Macpherson C F, Armstrong H, Tan O
Immunology. 1977 Aug;33(2):161-6.
Pretreatment of Hartley guinea-pigs with three injections of 100 microgram of the purified bovine spinal cord protein, (SCP), protected tham from clinical experimental allergic encephalitis (EAE) when they were subsequently challenged with 50 microgram of purified bovine myelin basic protein (MyBP) in Freund's complete adjuvant (FCA). The length of the optimum pretreated schedule was found to be 1 week and the animals were fully protected for 2 weeks. Protection declined thereafter so that by 4 weeks following pretreatment only 40% of the animals were protected. The protected state could be restored several weeks after it had lapsed by repeating the treatment with SCP. Immature animals did not respond well to pretreatment with SCP. Evidence was presented to indicate that specific, non-specific immune suppression or anti-SCP IgG were not involved to a significant extent in protection. SCP-treated guinea-pigs regularly displayed delayed skin hypersensitivity to MyBP after sensitization but there was no correlation between the degree of cutaneous reactivity and protection from disease. Because SCP is localized in the nerve axon, the speculation was advanced that anti-SCP blocking factors might be responsible for preserving axonal function in SCP-treated animals sensitized with MyBP.
用三次注射100微克纯化牛脊髓蛋白(SCP)对Hartley豚鼠进行预处理,当它们随后用50微克纯化牛髓鞘碱性蛋白(MyBP)加弗氏完全佐剂(FCA)进行攻击时,可保护它们免受临床实验性变应性脑脊髓炎(EAE)。发现最佳预处理方案的时长为1周,动物可获得2周的完全保护。此后保护作用下降,以至于预处理后4周时只有40%的动物受到保护。保护状态在消退数周后,通过重复SCP治疗可得以恢复。未成熟动物对SCP预处理反应不佳。有证据表明,特异性、非特异性免疫抑制或抗SCP IgG在保护过程中并未起显著作用。经SCP处理的豚鼠致敏后对MyBP经常表现出迟发型皮肤超敏反应,但皮肤反应程度与疾病保护之间并无相关性。由于SCP定位于神经轴突,有人提出推测,抗SCP阻断因子可能是在用MyBP致敏的经SCP处理动物中维持轴突功能的原因。