Pezzanite Lynn M, Timkovich Ariel E, Sikes Katie J, Chow Lyndah, Hendrickson Dean A, Becker Jordyn R, Webster Aaron, Santangelo Kelly S, Dow Steven
Department of Clinical Sciences, College of Veterinary Medicine and Biomedical Sciences, Colorado State University, Fort Collins, CO, USA.
Department of Microbiology, Immunology and Pathology, College of Veterinary Medicine and Biomedical Sciences, Colorado State University, Fort Collins, CO, USA.
Ann Transl Med. 2023 Jun 30;11(9):311. doi: 10.21037/atm-22-4256. Epub 2023 May 25.
Despite the high prevalence of osteoarthritis (OA), there remains a need for additional therapeutic options. Cellular therapies with minimally manipulated cells such as bone marrow aspirate concentrates (BMAC) are increasingly popular in the U.S. but clear-cut evidence of efficacy has not been established. In theory, BMAC injections provide a source of stromal cells to stimulate healing in OA and ligamentous injuries; however, BMAC injections are also often associated with inflammation, short-term pain, and mobility impairment. Given that blood is known to trigger inflammation in joints, we hypothesized that removing erythrocytes [red blood cells (RBCs)] from BMAC preparations prior to intra-articular injection would improve efficacy for OA treatment.
To test this hypothesis, BMAC was collected from the bone marrow of mice. Three treatment groups were pursued: (I) untreated; (II) BMAC; or (III) BMAC depleted of RBCs by lysis. Product was injected into the femorotibial joint of mice 7 days after OA had been induced by destabilization of the medial meniscus (DMM). To assess the impact of treatment on joint function, individual cage monitoring (ANY-maze) and Digigait treadmill-based analyses were performed over 4 weeks. At study completion, joint histopathology was assessed and immune transcriptomes within joint tissues were compared using a species-specific NanoString panel.
Significant improvements in activity, gait parameters, and histology scores were seen in animals receiving RBC-depleted BMAC compared to untreated mice; animals treated with non-depleted BMAC did not demonstrate this same extent of consistent significant improvement. Transcriptomic analysis of joint tissues revealed significant upregulation of key anti-inflammatory genes, including interleukin-1 receptor antagonist (IRAP), in mice treated with RBC-depleted BMAC compared to animals treated with non-RBC depleted BMAC.
These findings indicate that RBC depletion in BMAC prior to intra-articular injection improves treatment efficacy and reduces joint inflammation compared to BMAC.
尽管骨关节炎(OA)的患病率很高,但仍需要更多的治疗选择。在美国,使用如骨髓抽吸浓缩物(BMAC)等经过最少操作的细胞进行细胞治疗越来越普遍,但尚未确立明确的疗效证据。理论上,BMAC注射可提供基质细胞来源,以促进OA和韧带损伤的愈合;然而,BMAC注射也常与炎症、短期疼痛和活动能力受损相关。鉴于已知血液会引发关节炎症,我们推测在关节内注射前从BMAC制剂中去除红细胞(RBC)可提高OA治疗的疗效。
为验证这一假设,从小鼠骨髓中收集BMAC。设立三个治疗组:(I)未治疗组;(II)BMAC组;或(III)通过裂解去除RBC的BMAC组。在通过内侧半月板不稳定(DMM)诱导OA 7天后,将产物注射到小鼠的股胫关节中。为评估治疗对关节功能的影响,在4周内进行个体笼内监测(ANY-maze)和基于Digigait跑步机的分析。研究结束时,评估关节组织病理学,并使用物种特异性NanoString面板比较关节组织内的免疫转录组。
与未治疗的小鼠相比,接受去除RBC的BMAC治疗的动物在活动、步态参数和组织学评分方面有显著改善;接受未去除RBC的BMAC治疗的动物未表现出同样程度的持续显著改善。与接受未去除RBC的BMAC治疗的动物相比,对接受去除RBC的BMAC治疗的小鼠关节组织进行转录组分析发现关键抗炎基因(包括白细胞介素-1受体拮抗剂(IRAP))显著上调。
这些发现表明,与BMAC相比,关节内注射前对BMAC进行RBC去除可提高治疗效果并减轻关节炎症。