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NEUROLOGY 1980;30:1155
© 1980 American Academy of Neurology

Multiple sclerosis de novo CNS IgG synthesis

Effect of ACTH and corticosteroids

Wallace W. Tourtellotte, M.D., Ph.D., Robert W. Baumhefner, M.D., Alfred R. Potvin, Ph.D., Boce I. Ma, Ph.D., Janet H. Potvin, Ph.D., Mario Mendez, M.D. and Karl Syndulko, Ph.D.

Neurology and Research Services (Drs. Tourtellotte, Baumhefner, Ma, Mendez, and Syndulko), VA Wadsworth Medical Center, Los Angeles; the Department of Neurology, University of California at Los Angeles School of Medicine (Drs. Tourtellotte and Baumhefner); and the University of Texas at Arlington Biomedical Engineering Program (Dr Potvin) and Department of English (Dr. J.H. Potvin).

ACTH gel and corticosteroids were given to 28 clinically definite multiple sclerosis (MS) patients to determine whether de novo central nervous system (CNS) IgG synthesis (rate and cerebrospinal fluid [CSF] IgG oligoclonal bands) could be eradicated. The most effective treatments were ACTH gel and ACTH gel followed by prednisone; all 11 patients had a significant reduction in rate (p < 0.051, which became normal in eight patients (< 3.3 mg per day). In order of effectiveness, the other drugs used were: dexamethasone or prednisone given orally, and hydrocortisone administered intrathecally. For most treatments, reduction of the rate of CNS IgG synthesis occurred within days and persisted for months after cessation of treatment. The MS CNS immune reaction was not eradicated when IgG synthesis rate became normal, because CSF IgG oligoelonal bands persisted. None of the chronic progressive, severely disabled patients demonstrated significant change in neurologic function or persistent adverse effects.

Address correspondence and reprint requests to Dr. Tourtellotte, Chief, Neurology Service, VA Wadsworth Medical Center, Wilshire and Sawtelle Blvds., Los Angeles, CA 90073.

Accepted for publication January 18, 1980

This research was supported in part by the VA Medical Research Funds, the National Multiple Sclerosis Society, the Kroc Foundation for Advancement of Medical Science, the Upjohn Company, and the University of Texas at Arlington Organized Research Funds.




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