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Recombinant Ov-ASP-1, a Th1-Biased Protein Adjuvant Derived from the Helminth Onchocerca volvulus, Can Directly Bind and Activate Antigen-Presenting Cells
Author(s) -
Yuxian He,
Sophie Joanna Barker,
Angus Macdonald,
Yu Yu,
Long Cao,
Jingjing Li,
Ranjit S. Parhar,
Susanne Heck,
Susanne Hartmann,
Douglas T. Golenbock,
Shibo Jiang,
N A Libri,
Amanda Semper,
William Rosenberg,
Sara Lustigman
Publication year - 2009
Publication title -
the journal of immunology
Language(s) - English
Resource type - Journals
eISSN - 1550-6606
pISSN - 0022-1767
DOI - 10.4049/jimmunol.0800531
Subject(s) - onchocerca volvulus , adjuvant , recombinant dna , antigen , helminths , biology , immunology , onchocerciasis , genetics , gene
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.

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