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Peer-reviewed veterinary case report

Stem cells from dog amniotic membrane help treat atopic dermatitis

By Kim, Min Soo et al.·Published in Veterinary research communications·2023·Research Institute for Veterinary Science, South Korea·View original on PubMed

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Original publication title: Canine amniotic membrane-derived mesenchymal stem cells ameliorate atopic dermatitis through regeneration and immunomodulation.

Species:
dog

Plain-English summary

A study found that mesenchymal stem cells derived from canine amniotic membranes can help treat atopic dermatitis (a skin allergy) in dogs. These stem cells were shown to reduce skin inflammation and improve healing more effectively than a common medication called oclacitinib, which can cause weight loss as a side effect. The stem cells not only helped with skin symptoms but also promoted overall recovery without negative effects. This suggests that using these stem cells could be a promising and safer option for dogs suffering from atopic dermatitis.

People also search for: dog skin allergy treatment · atopic dermatitis in dogs · oclacitinib side effects · canine stem cell therapy · dog itching relief

Abstract

Mesenchymal stem cells (MSCs) are a promising tool for treating immune disorders. However, the immunomodulatory effects of canine MSCs compared with other commercialized biologics for treating immune disorders have not been well studied. In this study we investigated the characteristics and immunomodulatory effects of canine amnion membrane (cAM)-MSCs. We examined gene expression of immune modulation and T lymphocytes from activated canine peripheral blood mononuclear cell (PBMC) proliferation. As a result, we confirmed that cAM-MSCs upregulated immune modulation genes (TGF-β1, IDO1 and PTGES2) and suppressed the proliferation capacity of T cells. Moreover, we confirmed the therapeutic effect of cAM-MSCs compared with oclacitinib (OCL), the most commonly used Janus kinase (JAK) inhibitor, as a treatment for canine atopic dermatitis (AD) using a mouse AD model. As a result, we confirmed that cAM-MSCs with PBS treatment groups (passage 4, 6 and 8) compared with PBS only (PBS) though scores of dermatologic signs, tissue pathologic changes and inflammatory cytokines were significantly reduced. In particular, cAM-MSCs were more effective than OCL in the recovery of wound dysfunction, regulation of mast cell activity and expression level of immune modulation protein. Interestingly, subcutaneous injection of cAM-MSCs induced weight recovery, but oral administration of oclacitinib induced weight loss as a side effect. In conclusion, this study suggests that cAM-MSCs can be developed as a safe canine treatment for atopic dermatitis without side effects through effective regeneration and immunomodulation.

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Original publication on PubMed: https://pubmed.ncbi.nlm.nih.gov/37421548/