The association of the human herpesvirus-6 and MS

Author:

Friedman J E1,Lyons M J2,Cu G2,Ablashl D V3,Whitman J E3,Edgar M4,Koskiniemi Marjaleena5,Vaheri Antti5,Zabriskie J B2

Affiliation:

1. Department of Neurology, NYU Medical Center, New York 10016 USA, Laboratory of Clinical Microbiology and Immunology, The Rockefeller University, 1230 York Avenue, New York 10021 USA

2. Laboratory of Clinical Microbiology and Immunology, The Rockefeller University, 1230 York Avenue, New York 10021 USA

3. Advanced Biotechnologies, Columbia, Maryland 21046 USA

4. Department of Neuropathology New York Hospital-Cornell Medical Center NY, New York 10021, USA

5. Department of Virology, University of Helsinki, Finland

Abstract

Given the clinical and pathological nature of multiple sclerosis (MS), a viral infection has long been hypothesized as part of the etiology. In this study we investigated the possibility that the human herpesvirus-6 (HHV-6) is present in a dormant or active phase in the tissue of MS patients, specifically oligodendrocytes. Using PCR assays of MS and non-MS brain sections with primers prepared against the HHV-6 structural protein 101, the results demonstrated that 36% of MS brains were positive for the virus, while 13.5% of non-MS brains were positive. Antibody to the HHV-6 structural protein was also used in immunohistochemical experiments in brain tissue. 47% (7/15) of MS brains were positive for HHV-6, whereas 0/16 controls were positive. In addition, MS patients demonstrated high immune reactivity to this virus, even when compared to auto-immune diseases, which might cause polyclonal activation. Sera obtained from MS and control patients revealed that the IgM response to the HHV-6 virus was significantly elevated in 80% patients compared to 16% non-MS controls, P5.001. The above experiments strongly suggest that a significant number of MS brain samples contain HHV-6 antigens and genomic fragments in a dormant or active phase compared to control specimens and that MS patients mount a brisk, early IgM response.

Publisher

SAGE Publications

Subject

Clinical Neurology,Neurology

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