Nixon A J, Rickey E, Butler T J, Scimeca M S, Moran N, Matthews G L
Comparative Orthopedics Laboratory, Department of Clinical Sciences, College of Veterinary Medicine, Cornell University, Ithaca, NY 14853, USA.
Comparative Orthopedics Laboratory, Department of Clinical Sciences, College of Veterinary Medicine, Cornell University, Ithaca, NY 14853, USA.
Osteoarthritis Cartilage. 2015 Apr;23(4):648-60. doi: 10.1016/j.joca.2014.12.021. Epub 2015 Jan 7.
Autologous chondrocyte implantation (ACI) has improved outcome in long-term studies of joint repair in man. However, ACI requires sutured periosteal flaps to secure the cells, which precludes minimally-invasive implantation, and introduces complications with arthrofibrosis and graft hypertrophy. This study evaluated ACI on a collagen type I/III scaffold (matrix-induced autologous chondrocyte implantation; MACI(®)) in critical sized defects in the equine model.
Chondrocytes were isolated from horses, expanded and seeded onto a collagen I/III membrane (ACI-Maix™) and implanted into one of two 15-mm defects in the femoral trochlear ridge of six horses. Control defects remained empty as ungrafted debrided defects. The animals were examined daily, scored by second look arthroscopy at 12 weeks, and necropsy examination 6 months after implantation. Reaction to the implant was determined by lameness, and synovial fluid constituents and synovial membrane histology. Cartilage healing was assessed by arthroscopic scores, gross assessment, repair tissue histology and immunohistochemistry, cartilage glycosaminoglycan (GAG) and DNA assay, and mechanical testing.
MACI(®) implanted defects had improved arthroscopic second-look, gross healing, and composite histologic scores, compared to spontaneously healing empty defects. Cartilage GAG and DNA content in the defects repaired by MACI implant were significantly improved compared to controls. Mechanical properties were improved but remained inferior to normal cartilage. There was minimal evidence of reaction to the implant in the synovial fluid, synovial membrane, subchondral bone, or cartilage.
The MACI(®) implant appeared to improve cartilage healing in a critical sized defect in the equine model evaluated over 6 months.
在人体关节修复的长期研究中,自体软骨细胞植入(ACI)改善了治疗效果。然而,ACI需要缝合骨膜瓣来固定细胞,这排除了微创植入的可能性,并引发关节纤维化和移植物肥大等并发症。本研究在马模型的临界尺寸缺损中评估了I/III型胶原蛋白支架上的ACI(基质诱导自体软骨细胞植入;MACI(®))。
从马身上分离软骨细胞,进行扩增并接种到I/III型胶原膜(ACI-Maix™)上,然后植入6匹马股骨滑车嵴上两个15毫米缺损中的一个。对照缺损作为未移植的清创缺损保持空置。每天对动物进行检查,在12周时通过二次关节镜检查评分,并在植入后6个月进行尸检。通过跛行、滑液成分和滑膜组织学来确定对植入物的反应。通过关节镜评分、大体评估、修复组织组织学和免疫组织化学、软骨糖胺聚糖(GAG)和DNA检测以及力学测试来评估软骨愈合情况。
与自发愈合的空置缺损相比,植入MACI(®)的缺损在关节镜二次检查、大体愈合和综合组织学评分方面有所改善。与对照组相比,MACI植入修复的缺损中的软骨GAG和DNA含量显著提高。力学性能有所改善,但仍低于正常软骨。在滑液、滑膜、软骨下骨或软骨中对植入物反应的证据极少。
在超过6个月的评估期内,MACI(®)植入物似乎改善了马模型临界尺寸缺损中的软骨愈合。