Kappos L
Clinical Research Unit for Multiple Sclerosis, Max-Planck-Society, Würzburg, F.R.G.
J Neuroimmunol. 1988 Dec;20(2-3):261-8. doi: 10.1016/0165-5728(88)90173-7.
Although clinical trials in multiple sclerosis are extremely difficult to conduct because of the unpredictable course of the disease and the problem of defining and monitoring disease activity, some controlled and several uncontrolled studies suggest that global immunosuppression may result in a small but beneficial effect. After some methodological considerations the results of recent trials are reviewed especially those concerned with the use of cyclophosphamide, azathioprine and cyclosporine. Major improvements in our ability to slow-down disease progression may develop through the administration of more sophisticated, phase-adapted therapies using combinations of different immunosuppressive and modulating agents which should be applied in earlier phases of the disease. Improved monitoring of disease evolution by the addition of magnetic resonance imaging to current clinical scales and by ameliorated immunological techniques is an indispensable prerequisite of any further therapeutic progress.
由于多发性硬化症病程不可预测,以及疾病活动的定义和监测问题,开展多发性硬化症的临床试验极其困难。然而,一些对照研究和若干非对照研究表明,全身性免疫抑制可能会产生虽小但有益的效果。在经过一些方法学考量后,本文回顾了近期试验的结果,尤其是那些与环磷酰胺、硫唑嘌呤和环孢素使用相关的试验结果。通过使用不同免疫抑制和调节药物的组合,实施更复杂、分阶段适配的疗法,并在疾病的早期阶段应用,我们减缓疾病进展的能力可能会取得重大进展。通过在当前临床量表中加入磁共振成像以及改进免疫技术来更好地监测疾病进展,是任何进一步治疗进展不可或缺的前提条件。