CpG adjuvants on the DNA-NPs is able to elicit a robust protective immunity against SARS-CoV-2 in a mouse model. Our results demonstrate the potential of our DNA-NP-based approach for developing safe and effective nanovaccines against infectious diseases with prolonged antibody response and effective protection in the context of a viral challenge.

摘要

有效且安全的疫苗是对抗传染病的有力武器。导致 2019 年冠状病毒病大流行的严重急性呼吸系统综合征冠状病毒 2(SARS-CoV-2)迅速传播,凸显出需要开发快速有效的疫苗开发方法。呈现预定纳米级图案的多种抗原的 DNA 折纸纳米颗粒(DNA-NPs)最近已成为合理设计疫苗的安全、高效且易于扩展的替代方法。在这里,我们利用这些 DNA-NPs 的独特性质,并证明将 SARS-CoV-2 的受体结合域(RBD)的重构三聚体的十个拷贝与 CpG 佐剂精确地上图案化在 DNA-NPs 上,能够在小鼠模型中引发针对 SARS-CoV-2 的强大保护免疫。我们的结果表明,我们的基于 DNA-NP 的方法具有开发针对传染病的安全有效的纳米疫苗的潜力,该疫苗具有延长的抗体反应和在病毒挑战下的有效保护。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/eb01/10036672/214de30c2a69/42003_2023_4689_Fig1_HTML.jpg

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