• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

重症肌无力患者体内是否存在针对抗乙酰胆碱受体抗体的自发性抗独特型抗体?

Are spontaneous anti-idiotypic antibodies against anti-acetylcholine receptor antibodies present in myasthenia gravis?

作者信息

Vincent A C

机构信息

Department of Neurological Sciences, Royal Free Hospital School of Medicine, London, UK.

出版信息

J Autoimmun. 1988 Apr;1(2):131-42. doi: 10.1016/0896-8411(88)90021-2.

DOI:10.1016/0896-8411(88)90021-2
PMID:3252806
Abstract

The presence of anti-acetylcholine receptor anti-idiotypic antibodies in sera from 102 myasthenia gravis patients and from 33 first-degree relatives was investigated by: (a) Enzyme linked immunosorbent assay (ELISA) using monoclonal antibodies raised against human acetylcholine receptor, (b) immunoprecipitation of 125I-monoclonal anti-acetylcholine receptor antibodies; (c) inhibition of anti-acetylcholine receptor monoclonal antibody binding to the receptor and/or (d) inhibition of autologous and heterologous anti-acetylcholine receptor antibody binding to the receptor. No clear evidence for the presence of abnormal levels of spontaneous anti-idiotypic antibodies to anti-acetylcholine receptor antibodies was found.

摘要

通过以下方法对102例重症肌无力患者和33例一级亲属血清中抗乙酰胆碱受体抗独特型抗体的存在情况进行了研究:(a) 使用针对人乙酰胆碱受体产生的单克隆抗体进行酶联免疫吸附测定(ELISA);(b) 对125I-单克隆抗乙酰胆碱受体抗体进行免疫沉淀;(c) 抑制抗乙酰胆碱受体单克隆抗体与受体的结合,和/或(d) 抑制自身和异源抗乙酰胆碱受体抗体与受体的结合。未发现存在异常水平的抗乙酰胆碱受体抗体自发抗独特型抗体的明确证据。

相似文献

1
Are spontaneous anti-idiotypic antibodies against anti-acetylcholine receptor antibodies present in myasthenia gravis?重症肌无力患者体内是否存在针对抗乙酰胆碱受体抗体的自发性抗独特型抗体?
J Autoimmun. 1988 Apr;1(2):131-42. doi: 10.1016/0896-8411(88)90021-2.
2
Search for cross-reactive idiotypes on monoclonal and myasthenia gravis acetylcholine receptor antibodies.
Autoimmunity. 1992;12(1):53-60. doi: 10.3109/08916939209146130.
3
Anti-acetylcholine receptor antibody related idiotypes in myasthenia gravis.重症肌无力中抗乙酰胆碱受体抗体相关独特型
J Autoimmun. 1988 Feb;1(1):63-72. doi: 10.1016/0896-8411(88)90077-7.
4
Anti-idiotypic antibodies, acetylcholine receptor antibodies and disturbed neuromuscular function in healthy relatives to patients with myasthenia gravis.重症肌无力患者健康亲属中的抗独特型抗体、乙酰胆碱受体抗体与神经肌肉功能紊乱
J Neuroimmunol. 1985 Jul;9(1-2):41-53. doi: 10.1016/s0165-5728(85)80005-9.
5
Anti-idiotypic antibodies to anti-acetylcholine receptor antibody: characterization by ELISA and immunoprecipitation assays.
J Neuroimmunol. 1986 Sep;12(3):205-14. doi: 10.1016/s0165-5728(86)80004-2.
6
Acetylcholine receptor antibodies and anti-idiotypic antibodies produced in blood lymphocyte cultures from patients with myasthenia gravis.重症肌无力患者血液淋巴细胞培养物中产生的乙酰胆碱受体抗体和抗独特型抗体。
Scand J Immunol. 1986 Jun;23(6):655-62. doi: 10.1111/j.1365-3083.1986.tb02001.x.
7
Monoclonal anti-acetylcholine receptor antibodies as probes for human acetylcholine-receptor in myasthenia gravis.单克隆抗乙酰胆碱受体抗体作为重症肌无力患者人类乙酰胆碱受体的探针。
J Recept Res. 1988;8(1-4):143-59. doi: 10.3109/10799898809048984.
8
Idiotypic network in myasthenia gravis demonstrated by human monoclonal B-cell lines.人单克隆B细胞系证实的重症肌无力独特型网络
Scand J Immunol. 1987 Nov;26(5):573-8. doi: 10.1111/j.1365-3083.1987.tb02291.x.
9
Idiotypes and anti-idiotypes of human autoantibodies to the acetylcholine receptor in myasthenia gravis.重症肌无力中针对乙酰胆碱受体的人自身抗体的独特型和抗独特型
Monogr Allergy. 1987;22:57-70.
10
Auto-anti-idiotypic immunity and acetylcholine receptors.
Concepts Immunopathol. 1986;3:285-310.

引用本文的文献

1
John Newsom-Davis: clinician-scientist and so much more.约翰·纽瑟姆-戴维斯:临床科学家,远不止于此。
Brain. 2011 Dec;134(Pt 12):3755-74. doi: 10.1093/brain/awr284.
2
Clinical implementation of anti-acetylcholine receptor antibodies.抗乙酰胆碱受体抗体的临床应用
J Neurol Neurosurg Psychiatry. 1993 May;56(5):496-504. doi: 10.1136/jnnp.56.5.496.