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NEUROLOGY 1981;31:1402
© 1981 American Academy of Neurology

Circulating immune complexes in neurologic disease

Avertano B. C. Noronha, M.D., Jack P. Antel, M.D., Raymond P. Roos, M.D. and M. Edward Medof, M.D., Ph.D.

Departments of Neurology (Drs. Noronha, Antel, and Roos) and Medicine (Dr. Medof), Division of the Biological Sciences, the University of Chicago, and the Pritzker School of Medicine, Chicago, IL.

Address correspondence and reprint requests to Dr. Medof, Department of Medicine, the University of Chicago, 950 E. 59th Street, Box 404, Chicago, IL 60637.

Sera from patients with multiple sclerosis (MS), amyotrophic lateral sclerosis (ALS), subacute sclerosing panencephalitis (SSPE), and myasthenia gravis (MG) were assayed for immune complexes. Three techniques were used: a modified Raji cell assay, the 129-Clq polyethyleneglycol assay, and a solid-phase Clq assay. Immune complex levels were elevated in sera of some patients with MS, ALS, and SSPE, but the elevations were modest when compared with active systemic lupus erythematosus (SLE). In some cases, abnormalities were detected in only one assay system; in other cases, abnormalities were detected by two or three assay systems. In MS, immune complex elevations correlated with active disease and with decreased suppressor cell activity. Of two ALAS patients with antecedent poliomyelitis, one had markedly increased levels of immune complexes in two assays. In MG, levels of immune complexes did not differ from those of controls.




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[Abstract] [Full Text] [PDF]




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