严重急性呼吸综合征冠状病毒2型(SARS-CoV-2)
2019年冠状病毒病(COVID-19)
2019-20冠状病毒爆发
纳米颗粒
医学
病毒学
纳米技术
材料科学
病理
传染病(医学专业)
爆发
疾病
作者
Yongbo Jiang,Mrinmoy Sanyal,Noor Hussein,Ani Baghdasaryan,Mengzhen Zhang,Feifei Wang,Fuqiang Ren,Jiachen Li,Guanzhou Zhu,Yifan Meng,Julia Z. Adamska,Elizabeth Mellins,Tiancheng Liu
出处
期刊:Science Advances
[American Association for the Advancement of Science]
日期:2025-02-07
卷期号:11 (6)
标识
DOI:10.1126/sciadv.adp5539
摘要
The COVID-19 pandemic caused a global health crisis that resulted in millions of deaths. Effective vaccines have played central roles in curtailing the pandemic. Here, we developed a down-converting near-infrared IIb (NIR-IIb; 1500 to 1700 nanometers) luminescent, pure NaErF4@NaYF4 rare-earth nanoparticle (pEr) as vaccine carriers. The pEr nanoparticles were coated with three layers of cross-linked biocompatible polymers (pEr-P3; ~55 nanometers) and conjugated to the receptor binding domain (RBD) of the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) spike protein. Upon subcutaneous injection of the pEr-P3-RBD nanovaccine in mice, in vivo NIR-IIb imaging revealed active vaccine trafficking and migration to lymph nodes through lymphatic vessels. Two doses of the adjuvant-free vaccine elicited long-lasting (>7 months) high titers of serum viral neutralization antibody and anti-RBD immunoglobulin G, along with robust RBD-specific germinal center B cells and T follicular helper cells. We devised in vivo NIR-II molecular imaging of RBD-specific cells in lymph nodes, opening noninvasive assessments of vaccine-elicited immune responses longitudinally.
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