AI Article Synopsis

  • A pharmacodynamic assay was developed to monitor ciclosporin treatments in dogs by measuring cytokine transcription inhibition after blood stimulation with PMA/I and LPS.
  • The study evaluated the effects of various immunosuppressive drugs (azathioprine, ciclosporin, mycophenolate, leflunomide, and prednisone) on cytokine production in healthy dogs after a week of treatment.
  • Results showed that ciclosporin and prednisone significantly reduced specific cytokines (IL-10, IFNγ, TNFα) after stimulation, while other drugs did not have notable effects; further research is needed for clinical applications.

Article Abstract

A pharmacodynamic assay has been previously developed to monitor ciclosporin treatment in dogs by assessing inhibition of cytokine transcription after whole blood stimulation with 12-myristate 13-1 acetate and ionomycin (PMA/I). In this study, whole blood stimulation with either PMA/I or lipopolysaccharide (LPS) was used to assess the effect of multiple drugs (azathioprine, ciclosporin, mycophenolate, leflunomide and prednisone) after a 7-day treatment course on production of cytokines measured with a multiplex assay in healthy dogs (n = 4 for each treatment). Interleukin-10 (IL-10), interferon gamma (IFNγ) and tumour necrosis factor alpha (TNFα) were significantly activated by PMA/I stimulation and IL-6, IL-10 and TNFα by LPS stimulation, in the absence of immunosuppressive drugs. After ciclosporin treatment, IL-10, IFNγ and TNFα production was significantly reduced after stimulation with PMA/I compared to pre-treatment. After prednisone treatment, TNFα production was significantly reduced after stimulation with PMA/I or LPS compared to pre-treatment. No significant change was observed after treatment with azathioprine, leflunomide or mycophenolate. This methodology may be useful to monitor dogs not only treated with ciclosporin, but also with prednisone or a combination of both. Further studies are needed to assess the use of this assay in a clinical setting.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6498811PMC
http://dx.doi.org/10.1002/vms3.143DOI Listing

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