Amantadine-assembled nanostimulator enhances dimeric RBD antigen-elicited cross-neutralization against SARS-CoV-2 strains
Nano Today, ISSN: 1748-0132, Vol: 43, Page: 101393
2022
- 3Citations
- 14Captures
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Metrics Details
- Citations3
- Citation Indexes3
- Captures14
- Readers14
- 14
Article Description
There is an urgent need to develop new vaccination strategies to elevate the cross-neutralization against different SARS-CoV-2 strains. In this study, we construct the spherical amantadine-assembled nanostimulator (AAS). Amantadine as immunostimulating molecules are displayed on the outermost layer of AAS. Molecular mechanism analysis reveals that AAS can activate RIG-I-like receptor (RLR) signaling pathway to increase the expression of type I interferons in vivo. AAS-mediated activation of RLR signaling pathway further promotes the maturation and proliferation of dendritic cells (DCs) and T helper cells (Ths), finally activating B cells to produce potent antibody responses. In performance evaluation experiments, the mixture of AAS and dimeric RBD significantly enhances RBD-specific humoral responses (4-fold IgG, 3.5-fold IgG2a, 3.3-fold IgG2b, 3.8-fold IgG3 and 1.3-fold IgM), in comparison to aluminum adjuvant-assistant dimeric RBD. Importantly, AAS dramatically elevates dimeric RBD-elicited cross-neutralization against different SARS-CoV-2 strains such as Wuhan-Hu-1 (9-fold), B.1.1.7 (UK variant, 15-fold), B.1.351 (South African variant, 4-fold) and B.1.617.2 (India variant, 7-fold). Our study verifies the mechanism of AAS in activating RLR signaling pathway in host immune system and highlights the power of AAS in improving antigen-elicited cross-neutralization against different SARS-CoV-2 strains.
Bibliographic Details
http://www.sciencedirect.com/science/article/pii/S1748013222000202; http://dx.doi.org/10.1016/j.nantod.2022.101393; http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=85122673319&origin=inward; http://www.ncbi.nlm.nih.gov/pubmed/35035515; https://linkinghub.elsevier.com/retrieve/pii/S1748013222000202; https://dx.doi.org/10.1016/j.nantod.2022.101393
Elsevier BV
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