Zeolitic imidazolate frameworks activate endosomal Toll-like receptors and potentiate immunogenicity of SARS-CoV-2 spike protein trimer
沸石咪唑酯骨架激活内体Toll样受体并增强SARS-CoV-2刺突蛋白三聚体的免疫原性
阅读:1
作者:Shahad K Alsaiari ,Seba Nadeef ,John L Daristotle ,William Rothwell ,Bujie Du ,Johnny Garcia ,Linzixuan Zhang ,Morteza Sarmadi ,Timothy A Forster ,Nandita Menon ,Stacey Qiaohui Lin ,Lisa H Tostanoski ,Nicole Hachmann ,Erika Yan Wang ,John D Ventura ,Dan H Barouch ,Robert Langer ,Ana Jaklenec
| 期刊: | Science Advances | 影响因子: | 11.700 |
| 时间: | 2024 | 起止号: | 2024 Mar 8;10(10):eadj6380. |
| doi: | 10.1126/sciadv.adj6380 | 种属: | Rabbit |
| 靶点: | IgG | 研究方向: | 代谢、信号转导、免疫、心血管 |
| 疾病类型: | 新冠 | 信号通路: | Toll-Like Receptor |
Abstract
Nanomaterials offer unique opportunities to engineer immunomodulatory activity. In this work, we report the Toll-like receptor agonist activity of a nanoscale adjuvant zeolitic imidazolate framework-8 (ZIF-8). The accumulation of ZIF-8 in endosomes and the pH-responsive release of its subunits enable selective engagement with endosomal Toll-like receptors, minimizing the risk of off-target activation. The intrinsic adjuvant properties of ZIF-8, along with the efficient delivery and biomimetic presentation of a severe acute respiratory syndrome coronavirus 2 spike protein receptor-binding domain trimer, primed rapid humoral and cell-mediated immunity in a dose-sparing manner. Our study offers insights for next-generation adjuvants that can potentially impact future vaccine development.
特别声明
1、本页面内容包含部分的内容是基于公开信息的合理引用;引用内容仅为补充信息,不代表本站立场。
2、若认为本页面引用内容涉及侵权,请及时与本站联系,我们将第一时间处理。
3、其他媒体/个人如需使用本页面原创内容,需注明“来源:[生知库]”并获得授权;使用引用内容的,需自行联系原作者获得许可。
4、投稿及合作请联系:info@biocloudy.com。