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. 2020 Jul 29:10.2217/nnm-2020-0247. doi: 10.2217/nnm-2020-0247

Table 2. Nanoparticles-based vaccination against coronaviruses.

  Platform Antigenic component Virus Notes Ref.
Self-assembled NPs Spike protein NPs Spike protein SARS-CoV, MERS-CoV Induce high level of neutralizing antibodies
Adjuvants (Alum, Matrix) improved safety and immunogenicity
[1,7]
Spike protein-displaying VLPs   MERS-CoV Spike protein attaches DPP4 receptors, stimulating immune system [126]
RBD-displaying VLPs Gene of RBD of spike protein MERS-CoV Induced RBD-specific immune responses
Antisera protected host cells from CoV infection
[127]
Chaperna-based NPs   MERS-CoV Induced mice immunization via interfering with binding of RBD to DPP4 receptors [128]
Polypeptide NPs HRC1 epitope of spike protein SARS-CoV Specific, work against SARS-CoV and any enveloped virus [132]
AuNPs S-AuNPs Spike protein of avian CoV Avian CoV Significant improvement in vaccination potency [133]
S-AuNPs Spike protein SARS-CoV Induced strong IgG responses
Lung eosinophilic immunopathology
[6]

CoV: Coronavirus; MERS-CoV: Middle East respiratory syndrome coronavirus; NP: Nanoparticle; RBD: Receptor-binding domains; S-AuNP: Spike proteins-functionalized gold NP; SARS-CoV: Severe acute respiratory syndrome coronavirus; VLP: Virus-like particle.