Animal model of axonal Guillain-Barré syndrome induced by sensitization with GM1 ganglioside.

Abstract

Some humans develop the axonal form of Guillain-Barré syndrome after receiving bovine brain ganglioside. On sensitization with the ganglioside mixture, all of a group of rabbits injected developed high anti-GM1 IgG antibody titers, flaccid limb weakness of acute onset, and a monophasic illness course. Pathological findings for the peripheral nerves showed predominant Wallerian-like degeneration, with neither lymphocytic infiltration nor demyelination. IgG was deposited on the axons of the anterior roots, and GM1 was proved to be present on the axons of peripheral nerves. Sensitization with purified GM1 also induced axonal neuropathy, indicating that GM1 was the immunogen in the mixture. A model of human axonal Guillain-Barré syndrome has been established that uses inoculation with a bovine brain ganglioside mixture or isolated GM1. This model may help to clarify the molecular pathogenesis of the syndrome and to develop new treatments for it.

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@article{Yuki2001AnimalMO, title={Animal model of axonal Guillain-Barr{\'e} syndrome induced by sensitization with GM1 ganglioside.}, author={Nobuhiro Yuki and M Yamada and Michiaki Koga and Masaaki Odaka and Keiichiro Susuki and Yoh ichi Tagawa and Seiji Ueda and Tsuyoshi Kasama and Akihiro Ohnishi and S Hayashi and Hiroki Takahashi and Makoto Kamijo and K-i Hirata}, journal={Annals of neurology}, year={2001}, volume={49 6}, pages={712-20} }