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视神经脊髓炎中体液免疫和嗜酸性粒细胞的激活。

Activation of humoral immunity and eosinophils in neuromyelitis optica.

作者信息

Correale Jorge, Fiol Marcela

机构信息

Raúl Carrea Institute for Neurological Research, FLENI, Montañeses 2325 (1428), Buenos Aires, Argentina.

出版信息

Neurology. 2004 Dec 28;63(12):2363-70. doi: 10.1212/01.wnl.0000148481.80152.bf.

Abstract

OBJECTIVE

To study immunologic alterations in patients with neuromyelitis optica (NMO).

METHODS

The authors studied 8 patients with NMO together with 16 healthy subjects, 16 patients with relapsing remitting multiple sclerosis (RRMS), and 16 patients with secondary progressive MS (SPMS), matched for age and sex, as controls. Because recent histopathologic studies have demonstrated that active NMO lesions consist of perivascular immunoglobulin (Ig) deposition and eosinophil infiltration, IL-5, IL-6, IL-12, IgG, and IgM production by anti-myelin oligodendrocyte glycoprotein (MOG) mononuclear cells in peripheral blood and CSF were selected for study using ELISPOT. Eotaxin-2 (Eo-2) and eotaxin-3 (Eo-3) levels were also assessed using ELISA and eosinophil cationic protein (ECP) levels by radioimmunoassay.

RESULTS

MOG-specific responses in CSF showed significant increase in IL-5, IL-6, IgG, and IgM secreting cells in NMO patients compared with patients with RRMS, SPMS and healthy subjects. Interestingly, numbers of IgM secreting cells were significantly higher than identical specificity IgG secreting ones. Moreover, CSF Eo-2, Eo-3, and ECP levels were also significantly higher in NMO patients compared to all three control populations. Anti-MOG IL-12 secreting cells were increased in CSF and peripheral blood from NMO, RRMS, and SPMS patients when compared to healthy subjects.

CONCLUSIONS

These observations suggest that neuromyelitis optica is associated with a major humoral immune response (particularly anti-MOG IgM production) and eosinophil activation present exclusively in CSF.

摘要

目的

研究视神经脊髓炎(NMO)患者的免疫改变。

方法

作者研究了8例NMO患者,并将年龄和性别匹配的16名健康受试者、16例复发缓解型多发性硬化症(RRMS)患者和16例继发进展型MS(SPMS)患者作为对照。由于最近的组织病理学研究表明,活动性NMO病变由血管周围免疫球蛋白(Ig)沉积和嗜酸性粒细胞浸润组成,因此选择使用酶联免疫斑点法(ELISPOT)研究外周血和脑脊液中抗髓鞘少突胶质细胞糖蛋白(MOG)单核细胞产生的白细胞介素-5(IL-5)、白细胞介素-6(IL-6)、白细胞介素-12(IL-12)、IgG和IgM。还使用酶联免疫吸附测定(ELISA)评估嗜酸性粒细胞趋化因子-2(Eo-2)和嗜酸性粒细胞趋化因子-3(Eo-3)水平,并通过放射免疫测定法评估嗜酸性粒细胞阳离子蛋白(ECP)水平。

结果

与RRMS患者、SPMS患者和健康受试者相比,NMO患者脑脊液中MOG特异性反应显示,分泌IL-5、IL-6、IgG和IgM的细胞显著增加。有趣的是,分泌IgM的细胞数量显著高于相同特异性分泌IgG的细胞。此外,与所有三个对照组相比,NMO患者脑脊液中的Eo-2、Eo-3和ECP水平也显著更高。与健康受试者相比,NMO、RRMS和SPMS患者脑脊液和外周血中分泌抗MOG IL-12的细胞增加。

结论

这些观察结果表明,视神经脊髓炎与主要的体液免疫反应(特别是抗MOG IgM产生)以及仅存在于脑脊液中的嗜酸性粒细胞激活有关。

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