Tai Chau Y, Weber Renata V, Mackinnon Susan E, Tung Thomas H
Division of Plastics and Orthopedics, Kern Medical Center, CA, USA.
Neurol Res. 2010 Apr;32(3):332-6. doi: 10.1179/174313209X385635. Epub 2009 Jun 30.
In the nerve allograft model, costimulation blockade has permitted good regeneration but is still inferior to the nerve isograft. We hypothesize that a short course of multiple costimulatory pathway blockade will be more effective in inhibiting the redundancy of the immune response and improve nerve regeneration through the nerve allograft.
The murine sciatic nerve allograft model was used to reconstruct a 1 cm sciatic nerve gap. Treatment consisted of the inhibition of the CD40, CD28/B7 and ICOS pathways and was compared with only single or double costimulation blockade. Assessment methods included quantitative histomorphometry and ELISPOT assay to quantify the host immune response after 3 weeks post-operatively.
Triple costimulation blockade permitted regeneration through the nerve allograft that was equivalent to the nerve isograft. A short course of three doses was more effective than a single dose for all combinations tested. ELISPOT assay demonstrated minimal in vitro immune response with a short course of double or triple pathway-blocking agents.
Costimulation blockade, especially with the simultaneous inhibition of multiple pathways, remains a promising strategy to promote regeneration through the peripheral nerve allograft, and may be uniquely suited to the temporary immunosuppressive requirements of the peripheral nerve allograft.
在神经同种异体移植模型中,共刺激阻断已使神经实现良好再生,但仍逊于神经自体移植。我们假设,短期多次阻断共刺激通路在抑制免疫反应冗余及促进神经同种异体移植后的神经再生方面会更有效。
采用小鼠坐骨神经同种异体移植模型重建1厘米的坐骨神经缺损。治疗方法包括抑制CD40、CD28/B7和ICOS通路,并与仅单次或双次共刺激阻断进行比较。评估方法包括术后3周进行定量组织形态计量学和ELISPOT分析以量化宿主免疫反应。
三联共刺激阻断使神经同种异体移植后的神经再生情况与神经自体移植相当。对于所有测试的组合,三剂短期治疗比单剂更有效。ELISPOT分析表明,短期使用双通路或三通路阻断剂时,体外免疫反应极小。
共刺激阻断,尤其是同时抑制多条通路,仍是促进周围神经同种异体移植后神经再生的一种有前景的策略,且可能特别适合周围神经同种异体移植的临时免疫抑制需求。