Abstract
We previously reported that rOv-ASP-1, a recombinant Onchocerca volvulus activation associated protein-1, was a potent adjuvant for recombinant protein or synthetic peptide-based Ags. In this study, we further evaluated the adjuvanticity of rOv-ASP-1 and explored its mechanism of action. Consistently, recombinant full-length spike protein of SARS-CoV or its receptor-binding domain in the presence of rOv-ASP-1 could effectively induce a mixed but Th1-skewed immune response in immunized mice. It appears that rOv-ASP-1 primarily bound to the APCs among human PBMCs and triggered Th1-biased proinflammatory cytokine production probably via the activation of monocyte-derived dendritic cells and the TLR, TLR2, and TLR4, thus suggesting that rOv-ASP-1 is a novel potent innate adjuvant.
MeSH terms
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Adjuvants, Immunologic*
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Animals
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Antigen Presentation / immunology
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Antigen-Presenting Cells / immunology*
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Antigens, Helminth / immunology*
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Cytokines / biosynthesis
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Enzyme-Linked Immunosorbent Assay
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Flow Cytometry
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Helminth Proteins / immunology*
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Humans
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Lymphocyte Activation / immunology*
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Membrane Glycoproteins / immunology
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Mice
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Recombinant Proteins / immunology*
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Spike Glycoprotein, Coronavirus
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Th1 Cells / immunology*
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Th2 Cells / immunology
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Toll-Like Receptor 2 / immunology
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Toll-Like Receptor 4 / immunology
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Viral Envelope Proteins / immunology
Substances
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Adjuvants, Immunologic
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Antigens, Helminth
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Cytokines
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Helminth Proteins
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Membrane Glycoproteins
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Ov-ASP-1 protein, Onchocerca volvulus
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Recombinant Proteins
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Spike Glycoprotein, Coronavirus
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Toll-Like Receptor 2
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Toll-Like Receptor 4
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Viral Envelope Proteins