Willison Hugh J, Halstead Susan K, Beveridge Erin, Zitman Femke M P, Greenshields Kay N, Morgan B Paul, Plomp Jaap J
Division of Clinical Neurosciences, Glasgow Biomedical Research Centre, University of Glasgow, Glasgow G12 8TA, Scotland, UK.
J Neuroimmunol. 2008 Sep 15;201-202:172-82. doi: 10.1016/j.jneuroim.2008.05.028. Epub 2008 Jul 29.
Recent research into the Guillain-Barré syndromes (GBS) has focused on anti-ganglioside antibodies that correlate with specific clinical phenotypes. Our increasing understanding of the role of antibodies in mediating GBS has naturally focused our attention on complement involvement in the pathological procession. We have studied the axonal and glial components of the murine motor nerve terminal as a model site of antibody and complement mediated injury. Such studies are providing us with clear information on the molecular components underlying our clinicopathological model for GBS and have lead us to the testing of emerging complement therapeutics that are potentially suitable for human use.
近期对吉兰-巴雷综合征(GBS)的研究聚焦于与特定临床表型相关的抗神经节苷脂抗体。我们对抗体在介导GBS中作用的日益深入理解,自然而然地将我们的注意力集中到补体在病理过程中的参与情况。我们研究了小鼠运动神经末梢的轴突和神经胶质成分,将其作为抗体和补体介导损伤的模型部位。此类研究为我们提供了关于GBS临床病理模型潜在分子成分的清晰信息,并促使我们对可能适用于人类的新型补体疗法进行测试。