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[多发性硬化症的发病机制。多发性硬化症中淋巴细胞对髓鞘碱性蛋白的抗体依赖性细胞毒性]

[Pathogenesis of multiple sclerosis. Antibody dependent cytotoxicity of lymphocytes against myelin basic proteins in multiple sclerosis].

作者信息

Frick E, Stickl H

出版信息

Fortschr Med. 1977 Oct 6;95(37):2235-41.

PMID:914178
Abstract

In 79 of 100 patients with multiple sclerosis, serum antibodies of the IgG type were demonstrated which render normal lymphocytes cytotoxic against basic protein of myelin. In 11 cerebrospinal fluids which were tested the antibody was also found. The method used was the release of 51Cr from chicken erythrocytes coated with antigen. The antibody-dependent lymphocyte cytotoxicity is related to the degree of activity of the disease and not to the evolution of the disease or its course. As the disease worsens, the frequency of positive reactions is higher than in inactive stages. The immunological reaction is very specific for multiple sclerosis, in patients with other neurological disorders only 5% had positive findings. The antibody-dependent cytotoxicity of lymphocytes against basic protein of myelin may be attributed with a certain diagnostic significance. The reaction seems suitable for the supervision of the course of multiple sclerosis and to check the effect of therapeutic measures. The antibody-dependent lymphocyte cytotoxicity against basic protein of myelin is considered to be significant in the pathogenesis of multiple sclerosis.

摘要

在100例多发性硬化症患者中,有79例检测到IgG型血清抗体,该抗体可使正常淋巴细胞对髓鞘碱性蛋白产生细胞毒性。在检测的11份脑脊液中也发现了这种抗体。所采用的方法是从包被有抗原的鸡红细胞中释放51Cr。抗体依赖性淋巴细胞细胞毒性与疾病的活动程度有关,而与疾病的进展或病程无关。随着疾病恶化,阳性反应的频率高于非活动期。这种免疫反应对多发性硬化症具有高度特异性,在其他神经系统疾病患者中只有5%有阳性结果。淋巴细胞对髓鞘碱性蛋白的抗体依赖性细胞毒性可能具有一定的诊断意义。该反应似乎适用于监测多发性硬化症的病程以及检查治疗措施的效果。淋巴细胞对髓鞘碱性蛋白的抗体依赖性细胞毒性被认为在多发性硬化症的发病机制中具有重要意义。

相似文献

1
[Pathogenesis of multiple sclerosis. Antibody dependent cytotoxicity of lymphocytes against myelin basic proteins in multiple sclerosis].[多发性硬化症的发病机制。多发性硬化症中淋巴细胞对髓鞘碱性蛋白的抗体依赖性细胞毒性]
Fortschr Med. 1977 Oct 6;95(37):2235-41.
2
[The pathogenesis of multiple sclerosis. Cytotoxic antibodies against myelin sheath tissue in multiple sclerosis].[多发性硬化症的发病机制。多发性硬化症中针对髓鞘组织的细胞毒性抗体]
Fortschr Med. 1976 Jun 10;94(17):1019-24.
3
Antimyelin basic protein and antimyelin antibody-producing cells in multiple sclerosis.多发性硬化症中的抗髓鞘碱性蛋白和产生抗髓鞘抗体的细胞
Ann Neurol. 1990 Feb;27(2):132-6. doi: 10.1002/ana.410270207.
4
[Immunologic multiple sclerosis research].
Wien Med Wochenschr. 1985 Jan 31;135(1-2):8-9.
5
In vitro cell-mediated immunity of cerebrospinal-fluid lymphocytes to myelin basic protein in primary demyelinating diseases.原发性脱髓鞘疾病中脑脊液淋巴细胞对髓鞘碱性蛋白的体外细胞介导免疫
N Engl J Med. 1977 Oct 20;297(16):850-3. doi: 10.1056/NEJM197710202971602.
6
CD16+ gammadelta T cells mediate antibody dependent cellular cytotoxicity: potential mechanism in the pathogenesis of multiple sclerosis.CD16+ γδ T细胞介导抗体依赖性细胞毒性:多发性硬化症发病机制中的潜在机制。
Clin Immunol. 2008 Aug;128(2):219-27. doi: 10.1016/j.clim.2008.03.513. Epub 2008 May 22.
7
T-cell recognition of an immunodominant myelin basic protein epitope in multiple sclerosis.多发性硬化症中免疫显性髓鞘碱性蛋白表位的T细胞识别
Nature. 1990 Jul 12;346(6280):183-7. doi: 10.1038/346183a0.
8
Myelin basic protein-specific T lymphocytes in multiple sclerosis and controls: precursor frequency, fine specificity, and cytotoxicity.
Ann Neurol. 1992 Sep;32(3):330-8. doi: 10.1002/ana.410320305.
9
[Multiple sclerosis and the immune system. Progress and unsolved problems].[多发性硬化症与免疫系统。进展与未解决的问题]
Med Klin. 1978 Dec 15;73(50):1752-67.
10
[Antibodies against encephalitogenic protein and myelin glycoprotein in the cerebrospinal fluid of patients with multiple sclerosis. Effect of encorton treatment on the autoantibody and immune complex levels].
Folia Med Cracov. 1984;25(3-4):307-18.

引用本文的文献

1
Immunological reactions against Mycoplasma pneumoniae in multiple sclerosis: preliminary findings.多发性硬化症中针对肺炎支原体的免疫反应:初步研究结果。
J Neurol. 1983;229(2):103-11. doi: 10.1007/BF00313449.
2
Reactivity of sera and isolated monoclonal IgM from patients with Waldenström's macroglobulinaemia with peripheral nerve myelin.华氏巨球蛋白血症患者血清及分离出的单克隆IgM与周围神经髓鞘的反应性
J Neurol. 1985;232(1):43-8. doi: 10.1007/BF00314040.