Mierisch Cay M, Cohen Steven B, Jordan Louis C, Robertson Peter G, Balian Gary, Diduch David R
Orthopaedic Research Laboratory, Department of Orthopaedic Surgery, University of Virginia School of Medicine, Charlottesville, Virginia, USA.
Arthroscopy. 2002 Oct;18(8):892-900. doi: 10.1053/jars.2002.36117.
Articular cartilage has only limited capability for intrinsic repair. The use of growth factors has been suggested to improve the repair of cartilage after injury. Reliable delivery systems for these agents are needed. In this study we tested calcium alginate for the delivery of TGF-beta in the treatment of osteochondral defects in the rabbit knee.
Randomized trial animal study and basic science study.
In vitro, to establish the kinetics of TGF-beta release from the alginate, 125I- labeled TGF-beta was suspended in 1.2% sodium alginate at concentrations of 1 microg/mL and 10 microg/mL. Beads were formed from 50 microL aliquots and placed into standard culture medium by immersion in calcium chloride solution and incubated at 37 degrees C. A gamma counter was used to measure the amount of TGF-beta that was released into the medium at various time points. In vivo, osteochondral defects were created in the trochlear grooves of 32 New Zealand White rabbits. Defects were treated with plain alginate or with alginate containing TGF-beta at 20 ng/mL or 2,000 ng/mL. Untreated defects served as a control. Animals were killed after 6 and 12 weeks. Knee joints were evaluated grossly with a 12-point grading scale. Histologic sections of the repair tissue were stained with Safranin O and evaluated using a 24-point grading scale by 2 independent blinded observers. Mean scores and standard deviations were calculated. P values were determined using the Student t test.
The TGF-beta was released at a surprisingly slow but steady rate. Release rates extrapolated from the gamma counter measurements were 0.25% per hour and 0.33% per hour, for the 1 microg/mL and 10 microg/mL beads, respectively. Gross analysis scores at 6 and 12 weeks resulted in higher scores for both TGF-beta groups without reaching statistical significance. The lower TGF-beta concentration reached the highest scores, whereas the higher concentration (2,000 ng/mL) resulted in increased osteophyte formation. Histologic analysis at 6 weeks resulted in average scores ranging from 14.5 for empty defects and 18.1 for alginate-treated defects, to 20.0 and 20.3 for the 2,000 ng/mL and 20 ng/mL TGF-beta groups, respectively (P <.05). At 12 weeks, histologic scores ranged from 14.9 for empty and 14.5 for alginate to 20.1 and 20.5 for the 2,000 ng/mL and 20 ng/mL TGF-beta groups, respectively (P <.05). These results indicate a significant improvement of the quality of the repair tissue at 6 and 12 weeks with TFG-beta treatment, especially at the lower concentration.
The use of alginate allows the controlled delivery of TGF-beta selectively to the site of injury, potentially avoiding systemic side effects. Furthermore, treatment with TGF-beta appears to improve the repair of articular cartilage defects. Longer-term studies are needed to assess whether the benefits of the TGF-beta treatment can be sustained.
关节软骨自身修复能力有限。有人提出使用生长因子来促进损伤后软骨的修复。需要可靠的这些因子递送系统。在本研究中,我们测试了海藻酸钙用于在兔膝关节治疗骨软骨缺损时递送转化生长因子-β(TGF-β)。
随机试验动物研究和基础科学研究。
在体外,为确定TGF-β从海藻酸盐中的释放动力学,将125I标记的TGF-β以1微克/毫升和10微克/毫升的浓度悬浮于1.2%的海藻酸钠中。从50微升等分试样形成珠子,通过浸入氯化钙溶液放入标准培养基中,并在37℃孵育。使用γ计数器测量在不同时间点释放到培养基中的TGF-β量。在体内,在32只新西兰白兔的滑车沟中制造骨软骨缺损。缺损用普通海藻酸盐或含20纳克/毫升或2000纳克/毫升TGF-β的海藻酸盐治疗。未治疗的缺损作为对照。6周和12周后处死动物。用12分制评分系统对膝关节进行大体评估。修复组织的组织学切片用番红O染色,并由2名独立的盲法观察者使用24分制评分系统进行评估。计算平均分和标准差。使用学生t检验确定P值。
TGF-β以惊人的缓慢但稳定的速率释放。从γ计数器测量推断的释放速率,对于1微克/毫升和10微克/毫升的珠子,分别为每小时0.25%和每小时0.33%。6周和12周时的大体分析评分,两个TGF-β组的评分更高,但未达到统计学意义。较低的TGF-β浓度达到最高分,而较高浓度(2000纳克/毫升)导致骨赘形成增加。6周时的组织学分析,平均分范围从空白缺损的14.5、海藻酸盐治疗缺损的18.1,到2000纳克/毫升和20纳克/毫升TGF-β组的20.0和20.3(P<.05)。12周时,组织学评分范围从空白的14.9和海藻酸盐的14.5,到2000纳克/毫升和20纳克/毫升TGF-β组的20.1和20.5(P<.05)。这些结果表明,用TGF-β治疗在6周和12周时修复组织质量有显著改善,尤其是在较低浓度时。
使用海藻酸盐可将TGF-β选择性地控制递送至损伤部位,可能避免全身副作用。此外,TGF-β治疗似乎可改善关节软骨缺损的修复。需要进行长期研究以评估TGF-β治疗的益处是否可持续。