Investigation on the immune reactions against complex antigens including gangliosides in the neuroimmunological diseases
Investigation on the immune reactions against complex antigens including gangliosides in the neuroimmunological diseases
批准号:
16590854
负责人:
KUSUNOKI Susumu
金额:
$2.24万
依托单位:
依托单位国家:
日本
项目类别:
Grant-in-Aid for Scientific Research (C)
财政年份:
2004
资助国家:
日本
项目状态:
已结题
起止时间:
2004 至 2005
中文摘要
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英文摘要
Antiganglioside antibodies are frequently present in sera from patients with neuroimmunological diseases as Guillain Barre syndrome (GBS) and Miller Fisher syndrome (MFS). Each ganglioside coexists with phospholipids and other gangliosides in the plasma membrane. We investigated antibody reactivities against complex antigens composed of a ganglioside and a phospholipid or those composed of two species of gangliosides. Anti-GM1 IgG antibodies in GBS had stronger binding activities against a mixture of GM1 and such phospholipids as phosphatidic acid than against GM1 alone. However, such increase was not observed in anti-GQ1b IgG antibodies in MFS. This may be due to the difference in the amount of the negatively-charged sialic acid that each antigen has ; GM1 has one sialic acid whereas GQ1b has four sialic acids. Some GBS patients had the antibodies specific to the ganglioside complex, which is composed of two different gangliosides. Among them, the antibodies specific to GD1a-GD1b complex and/or GD1b-GT1b complex are associated with severe GBS requiring artificial ventilation. In addition, some MFS patients had the antibodies against ganglioside complexes that include GQ1b. For elucidating the pathogenetic roles of the antiganglioside antibodies in neuroimmunological diseases, we should pay attention on the antibody activities against those complex antigens. Investigating antibodies against the complex antigens also may be useful for diagnosis of neuroimmunological diseases as GBS and MFS.
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Harmful effects of anti-GalNAc-GD1a antibodies and TNF-alpha on rat dorsal root ganglia.
抗 GalNAc-GD1a 抗体和 TNF-α 对大鼠背根神经节的有害影响。
DOI:
--
发表时间:
2005
期刊:
Periph Nerv Sys 10
影响因子:
--
作者:
[Kamakura K, Kaida K, Kusunoki S, Miyamoto N, Masaki T, Nakamura R, Motoyoshi K, Fukuda J.]
通讯作者:
Fukuda J.
DOI:
10.1016/j.jneuroim.2004.09.018
发表时间:
2005-02-01
期刊:
JOURNAL OF NEUROIMMUNOLOGY
影响因子:
3.3
作者:
[Hirakawa, M, Morita, D, Kusunoki, S]
通讯作者:
Kusunoki, S
DOI:
10.1212/01.wnl.0000113718.27729.43
发表时间:
2004-03-09
期刊:
NEUROLOGY
影响因子:
9.9
作者:
[Kaida, K, Kusunoki, S, Kanazawa, I]
通讯作者:
Kanazawa, I
Behcet disease presenting with neurological complications immediately after conversion from conventional cyclosporin A to microemulsion formulation.
从传统环孢菌素 A 转为微乳制剂后,白塞病立即出现神经系统并发症。
DOI:
--
发表时间:
2005
期刊:
Intern Med 44
影响因子:
--
作者:
[Mitsui Y, Mitsui M, Urakami R, Kihara M, Takahashi M, Kusunoki S.]
通讯作者:
Kusunoki S.
DOI:
10.1212/01.wnl.0000178802.38268.1e
发表时间:
2005-10-11
期刊:
NEUROLOGY
影响因子:
9.9
作者:
[Uchibori, A, Sakuta, M, Chiba, A]
通讯作者:
Chiba, A
共 10 条
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Analysis of negative regulators of B lymphocyte responses to glycoconjugates in neuroimmunological diseases
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Analysis of the neuropathogenic mechanisms induced by the antiganglioside antibodies : the effect on signal transduction in neurons
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Analysis of immunoreactivity against glycoproteins with disialosyl residue in neuroimmunological diseases
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财政年份:2006
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依托单位:
Investigation on the significance of the epitope formed by ganglioside and phospholipid in neuroimmunological diseases
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资助金额:$2.18万
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财政年份:2002
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依托单位:
Development of axonal degeneration by passive transfer of antiganglioside antibody and therapeutic trial for it.
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批准号:12670595
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财政年份:2000
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依托单位:
Identification of a ganglioside localized in paranodal region of peripheral nerve and induction of experimental autoimmune neuropathy
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财政年份:1998
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Investigation on the pathogenetic mechanism of GD1b-induced experimental neuropathy and approach to effective treatment
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批准号:08670695
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财政年份:1996
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依托单位:
Identification and localization of minor glycolipid antigens recognized by serum antibody in Guillain-Barre' syndrome
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负责人:KUSUNOKI Susumu
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依托单位:
国内基金
海外基金
Ganglioside-CD44信号通路在PEMFs对小鼠缺血心肌血管生成影响中的作用及其机制研究
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批准号:81572231
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项目类别:面上项目
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资助金额:57.0万元
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批准年份:2015
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负责人:魏全
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依托单位: