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首页> 外文期刊>Veterinary and Comparative Orthopaedics and Traumatology >Inflammatory effects of autologous, genetically modified autologous, allogeneic, and xenogeneic mesenchymal stem cells after intra-articular injection in horses.
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Inflammatory effects of autologous, genetically modified autologous, allogeneic, and xenogeneic mesenchymal stem cells after intra-articular injection in horses.

机译:在马关节内注射后自体,基因修饰的自体,同种异体和异种间充质干细胞的炎症作用。

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Objectives: To compare the clinical and inflammatory joint responses to intra-articular injection of bone marrow-derived mesenchymal stem cells (MSC) including autologous, genetically modified autologous, allogeneic, or xenogeneic cells in horses. Methods: Six five-year-old Thoroughbred mares had one fetlock joint injected with Gey's balanced salt solution as the vehicle control. Each fetlock joint of each horse was subsequently injected with 15 million MSC from the described MSC groups, and were assessed for 28 days for clinical and inflammatory parameters representing synovitis, joint swelling, and pain. Results: There were not any significant differences between autologous and genetically modified autologous MSC for synovial fluid total nucleated cell count, total protein, interleukin (IL)-6, IL-10, fetlock circumference, oedema score, pain-free range-of-motion, and soluble gene products that were detected for at least two days. Allogeneic and xenogeneic MSC produced a greater increase in peak of inflammation at 24 hours than either autologous MSC group. Clinical significance: Genetically engineered MSC can act as vehicles to deliver gene products to the joint; further investigation into the therapeutic potential of this cell therapy is warranted. Intra-articular MSC injection resulted in a moderate acute inflammatory joint response that was greater for allogeneic and xenogeneic MSC than autologous MSC. Clinical management of this response may minimize this effect.
机译:目的:比较关节内注射骨髓源性间充质干细胞(MSC)的临床和炎性关节反应,其中包括自体,基因修饰的自体,同种或异种细胞。方法:六只五岁的纯种母马用一根吉特的平衡盐溶液注射了一个羊群关节作为媒介物对照。随后向每匹马的每个节肢关节注射来自所述MSC组的1500万个MSC,并评估28天的临床和炎症参数,这些参数代表滑膜炎,关节肿胀和疼痛。结果:自体和基因改造的自体MSC在滑液总有核细胞数,总蛋白,白介素(IL)-6,IL-10,血脂周,水肿评分,无痛范围内无明显差异。至少检测到两天的运动和可溶性基因产物。同种和异种MSC在24小时的炎症峰值均比任何一个自体MSC组都大。临床意义:基因工程的MSC可以作为将基因产物传递到关节的媒介。有必要进一步研究这种细胞疗法的治疗潜力。关节腔内MSC注射导致中度急性炎症关节反应,同种和异种MSC均比自体MSC大。这种反应的临床管理可能会最小化这种影响。

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