Miller-Fischer综合征,抗gq1b和空肠弯曲杆菌:1 .观察场合

G Laplatte , C Bouterra , A Itani , K Kuteifan , A.M Gutbub
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引用次数: 2

摘要

报告1例米勒-费舍尔综合征伴神经节苷脂GQ 1b血清抗体。虽然没有引起腹部症状或腹泻,但发现空肠弯曲杆菌抗体升高。静脉注射免疫球蛋白可迅速改善病情。先前的出版物报道了Miller-Fischer综合征患者神经节苷脂GQ 1b的IgG抗体升高,而在其他神经系统疾病和正常对照中未发现。这种高特异性可能对非典型病例有帮助。gq1b在动眼肌淋巴结和小脑的显著分布可能是米勒-费舍尔综合征的主要特征共济失调和眼麻痹的原因。此外,抗gq 1b抗体识别空肠梭菌表面表位,提示分子模仿。因此,弯曲杆菌感染可能引发免疫紊乱。然而,其他因素被发现可以解释疾病的发病,无论它们与宿主或细菌的关系如何。
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Syndrome de Miller-Fischer, anticorps anti-GQ 1b et Campylobacter jejuni: à l'occasion d'une observation

A case of Miller-Fischer syndrome is reported with serum antibody to ganglioside GQ 1b. Though no abdominal signs or diarrhoea have been elicited, elevated antibody titles to Campylobacter jejuni were found. Rapid improvement is obtained with intraveinous immunoglobulins. Previous publications report elevated titles of IgG antibody to ganglioside GQ 1b in patients with the Miller-Fischer syndrome whereas they are not found in other neurologic conditions and normal controls. This high specificity might he helpful in atypical cases. Prominent distribution of GQ 1b in oculomotor nodes and cerebellum could account for ataxia and ophtalmoplegia, main features of the Miller-Fischer syndrome. Moreover, anti-GQ 1b antibody recognize surface epitopes on C. jejuni, suggesting molecular mimicry. Thus, initiation of immunologic disorder might follow Campylobacter infection. However, other factors were found to explain onset of the disease whatever their correlation with host or bacteria.

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