Brimberg Lior, Mader Simone, Fujieda Yuichiro, Arinuma Yoshiyuki, Kowal Czeslawa, Volpe Bruce T, Diamond Betty
Feinstein Institute for Medical Research, Manhasset, NY, USA.
Feinstein Institute for Medical Research, Manhasset, NY, USA.
Trends Immunol. 2015 Nov;36(11):709-724. doi: 10.1016/j.it.2015.09.008. Epub 2015 Oct 19.
The brain is normally sequestered from antibody exposure by the blood brain barrier. However, antibodies can access the brain during fetal development before the barrier achieves full integrity, and in disease states when barrier integrity is compromised. Recent studies suggest that antibodies contribute to brain pathology associated with autoimmune diseases such as systemic lupus erythematosus and neuromyelitis optica, and can lead to transient or permanent behavioral or cognitive abnormalities. We review these findings here and examine the circumstances associated with antibody entry into the brain, the routes of access and the mechanisms that then effect pathology. Understanding these processes and the nature and specificity of neuronal autoantibodies may reveal therapeutic strategies toward alleviating or preventing the neurological pathologies and behavioral abnormalities associated with autoimmune disease.
正常情况下,血脑屏障可使大脑免受抗体的影响。然而,在胎儿发育期间,血脑屏障尚未完全形成时,以及在疾病状态下血脑屏障完整性受损时,抗体能够进入大脑。最近的研究表明,抗体与自身免疫性疾病(如系统性红斑狼疮和视神经脊髓炎)相关的脑部病变有关,并可导致短暂或永久性的行为或认知异常。我们在此回顾这些发现,并探讨与抗体进入大脑相关的情况、进入途径以及随后影响病变的机制。了解这些过程以及神经元自身抗体的性质和特异性,可能会揭示出减轻或预防与自身免疫性疾病相关的神经病变和行为异常的治疗策略。