Induction of a non-encephalitogenic type 2 T helper-cell autoimmune response in multiple sclerosis after administration of an altered peptide ligand in a placebo-controlled, randomized phase II trial

被引:433
作者
Kappos, L
Comi, G
Panitch, H
Oger, J
Antel, J
Conlon, P
Steinman, L [1 ]
机构
[1] Stanford Univ, Sch Med, Beckman Ctr B002, Dept Neurol Neurosci, Stanford, CA 94305 USA
[2] Univ Basel Hosp, Dept Neurol, CH-4031 Basel, Switzerland
[3] San Raffaele Sci Inst, Dept Neurol, I-20132 Milan, Italy
[4] Univ Maryland, Sch Med, Dept Neurol, Baltimore, MD 21201 USA
[5] Univ British Columbia, Div Neurol, Vancouver, BC V6T 2B5, Canada
[6] McGill Univ, Dept Neurol & Neurosurg, Montreal, PQ H3A 2B4, Canada
[7] McGill Univ, Montreal Neurol Inst, Dept Neurol & Neurosurg, Neuroimmunol Unit, Montreal, PQ H3A 2B4, Canada
[8] Neurocrine Biosci, San Diego, CA 92121 USA
关键词
D O I
10.1038/80525
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
In this 'double-blind', randomized, placebo-controlled phase II trial, we compared an altered peptide ligand of myelin basic protein with placebo, evaluating their safety and influence on magnetic resonance imaging in relapsing-remitting multiple sclerosis. A safety board suspended the trial because of hypersensitivity reactions in 9% of the patients. There were no increases in either clinical relapses or in new enhancing lesions in any patient, even those with hypersensitivity reactions. Secondary analysis of those patients completing the study showed that the volume and number of enhancing lesions were reduced at a dose of 5 mg. There was also a regulatory type 2 T helper-cell response to altered peptide ligand that cross-reacted with the native peptide.
引用
收藏
页码:1176 / 1182
页数:7
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