Baylx, Inc., Irvine, CA, USA.
Sue and Bill Gross Stem Cell Research Center, University of California, Irvine, CA, USA.
Cell Transplant. 2020 Jan-Dec;29:963689720965896. doi: 10.1177/0963689720965896.
Rheumatoid arthritis (RA) is an inflammatory disease of the joints, which causes severe pain and excessive systemic circulation of harmful inflammatory cytokines. Current treatments are limited, with some patients not responding well, and some experiencing severe and detrimental side effects. Mesenchymal stem cells (MSC) are cell-based therapeutics being evaluated as potent immunomodulators in RA and may provide relief to patients not responding well to drug-based treatments. We evaluated the safety and efficacy of BX-U001 human umbilical cord tissue-derived mesenchymal stem cells (hUC-MSC) to treat RA, in support of a successful investigational new drug application. A collagen-induced arthritis (CIA) mouse model of RA was established in DBA/1 J mice. Mice from the treatment assessment group were given a tail vein infusion of hUC-MSC 24 days after primary RA induction, while control assessment (CA) group mice were given cell-free carrier solution. All animals were evaluated daily for RA symptoms via clinical scoring, blood was taken periodically for cytokine analysis, and mice were dissected at end point for histological analysis. A linear mixed model was used to compare the rate of change among groups. The clinical scores of TA group were significantly reduced compared with CA group ( < 0.01), indicating therapeutic effects. The histological scores of the joints in TA group were significantly lower than those in the CA group ( < 0.05), but had no significant difference compared with Healthy groups ( > 0.05). The concentration of (interleukin) IL-6 in TA group was significantly reduced by 80.0% ( < 0.0001) 2 days after treatment and by 93.4% at the experimental endpoint compared with levels prior to hUC-MSC injection. A single intravenous infusion of hUC-MSC (2 × 10 cells/mouse), to CIA-induced DBA/1 J mice, resulted in significant alleviation of RA symptoms and may provide significant therapeutic benefits in humans.
类风湿关节炎(RA)是一种关节炎症性疾病,可导致严重疼痛和有害炎症细胞因子在全身循环中过度增加。目前的治疗方法有限,一些患者反应不佳,有些患者则出现严重且有害的副作用。间充质干细胞(MSC)是一种基于细胞的治疗方法,被评估为 RA 中的有效免疫调节剂,可为对药物治疗反应不佳的患者提供缓解。我们评估了 BX-U001 人脐带组织来源间充质干细胞(hUC-MSC)治疗 RA 的安全性和疗效,以支持成功的新药研究申请。在 DBA/1 J 小鼠中建立了胶原诱导性关节炎(CIA)RA 小鼠模型。在原发性 RA 诱导后 24 天,治疗评估组的小鼠接受尾静脉输注 hUC-MSC,而对照评估(CA)组的小鼠接受无细胞载体溶液。所有动物每天通过临床评分评估 RA 症状,定期采血进行细胞因子分析,并在终点进行解剖以进行组织学分析。使用线性混合模型比较组间的变化率。与 CA 组相比,TA 组的临床评分明显降低(<0.01),表明具有治疗效果。TA 组关节的组织学评分明显低于 CA 组(<0.05),但与健康组相比无显著差异(>0.05)。TA 组的(白细胞介素)IL-6 浓度在治疗后 2 天降低了 80.0%(<0.0001),在实验终点时与 hUC-MSC 注射前相比降低了 93.4%。单次静脉输注(2×10 个细胞/只)hUC-MSC 可显著缓解 CIA 诱导的 DBA/1 J 小鼠的 RA 症状,并可能为人类提供显著的治疗益处。