A Dual‐Membrane Biomimetic Nanoplatform Enables Triple‐Modal Therapy Against SARS‐CoV‐2 Through Viral Decoy, Inflammation Neutralizing, and Intracellular RNAi

The persistent evolution of SARS-CoV-2 and the concomitant risk of life-threatening hyperinflammation, such as cytokine storm syndrome, underscore the urgent need for therapeutic strategies that simultaneously target viral replication and dysregulated host immunity. Herein, we describe a dual-membrane biomimetic nanoplatform, designated [A&T]MLN, comprising siRNA-loaded lipid nanoparticles with a hybrid membrane derived from ACE2-overexpressing HEK293T cells and THP-1 macrophages. This design integrates a high-density viral decoy based on ACE2 with the inherent immunomodulatory capacity of macrophage membranes. [A&T]MLN demonstrates broad-spectrum and potent neutralization of diverse SARS-CoV-2 variants by competitively blocking viral entry, while actively scavenging key inflammatory cytokines (including IL-6, IL-1β, and TNF-α) via membrane-displayed receptors. In a murine model of acute lung injury that recapitulates COVID-19 immunopathology, [A&T]MLN treatment significantly attenuated pulmonary inflammation and tissue damage. Additionally, the platform enabled efficient cytosolic delivery of siRNA, establishing a third modality for intracellular suppression of viral gene expression. Collectively, [A&T]MLN represents a complementary triple-modal therapy that simultaneously addresses viral entry, intracellular replication, and hyperinflammation (the core interconnected pathologies of severe COVID-19), offering a versatile and adaptive strategy against evolving SARS-CoV-2 variants and related inflammatory syndromes.

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Publication Details

Journal
Advanced Science
Published
2026-09-06
DOI
https://doi.org/10.1002/advs.77581
Primary Topic
interferon and immune responses
Type
article
Field-Weighted Citation Impact
0.00
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article

A Dual‐Membrane Biomimetic Nanoplatform Enables Triple‐Modal Therapy Against SARS‐CoV‐2 Through Viral Decoy, Inflammation Neutralizing, and Intracellular RNAi

Shengya Liu, Haihua Xiao, Junwei Che, Pinghui Wu et al.
Advanced Science
interferon and immune responses
article

A Dual‐Membrane Biomimetic Nanoplatform Enables Triple‐Modal Therapy Against SARS‐CoV‐2 Through Viral Decoy, Inflammation Neutralizing, and Intracellular RNAi

Shengya Liu, Haihua Xiao, Junwei Che, Pinghui Wu, Xiao Li, Cuiling Zhang, Wenjie Yang, Zhiping Li, Chao Shang, Te Zhao, Yanan Zhai, Junjie Ding, Yuhua Ran, Lin Li, Dan Liu, Bohan Zhang, Jing Gao, Hui Li, Chunsheng Gao, Yi Li
article en

Abstract

The persistent evolution of SARS-CoV-2 and the concomitant risk of life-threatening hyperinflammation, such as cytokine storm syndrome, underscore the urgent need for therapeutic strategies that simultaneously target viral replication and dysregulated host immunity. Herein, we describe a dual-membrane biomimetic nanoplatform, designated [A&T]MLN, comprising siRNA-loaded lipid nanoparticles with a hybrid membrane derived from ACE2-overexpressing HEK293T cells and THP-1 macrophages. This design integrates a high-density viral decoy based on ACE2 with the inherent immunomodulatory capacity of macrophage membranes. [A&T]MLN demonstrates broad-spectrum and potent neutralization of diverse SARS-CoV-2 variants by competitively blocking viral entry, while actively scavenging key inflammatory cytokines (including IL-6, IL-1β, and TNF-α) via membrane-displayed receptors. In a murine model of acute lung injury that recapitulates COVID-19 immunopathology, [A&T]MLN treatment significantly attenuated pulmonary inflammation and tissue damage. Additionally, the platform enabled efficient cytosolic delivery of siRNA, establishing a third modality for intracellular suppression of viral gene expression. Collectively, [A&T]MLN represents a complementary triple-modal therapy that simultaneously addresses viral entry, intracellular replication, and hyperinflammation (the core interconnected pathologies of severe COVID-19), offering a versatile and adaptive strategy against evolving SARS-CoV-2 variants and related inflammatory syndromes.

Advanced Science
Chinese Academy of Sciences (CN), Peking University (CN), Academy of Military Medical Sciences (CN), Shenzhen International Travel Health Care Center (CN), Beijing Biocytogen (China) (CN), State Key Laboratory of Cryptology (CN), Chinese Academy of Agricultural Sciences (CN), Peking University Third Hospital (CN), Institute of Chemistry (CN)
Openalex Percentile: Top 17%
interferon and immune responses
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