Harling-Berg C J, Knopf P M, Cserr H F
Section of Physiology, Brown University, Providence, RI 02912.
J Neuroimmunol. 1991 Dec;35(1-3):45-51. doi: 10.1016/0165-5728(91)90160-9.
We have evaluated the antibody and the effector T-cell responses to a single cerebrospinal fluid (CSF) infusion of myelin basic protein (MBP) in Lewis rats by measuring serum anti-MBP antibodies and clinical signs of experimental autoimmune encephalomyelitis (EAE), respectively. Some rats developed anti-MBP antibodies, but none manifested EAE in response to the primary infusion. Antibody responses to an EAE challenge 3 weeks after CSF infusion were normal, but clinical symptoms of EAE were markedly suppressed. Brain trauma at the time of MBP pretreatment enhanced this suppression. The CSF route of MBP administration is more effective in inducing suppression of EAE than peripheral routes.
我们通过分别测量血清抗髓鞘碱性蛋白(MBP)抗体和实验性自身免疫性脑脊髓炎(EAE)的临床症状,评估了Lewis大鼠单次经脑脊液(CSF)注入髓鞘碱性蛋白(MBP)后的抗体和效应T细胞反应。一些大鼠产生了抗MBP抗体,但初次注入后无一表现出EAE。脑脊液注入3周后,对EAE激发的抗体反应正常,但EAE的临床症状明显受到抑制。MBP预处理时的脑外伤增强了这种抑制作用。与外周途径相比,经脑脊液途径给予MBP在诱导EAE抑制方面更有效。