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Article: A SARS-CoV-2 vaccine on an NIR-II/SWIR emitting nanoparticle platform

TitleA SARS-CoV-2 vaccine on an NIR-II/SWIR emitting nanoparticle platform
Authors
Issue Date7-Feb-2025
PublisherAmerican Association for the Advancement of Science
Citation
Science Advances, 2025, v. 11, n. 6 How to Cite?
AbstractThe 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.
Persistent Identifierhttp://hdl.handle.net/10722/361998

 

DC FieldValueLanguage
dc.contributor.authorJiang, Yingying-
dc.contributor.authorSanyal, Mrinmoy-
dc.contributor.authorHussein, Noor A.-
dc.contributor.authorBaghdasaryan, Ani-
dc.contributor.authorZhang, Mengzhen-
dc.contributor.authorWang, Feifei-
dc.contributor.authorRen, Fuqiang-
dc.contributor.authorLi, Jiachen-
dc.contributor.authorZhu, Guanzhou-
dc.contributor.authorMeng, Yifan-
dc.contributor.authorAdamska, Julia Zofia-
dc.contributor.authorMellins, Elizabeth-
dc.contributor.authorDai, Hongjie-
dc.date.accessioned2025-09-18T00:36:08Z-
dc.date.available2025-09-18T00:36:08Z-
dc.date.issued2025-02-07-
dc.identifier.citationScience Advances, 2025, v. 11, n. 6-
dc.identifier.urihttp://hdl.handle.net/10722/361998-
dc.description.abstractThe 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.-
dc.languageeng-
dc.publisherAmerican Association for the Advancement of Science-
dc.relation.ispartofScience Advances-
dc.rightsThis work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License.-
dc.titleA SARS-CoV-2 vaccine on an NIR-II/SWIR emitting nanoparticle platform-
dc.typeArticle-
dc.identifier.doi10.1126/sciadv.adp5539-
dc.identifier.pmid39919189-
dc.identifier.scopuseid_2-s2.0-85218113832-
dc.identifier.volume11-
dc.identifier.issue6-
dc.identifier.eissn2375-2548-
dc.identifier.issnl2375-2548-

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