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炎症性脱髓鞘性多发性神经病中自身抗体的调节:自发调节与治疗性调节

Regulation of autoantibodies in inflammatory demyelinating polyneuropathy: spontaneous and therapeutic.

作者信息

Lundkvist I, van Doorn P A, Vermeulen M, van Lint M, van Rood J J, Brand A

机构信息

Department of Immunohematology and Bloodbank, University Hospital, Leiden, The Netherlands.

出版信息

Immunol Rev. 1989 Aug;110:105-17. doi: 10.1111/j.1600-065x.1989.tb00029.x.

Abstract

We have analyzed the role and regulation of autoantibodies in inflammatory demyelinating polyneuropathy (GBS/CIDP). The clinical significance of pathogenic autoantibodies to peripheral nerve tissue is suggested by the beneficial response of many of these patients to plasmapheresis and treatment with high doses of polyspecific IVIgG. Recovery, whether spontaneous or therapeutically-induced, is associated with anti-idiotypic suppression of the antoantibodies. Preliminary results suggest that these autoantibodies share cross-reactive idiotypes or, alternatively, that the regulatory anti-idiotypic antibodies are multireactive.

摘要

我们分析了自身抗体在炎性脱髓鞘性多发性神经病(吉兰 - 巴雷综合征/慢性炎性脱髓鞘性多发性神经根神经病)中的作用及调节机制。许多此类患者对血浆置换和高剂量多特异性静脉注射免疫球蛋白治疗的良好反应提示了致病性自身抗体对周围神经组织的临床意义。恢复,无论是自发的还是治疗诱导的,都与自身抗体的抗独特型抑制相关。初步结果表明,这些自身抗体共享交叉反应性独特型,或者,调节性抗独特型抗体具有多反应性。

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