Measles Inclusion-Body Encephalitis Caused by the Vaccine Strain of Measles Virus

We report a case of measles inclusion-body encephalitis (MIBE) occurring in an apparently healthy 21-month-old boy 8.5 months after measles-mumps-rubella vaccination. He had no prior evidence of immune deficiency and no history of measles exposure or clinical disease. During hospitalization, a prima...

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Published inClinical infectious diseases Vol. 29; no. 4; pp. 855 - 861
Main Authors Bitnun, Ari, Shannon, Patrick, Durward, Andrew, Rota, Paul A., Bellini, William J., Graham, Caroline, Wang, Elaine, Ford-Jones, Elizabeth L., Cox, Peter, Becker, Laurence, Fearon, Margaret, Petric, Martin, Tellier, Raymond
Format Journal Article Conference Proceeding
LanguageEnglish
Published Chicago, IL The University of Chicago Press 01.10.1999
University of Chicago Press
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Summary:We report a case of measles inclusion-body encephalitis (MIBE) occurring in an apparently healthy 21-month-old boy 8.5 months after measles-mumps-rubella vaccination. He had no prior evidence of immune deficiency and no history of measles exposure or clinical disease. During hospitalization, a primary immunodeficiency characterized by a profoundly depressed CD8 cell count and dysgammaglobulinemia was demonstrated. A brain biopsy revealed histopathologic features consistent with MIBE, and measles antigens were detected by immunohistochemical staining. Electron microscopy revealed inclusions characteristic of paramyxovirus nucleocapsids within neurons, oligodendroglia, and astrocytes. The presence of measles virus in the brain tissue was confirmed by reverse transcription polymerase chain reaction. The nucleotide sequence in the nucleoprotein and fusion gene regions was identical to that of the Moraten and Schwarz vaccine strains; the fusion gene differed from known genotype A wild-type viruses.
Bibliography:istex:4DF21D9141EA9B150285DFC2AFF5A908F710071E
ark:/67375/HXZ-QSVNHS05-H
Current affiliations: Dr. Patrick Shannon, Department of Pathology and Laboratory Medicine, Division of Neuropathology, The Toronto Hospital, Western Division, The University of Toronto, Toronto, Ontario, Canada; Dr. Andrew Durward, Department of Paediatric Intensive Care Medicine, Guy's Hospital, London, England.
Reprints or correspondence: Dr. Raymond Tellier, Division of Microbiology, The Hospital for Sick Children, 555 University Avenue, Toronto, Ontario M5G 1X8, Canada (raymond.tellier@sickkids.on.ca).
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ISSN:1058-4838
1537-6591
DOI:10.1086/520449