Intravenous Allogeneic Mesenchymal Stem Cell Therapy for Canine Immune-Mediated Hemolytic Anemia: A Retrospective Clinical Evaluation.

IF 2
Steven D Garner, Emily D Laughrun
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Abstract

This study evaluates the clinical efficacy and safety of intravenous allogeneic mesenchymal stem cell (MSC) therapy as an adjunct to standard immunosuppressive treatment in dogs diagnosed with primary immune-mediated hemolytic anemia (IMHA), particularly in cases with inadequate response to conventional immunosuppressive protocols. A total of 157 client-owned dogs with IMHA received MSC therapy at Safari Veterinary Care Center or collaborating clinics. A core cohort of 43 dogs met strict inclusion criteria: confirmed primary IMHA, no significant comorbidities, and receipt of at least two MSC treatments. A retrospective analysis was performed on medical records of treated dogs. Packed cell volume (PCV) trends were used to assess treatment response, with success defined as sustained improvement to ≥30% PCV following MSC therapy. Safety was assessed by reviewing for adverse reactions postinfusion. In the core cohort, 76% (33/43) of dogs achieved successful hematological recovery. Across the broader cohort, clinical improvement was also observed, particularly in dogs with poor initial response to standard therapy. No serious adverse events were recorded following MSC infusion. Allogeneic MSC therapy appears to be a well-tolerated and potentially effective adjunctive treatment for canine IMHA, particularly in refractory cases. These findings support further investigation in controlled clinical trials.

静脉注射同种异体间充质干细胞治疗犬免疫介导的溶血性贫血:回顾性临床评价。
本研究评估了静脉注射同种异体间充质干细胞(MSC)治疗作为标准免疫抑制治疗的辅助疗法对原发性免疫介导溶血性贫血(IMHA)犬的临床疗效和安全性,特别是在对常规免疫抑制方案反应不足的情况下。共有157只患有IMHA的客户拥有的狗在Safari兽医护理中心或合作诊所接受了MSC治疗。43只狗的核心队列符合严格的纳入标准:确认原发性IMHA,无显著合并症,接受至少两次MSC治疗。对治疗犬的医疗记录进行回顾性分析。填充细胞体积(PCV)趋势用于评估治疗反应,成功定义为MSC治疗后PCV持续改善至≥30%。通过回顾输液后的不良反应来评估安全性。在核心队列中,76%(33/43)的狗获得了成功的血液恢复。在更广泛的队列中,也观察到临床改善,特别是对标准治疗最初反应不佳的狗。MSC输注后无严重不良事件记录。同种异体间充质干细胞治疗似乎是一种耐受性良好且潜在有效的辅助治疗犬IMHA,特别是在难治性病例中。这些发现支持在对照临床试验中进一步调查。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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