Brunmark Charlott, Runström Anna, Ohlsson Lennart, Sparre Birgitta, Brodin Thomas, Aström Mikael, Hedlund Gunnar
Active Biotech Research AB, Box 724, S-220 07, Lund, Sweden.
J Neuroimmunol. 2002 Sep;130(1-2):163-72. doi: 10.1016/s0165-5728(02)00225-4.
A new orally active drug, laquinimod (ABR-215062), was shown to completely inhibit the development of murine acute experimental autoimmune encephalomyelitis (EAE). Furthermore, leukocyte infiltration into the central nervous system (CNS) was abolished in the laquinimod-treated animals. By direct comparison based on dose and total exposure, laquinimod was approximately 20 times more potent than the immunomodulator roquinimex. Laquinimod also had clear therapeutic effect when given after clinical onset in a chronic relapsing EAE model. It therefore represents a new orally active immunoregulatory drug without general immunosuppressive properties for the treatment of the autoimmune disease multiple sclerosis.
一种新型口服活性药物拉喹莫德(ABR - 215062)被证明能完全抑制小鼠急性实验性自身免疫性脑脊髓炎(EAE)的发展。此外,在接受拉喹莫德治疗的动物中,白细胞向中枢神经系统(CNS)的浸润被消除。通过基于剂量和总暴露量的直接比较,拉喹莫德的效力比免疫调节剂罗喹美克强约20倍。在慢性复发性EAE模型中,拉喹莫德在临床发病后给药也具有明显的治疗效果。因此,它代表了一种新型的口服活性免疫调节药物,用于治疗自身免疫性疾病多发性硬化症时无全身免疫抑制特性。