TP53 缺失通过上调 NF-κB-IFN-β-MHC-Ia 信号促进骨肉瘤对 NK 细胞的抵抗
TP53 Loss Elevates NF-κB-IFN-β-MHC-Ia Signaling to Promote NK Cell Resistance in Osteosarcoma.
CELL INTELLIGENCE · 肿瘤细胞治疗研究
肿瘤细胞治疗研究
英文原题:Safety assessment of equine allogeneic tenogenic primed mesenchymal stem cells in horses with naturally occurring tendon and ligament injuries.
Safety assessment of equine allogeneic tenogenic primed mesenchymal stem cells in horses with naturally occurring tendon and ligament injuries.
分数与星级只用于站内排序 —— 不代表疗效、安全性或个人适用性。
与先前接触过 tpMSCs 的马的 PBMCs 共孵育 tpMSCs 未引发细胞免疫反应,且 tpMSCs 能够对受刺激的 T 淋巴细胞进行免疫调节。病灶内注射 tpMSCs 未引起血液学和生化参数的异常变化。
间充质干细胞为马骨科损伤提供了一种有价值的治疗选择。
本研究的目的是评估对自然发生浅表指屈肌腱(SDFT)和悬韧带(SL)损伤的客户所有马匹,进行肌腱生成素预处理马异体外周血来源间充质干细胞(tpMSCs)病灶内治疗后的血液学、生化、免疫学和免疫调节参数。
在改良混合淋巴细胞反应中评估了tpMSCs的免疫原性和免疫调节能力,该反应包括来自14匹接受tpMSCs治疗后患有SDFT和SL损伤的马的外周血单核细胞(PBMCs)。在第二项研究中,18匹患有SDFT和SL损伤的马接受了tpMSCs病灶内注射(n = 9)或未接受治疗(n = 9)。
tpMSCs未引发细胞免疫反应(p < 0.001),并能在体外对受刺激的T淋巴细胞进行免疫调节(p < 0.001)。使用tpMSCs进行治疗未导致相关的血液学或生化异常。主要局限性:两项研究样本量均较小。第二项研究未进行统计分析。仅在一匹马治疗前分析了纤维蛋白原。
Mesenchymal stem cells provide a valuable treatment option in orthopedic injuries in horses.
The aim of this study was to evaluate the hematological, biochemical, immunological and immunomodulatory parameters following intralesional treatment with tenogenic primed equine allogeneic peripheral blood-derived mesenchymal stem cells (tpMSCs) in client-owned horses with naturally occurring superficial digital flexor tendon (SDFT) and suspensory ligament (SL) injuries.
The immunogenicity and immunomodulatory capacities of tpMSCs were assessed in a modified mixed lymphocyte reaction, including peripheral blood mononuclear cells (PBMCs) of 14 horses with SDFT and SL injuries after treatment with tpMSCs. In a second study, 18 horses with SDFT and SL injuries received either an intralesional injection with tpMSCs ( n = 9) or no treatment ( n = 9).
The tpMSCs did not provoke a cellular immune response ( p < 0.001) and were able to immunomodulate stimulated T lymphocytes ( p < 0.001) in vitro . Therapeutic use of tpMSCs did not result in relevant hematologic or biochemical abnormalities. MAIN LIMITATIONS: Both studies had a small sample size. No statistical analyses were performed in the second study. Fibrinogen was only analyzed in a single horse prior to treatment.
Co-incubation of tpMSCs and PBMCs of horses that have been previously exposed to tpMSCs did not elicit a cellular immune response and tpMSCs were able to immunomodulate stimulated T lymphocytes. Intralesional treatment with tpMSCs did not provoke abnormal changes in hematological and biochemical parameters.
在 PubMed 查看 → 出版商原文(DOI) 全文 PDF(PMC)· 可下载 治疗专题与资料阅读指南 资料来源与翻译说明 报告译文或资料问题 →
MEMBER ACCOUNT
登录成功会直接打开下一页。