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NEUROLOGY 1988;38:1592
© 1988 American Academy of Neurology

Anti-neuroblastoma cell line antibodies in inflammatory demyelinating polyneuropathy

Inhibition in vitro and in vivo by IV immunoglobulin

P. A. van Doorn, MD, A. Brand, MD and M. Vermeulen, MD

Department of Neurology (Drs. van Doom and Vermeulen), Academic Hospital Dijkzigt, Rotterdam; and the Department of Immunohaematology and Bloodbank (Drs. van Doom and Brand), Academic Hospital Leiden, The Netherlands.

We tested serum from 48 patients with Guillain-Barré syndrome and 42 with chronic inflammatory demyelinating polyneuropathy (CIDP) against a selected neuroblastoma cell line (NBL 108cc15). Forty-two percent of the patients showed a positive immunofluorescence test against the NBL 108cc15. These antibodies were mainly of the IgM-class; they disappeared in all seven CIDP patients retested after improvement following intravenous IgG treatment (IV-IgG) and were present in only 5% of serum from patients with other disorders. Absorption studies showed a partial homology between the NBL 108cc15 and human sciatic nerve. In vitro studies showed that IgG from pooled normal donors (IV-IgG) inhibits the reaction between serum from a CIDP patient and the NBL cell line. This inhibition may be due to neutralization of autoantibodies against nervous tissue by anti-idiotypic antibodies in IV-IgG.

Address correspondence and reprint requests to Dr. van Doom, Department of Neurology, Academic Hospital Dijkzigt, Dr. Molewaterplein 40,3015 GD Rotterdam, The Netherlands.

Received February 26, 1988. Accepted for publication in final form April 11, 1988.




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Arch NeurolHome page
M. Stangel, K. V. Toyka, and R. Gold
Mechanisms of High-Dose Intravenous Immunoglobulins in Demyelinating Diseases
Arch Neurol, June 1, 1999; 56(6): 661 - 663.
[Abstract] [Full Text] [PDF]




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