Takamori M, Ide Y
Department of Neurology, Kanazawa University School of Medicine, Japan.
Transfus Sci. 1996 Sep;17(3):445-53. doi: 10.1016/0955-3886(96)00028-8.
In short-term therapy for myasthenia gravis caused by an antibody-mediated attack on the acetylcholine receptor (AChR) in skeletal muscle, a specific system for antibody removal, the use of tryptophan-bound immunoadsorbent and synthetic AChR peptide-bound immunoadsorbent, offers advantages over plasma exchange. These two types of immunoadsorption provided selective or semi-selective removal of pathogenic substances from the circulation without the use of plasma products, and minimized side-effects. A difficulty is that the former removed about 65% of the total IgG, and the latter removed only a fraction of the pathogenic antibodies. In neither case can a radical method of treatment for myasthenia gravis be expected. Hopefully, an adsorbent which has a well-balanced bioimmunological specific binding reaction and physicochemical adsorptive affinity will be developed in the future.
在针对由抗体介导攻击骨骼肌中乙酰胆碱受体(AChR)所引起的重症肌无力的短期治疗中,一种特定的抗体清除系统,即使用色氨酸结合免疫吸附剂和合成AChR肽结合免疫吸附剂,比血浆置换具有优势。这两种免疫吸附方法能够在不使用血浆制品的情况下,从循环中选择性或半选择性地清除致病物质,并将副作用降至最低。一个难题是,前者能清除约65%的总IgG,而后者仅能清除一小部分致病抗体。在这两种情况下,都无法期待一种能根治重症肌无力的方法。有望在未来研发出一种具有平衡的生物免疫特异性结合反应和物理化学吸附亲和力的吸附剂。