Cellular Nanoparticles Treat Coronavirus Infection <i>in Vivo</i>
Cellular nanoparticles (CNPs), which refer to nanoparticles coated with natural cell membranes, are promising for neutralizing pathological agents. Here, we use CNPs as a medical countermeasure against the infection of SARS-CoV-2 variants in an animal model. CNPs comprise polymeric cores coated with the plasma membranes of human macrophages. The resulting nanoparticles (MΦ-NPs) act as host cell decoys to intercept SARS-CoV-2 and block its cellular entry, thus inhibiting subsequent viral infection. Our findings indicate that MΦ-NPs bind to the spike proteins of SARS-CoV-2 variants in a dose-dependent manner and inhibit the infectivity of live viruses. In hamsters infected with SARS-CoV-2 variants, MΦ-NPs significantly reduce the viral burden in the lungs, demonstrating their effectiveness in inhibiting viral infectivity <i>in vivo</i>. Furthermore, MΦ-NPs are primarily taken up by alveolar macrophages without inducing noticeable adverse effects. Given the crucial role of macrophages in viral infections, MΦ-NPs present a promising approach to combating emerging viral threats.
Authors
- Yiyan Yu (ORCID: https://orcid.org/0000-0002-7136-654X)
- Daniela Silva‐Ayala (ORCID: https://orcid.org/0000-0001-8942-3461)
- Zhidong Zhou (ORCID: https://orcid.org/0000-0001-5251-4108)
- Weiwei Gao (ORCID: https://orcid.org/0000-0001-5196-4887)
- Anthony Griffiths (ORCID: https://orcid.org/0000-0001-5435-8364)
- Ronnie H. Fang (ORCID: https://orcid.org/0000-0001-6373-3189)
- Liangfang Zhang (ORCID: https://orcid.org/0000-0003-0637-0654)
- Yifei Peng (ORCID: https://orcid.org/0009-0008-7363-8685)
Institutions
- Boston University (US)
- University of California San Diego (US)
- University of Missouri (US)
Publication Details
- Journal
- Nano Letters
- Published
- 2024-11-13
- DOI
- https://doi.org/10.1021/acs.nanolett.4c04653
- Citations
- 2
- Primary Topic
- Nanoplatforms for cancer theranostics
- Type
- article
- Field-Weighted Citation Impact
- 0.37
Funders
- Defense Threat Reduction Agency