Soukop W, Tschabitscher H
Wien Med Wochenschr. 1986 Sep 30;136(18):477-80.
The number of reports about successful therapeutical application of 7S-immunoglobulins in various auto-immune diseases such as ITP or autoimmune neutropenia or in myasthenia gravis has increased in recent years. Multiple Sclerosis (MS) is an inflammatory demyelinating disease, in which antibodies directed against various components of the myelin sheath play an important pathogenetic part. Increased antibody dependent cytotoxicity has been reported in MS, and myelinotoxic antibodies and a myelination inhibiting factor have been found in acute cases. Lately several authors have tested 7S-immunoglobulins in the treatment of MS. It is still too early for final judgement of the therapeutical efficacy, however, patients suffering from the progressive form of MS with exacerbations showed rather fast improvement of their latest neurological deficits, when treated shortly after a fresh bout. Mechanisms of action which should be taken into consideration include reduced antibody dependent cytotoxicity by surface receptor blocking reduction of the number of circulating myelinotoxic antibodies caused by a negative feed back mechanism, and removal of a neuroelectric inhibiting factor caused by antibodies.
近年来,关于7S免疫球蛋白在多种自身免疫性疾病(如免疫性血小板减少性紫癜、自身免疫性中性粒细胞减少症或重症肌无力)中成功应用于治疗的报道数量有所增加。多发性硬化症(MS)是一种炎症性脱髓鞘疾病,其中针对髓鞘不同成分的抗体在发病机制中起重要作用。在MS中已报道抗体依赖性细胞毒性增加,并且在急性病例中发现了髓鞘毒性抗体和髓鞘形成抑制因子。最近,几位作者对7S免疫球蛋白治疗MS进行了测试。然而,要对治疗效果做出最终判断还为时过早,患有进行性加重型MS的患者在一次新发作后不久接受治疗时,其最近出现的神经功能缺损有相当快的改善。应考虑的作用机制包括通过表面受体阻断减少抗体依赖性细胞毒性、通过负反馈机制减少循环髓鞘毒性抗体的数量以及去除由抗体引起的神经电抑制因子。