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Requirement of dual stimulation by homologous recombinant IL-2 and recombinant IL-12 for the in vitro production of interferon gamma by canine peripheral blood mononuclear cells. | LitMetric

AI Article Synopsis

  • Very few studies focus on altering immune responses in dogs, so this research examined the effects of recombinant canine IL-2 and IL-12 fusion protein on dog blood cells.
  • Recombinant IL-2 was found to effectively stimulate the growth of canine blood cells, while the combination of IL-12 and IL-2 boosted the production of interferon gamma, an important immune signaling molecule.
  • The findings indicate that using both IL-2 and IL-12 together could enhance immune responses in dogs, which may have implications for veterinary treatments.

Article Abstract

Background: Very few studies have been carried out so far aiming at modulating cellular immune responses in dogs. In this study, we evaluated the ability of recombinant canine IL-2 (rcaIL-2) and IL-12, in the form of a single-chain fusion protein (rsccaIL-12), to stimulate peripheral blood mononuclear cells (PBMC) of healthy mongrel dogs.

Results: Recombinant canine IL-2 purified from Escherichia coli or present in the supernatant of COS-7 cells transfected with pcDNA3.1-caIL-2 (COS-7 caIL-2 supernatant) was able to induce proliferation of CTLL-2 cells, thus showing their functional activity. In addition, purified rcaIL-2 and COS-7 caIL-2 supernatant stimulated resting canine PBMC proliferation to a level higher than baseline level. Neither COS-7 sccaIL-12 supernatant nor COS-7 caIL-2 supernatant alone was able to induce significant production of interferon gamma by resting PBMC. However, COS-7 sccaIL-12 supernatant in combination with COS-7 caIL-2 supernatant induced production of IFN-γ by those cells.

Conclusions: The data shown herein suggest that the combination of canine recombinant IL-12 and IL-2 can be useful to promote cellular immune responses in dogs.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4109786PMC
http://dx.doi.org/10.1186/1756-0500-7-460DOI Listing

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