Skip to main navigation Skip to search Skip to main content

Recombinant Ov-ASP-1, a Th1-biased protein adjuvant derived from the helminth Onchocerca volvulus, can directly bind and activate antigen-presenting cells

  • Yuxian He*
  • , Sophie J. Barker
  • , Angus J. MacDonald
  • , Yu Yu
  • , Long Cao
  • , Jingjing Li
  • , Ranjit Parhar
  • , Susanne Heck
  • , Susanne Hartmann
  • , Douglas T. Golenbock
  • , Shibo Jiang
  • , Nathan A. Libri
  • , Amanda E. Semper
  • , William M. Rosenberg
  • , Sara Lustigman
  • *Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

37 Citations (Scopus)

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.

Original languageEnglish
Pages (from-to)4005-4016
Number of pages12
JournalJournal of Immunology
Volume182
Issue number7
DOIs
Publication statusPublished - 1 Apr 2009
Externally publishedYes

Fingerprint

Dive into the research topics of 'Recombinant Ov-ASP-1, a Th1-biased protein adjuvant derived from the helminth Onchocerca volvulus, can directly bind and activate antigen-presenting cells'. Together they form a unique fingerprint.

Cite this