Roche Stéphane, Dauvilliers Yves, Tiers Laurent, Couderc Carine, Piva Marie-Thérèse, Provansal Monique, Gabelle Audrey, Lehmann Sylvain
CHU Montpellier, Laboratoire de Biochimie, Hôpital St. Eloi, Montpellier, F-34000, France.
J Immunol Methods. 2008 Sep 30;338(1-2):75-8. doi: 10.1016/j.jim.2008.07.002. Epub 2008 Jul 24.
Detection of autoantibodies, which are involved in tissue injury and/or the reporters from the immune system of various pathologic events, has an important potential for diagnosis, prognosis, disease staging and treatment selection. This explains the interest for new proteomics technologies, such as the high-density protein microarray used here, that allow a high-throughput, multiplexed and sensitive detection of specific autoantibodies. So far, most of the research has been performed on blood. In this note, we focus on the cerebrospinal fluid in an attempt to address autoimmune events associated with neurological disorders. Importantly, the cerebrospinal fluid is quite different from the blood in terms of protein composition and concentration. We had therefore to adapt the available blood protocols. We present here the result of our optimization that will be useful to carry out full scale immunological studies of the cerebrospinal fluid using high-density protein microarrays.
自身抗体参与组织损伤和/或各种病理事件免疫系统的报告,其检测在诊断、预后、疾病分期和治疗选择方面具有重要潜力。这解释了人们对新蛋白质组学技术的兴趣,比如本文使用的高密度蛋白质微阵列,它能对特定自身抗体进行高通量、多重和灵敏的检测。到目前为止,大多数研究都是在血液中进行的。在本报告中,我们聚焦于脑脊液,试图解决与神经疾病相关的自身免疫事件。重要的是,脑脊液在蛋白质组成和浓度方面与血液有很大不同。因此,我们必须调整现有的血液检测方案。我们在此展示优化结果,这将有助于使用高密度蛋白质微阵列对脑脊液进行全面的免疫学研究。