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Peer-reviewed veterinary case report

Effect of recombinant canine interferon-γ on granulocyte-macrophage colony-stimulating factor, transforming growth factor-β and CC chemokine ligand 17 mRNA transcription in a canine keratinocyte cell line (CPEK).

Journal:
Veterinary dermatology
Year:
2011
Authors:
Shibata, Sanae et al.
Affiliation:
The United Graduate School of Veterinary Sciences · Japan
Species:
dog

Abstract

Recombinant canine interferon-&#x3b3; (rCaIFN-&#x3b3;) produced by a baculovirus expression system has therapeutic efficacy against atopic dermatitis in dogs. Although the mechanism of action of rCaIFN-&#x3b3; is not completely understood, rCaIFN-&#x3b3; is thought to downregulate the activity of interleukin-4- and interleukin-5-producing T helper 2 cells. However, rCaIFN-&#x3b3; may also act directly on canine keratinocytes by inhibiting the release of inflammatory mediators. In this study, we investigated the effects of rCaIFN-&#x3b3; on cytokine and chemokine mRNA transcription in a canine keratinocyte cell line, CPEK. It was found that granulocyte-macrophage colony-stimulating factor (GM-CSF) mRNA transcription was significantly inhibited after treatment with rCaIFN-&#x3b3; (P<0.001), whereas transforming growth factor-&#x3b2; and CC chemokine ligand 17 mRNA levels were unchanged. This study suggests that rCaIFN-&#x3b3; may suppress GM-CSF production from canine keratinocytes, although further studies are required to confirm this.

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Original publication: https://pubmed.ncbi.nlm.nih.gov/20860556/