Center for Neurologic Diseases, Brigham and Women's Hospital, Harvard Medical School, 77 Avenue Louis Pasteur, Boston, MA 02115, USA.
J Neuroimmunol. 2012 Jul 15;248(1-2):53-7. doi: 10.1016/j.jneuroim.2012.01.002. Epub 2012 May 12.
Multiple sclerosis (MS) is an autoimmune disease that targets the central nervous system (CNS). MS initially follows a relapsing-remitting course (RRMS) in which acute attacks are followed by a complete recovery. Eventually, 65% of the RRMS patients go on to develop secondary progressive MS (SPMS), characterized by the progressive and irreversible accumulation of neurological disability. It has been proposed that the transition from RRMS to SPMS results from changes in the nature of the inflammatory response and the progressive accumulation of neurodegeneration. To date, however, there is no reliable method to monitor the activity of the different immune and neurodegenerative processes that contribute to MS pathology. Thus, there is a need for biomarkers useful for the diagnosis, treatment and monitoring of MS patients. In this review, we discuss the potential use of lipids and the immune response against them as biomarkers of inflammation and neurodegeneration for MS.
多发性硬化症 (MS) 是一种自身免疫性疾病,靶向中枢神经系统 (CNS)。MS 最初表现为复发缓解型 (RRMS),在这种疾病中,急性发作后会完全恢复。最终,65%的 RRMS 患者会发展为继发进展型 MS (SPMS),其特征是神经功能障碍的进行性和不可逆转的累积。有人提出,RRMS 向 SPMS 的转变是由于炎症反应性质的变化和神经退行性变的进行性累积所致。然而,迄今为止,尚无可靠的方法来监测导致 MS 病理学的不同免疫和神经退行性过程的活性。因此,需要有用的生物标志物来诊断、治疗和监测 MS 患者。在这篇综述中,我们讨论了脂质及其免疫反应作为 MS 炎症和神经退行性变的生物标志物的潜在用途。