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.

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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

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article

Cellular Nanoparticles Treat Coronavirus Infection in Vivo

Yiyan Yu, Daniela Silva‐Ayala, Zhidong Zhou, Weiwei Gao et al.
2 citations
Nano Letters
Nanoplatforms for cancer theranostics
0.37
article

Cellular Nanoparticles Treat Coronavirus Infection in Vivo

Yiyan Yu, Daniela Silva‐Ayala, Zhidong Zhou, Weiwei Gao, Anthony Griffiths, Ronnie H. Fang, Liangfang Zhang, Yifei Peng
article en
2 citations

Abstract

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.

Nano LettersVol. 24(47)
Boston University (US), University of California San Diego (US), University of Missouri (US)
Defense Threat Reduction Agency
Good health and well-being
Openalex Percentile: Top 42%
Nanoplatforms for cancer theranostics
0.37
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Cellular Nanoparticles Treat Coronavirus Infection <i>in Vivo</i> — Yiyan Yu, Daniela Silva‐Ayala, et al. · Nano Letters (2024) | TGRS Research Map | TGRS