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Peer-reviewed veterinary case report

Uterine stem cell treatment for itching and skin issues in dogs

By Black, Linda et al.·Published in Frontiers in veterinary science·2022·Gallant Therapeutics, United States·View original on PubMed

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Original publication title: The effect of uterine-derived mesenchymal stromal cells for the treatment of canine atopic dermatitis: A pilot study.

Species:
dog

Plain-English summary

A group of seven dogs with atopic dermatitis (a common allergic skin condition) received two intravenous treatments of uterine-derived stem cells to see if it would help reduce their itching and skin lesions. The treatments were well tolerated, and by Day 60, most of the dogs showed significant improvement in their symptoms, with some experiencing a reduction in itching scores by 4-5 points. The benefits lasted for several months, suggesting that this treatment could be a promising option for managing atopic dermatitis in dogs.

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Abstract

Canine atopic dermatitis (cAD) is a common allergic skin condition among dogs that may respond to treatment with mesenchymal stromal cells (MSCs). The aim of this pilot study was to evaluate the safety and efficacy of allogeneic uterine tissue-derived MSCs (UMSCs) for the reduction and control of clinical signs associated with cAD. At two sites, seven client-owned dogs with cAD received two doses of approximately 3.6 x 10UMSCs given intravenously over 30 min, on Day 0 and Day 14, with monthly clinical follow-up until Day 90 and optional owner phone interview on Day 180. Primary outcomes were pruritus and skin lesions. Pruritus was measured by the owner-assessed Pruritus Visual Analog Scale (PVAS), with treatment success defined as a 2-point reduction in PVAS score at any timepoint after treatment. Skin lesions were evaluated by two veterinarians according to the Canine Atopic Dermatitis Extent and Severity Index (CADESI-4). The secondary outcome was safety, which was evaluatedphysical exam and hematology, including complete blood count (CBC), serum chemistry, and urinalysis (UA). Treatment was generally well tolerated and associated with a significant reduction in PVAS on Day 30 that was maintained through Day 180. On Day 60, five dogs (71%) achieved treatment success (at least 2-point reduction in PVAS), and three dogs (43%) had a PVAS improvement of 4-5 points. Mean CADESI-4 score was significantly improved on Day 14, Day 30, Day 60, and Day 90, with the lowest mean score observed on Day 60. Three dogs exhibited mild and transient adverse events. These findings suggest that IV-administered allogeneic UMSCs reduce and control clinical signs of cAD, with a durable benefit lasting 3-6 months.

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Original publication on PubMed: https://pubmed.ncbi.nlm.nih.gov/36213399/