Deficiency of the complement regulator CD59a enhances disease severity, demyelination and axonal injury in murine acute experimental allergic encephalomyelitis

R. J. Mead, J. W. Neal, M. R. Griffiths, Christopher Linington, M. Botto, H. Lassmann, B. P. Morgan

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    Abstract

    There is a growing body of evidence implicating complement and, in particular, the terminal pathway ( membrane attack complex; MAC) in inducing demyelination in multiple sclerosis and experimental allergic encephalomyelitis. In this paper, we examined the disease course and pathological changes in mice deficient in the major regulator of MAC assembly, CD59a, during the course of acute experimental allergic encephalomyelitis induced by immunisation with recombinant myelin oligodendrocyte glycoprotein. Disease incidence and severity were significantly increased in CD59a-deficient mice. The extent of inflammation, demyelination and axonal injury were assessed in spinal cord cross-sections from CD59a- deficient and control mice, and all these parameters were enhanced in the absence of CD59a. Areas of myelin loss and axonal damage in CD59a-deficient mice were associated with deposits of MAC, firmly implicating MAC as a cause of the observed injury. These findings are relevant to some types of human demyelination, where abundant deposits of MAC are found in association with pathology.

    Original languageEnglish
    Pages (from-to)21-28
    Number of pages7
    JournalLaboratory Investigation
    Volume84
    DOIs
    Publication statusPublished - 2004

    Keywords

    • complement
    • CD59
    • knockout
    • demyelination
    • encephalomyelitis
    • MYELIN OLIGODENDROCYTE GLYCOPROTEIN
    • EXPERIMENTAL AUTOIMMUNE ENCEPHALOMYELITIS
    • PAROXYSMAL-NOCTURNAL HEMOGLOBINURIA
    • MULTIPLE-SCLEROSIS
    • FUNCTIONAL-CHARACTERIZATION
    • MEDIATED DEMYELINATION
    • MONOCLONAL-ANTIBODIES
    • TISSUE DISTRIBUTION
    • EXPRESSION
    • MICE

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