Lund Brett T, Chakryan Yervand, Ashikian Nazely, Mnatsakanyan Lilit, Bevan Carolyn J, Aguilera Rodrigo, Gallaher Tim, Jakowec Michael W
Department of Neurology, Keck School of Medicine, University of Southern California, McKibben Annex, Room 246, 1333 San Pablo Street, Los Angeles, California 90033, United States.
J Neurol Sci. 2006 Nov 15;249(2):122-34. doi: 10.1016/j.jns.2006.05.066. Epub 2006 Jul 13.
Multiple Sclerosis is an autoimmune disease directed against myelin proteins. The etiology of MS is poorly defined though, with no definitive causative agent yet identified. It has been hypothesized that MS may be a multifactorial disease resulting in the same end product: the destruction of myelin by the immune system. In this report we describe a potential role for heat shock proteins in the pathogenesis of MS. We isolated Hsp70 from the normal appearing white matter of both MS and normal human brain and found this was actively associated with, among other things, immunodominant MBP peptides. Hsp70-MBP peptide complexes prepared in vitro were shown to be highly immunogenic, with adjuvant-like effects stimulating MBP peptide-specific T cell lines to respond to normally sub-optimal concentrations of peptide. This demonstration of a specific interaction between Hsp70 and different MBP peptides, coupled with the adjuvanticity of this association is suggestive of a possible role for Hsp70 in the immunopathology associated with MS.
多发性硬化症是一种针对髓鞘蛋白的自身免疫性疾病。然而,MS的病因尚不明确,尚未确定明确的致病因素。据推测,MS可能是一种多因素疾病,最终导致相同的结果:免疫系统破坏髓鞘。在本报告中,我们描述了热休克蛋白在MS发病机制中的潜在作用。我们从MS患者和正常人大脑外观正常的白质中分离出Hsp70,发现它与免疫显性MBP肽等物质有活跃的关联。体外制备的Hsp70-MBP肽复合物具有高度免疫原性,具有佐剂样作用,可刺激MBP肽特异性T细胞系对通常次优浓度的肽作出反应。Hsp70与不同MBP肽之间特异性相互作用的证明,以及这种关联的佐剂活性,提示Hsp70在与MS相关的免疫病理学中可能发挥作用。